Running 'testthat.R' [118s]
Running the tests in 'tests/testthat.R' failed.
Complete output:
  > library(testthat)
  > library(loose.rock)
  > 
  > test_check("loose.rock")
  additional arguments ignored in warning()
  additional arguments ignored in warning()
  [ FAIL 2 | WARN 0 | SKIP 2 | PASS 218 ]
  
  == Skipped tests ===============================================================
  * empty test (2)
  
  == Failed tests ================================================================
  -- Error (test-coding.genes.R:137:5): getBM multiple combinations of useCache --
  Error in `(function (attributes, filters = "", values = "", mart, curl = NULL, 
      checkFilters = TRUE, verbose = FALSE, uniqueRows = TRUE, 
      bmHeader = FALSE, quote = "\"", useCache = TRUE) 
  {
      martCheck(mart)
      if (missing(attributes)) 
          stop("Argument 'attributes' must be specified.")
      if (is.list(filters) && !missing(values)) 
          warning("Argument 'values' should not be used when argument 'filters' is a list and will be ignored.")
      if (is.list(filters) && is.null(names(filters))) 
          stop("Argument 'filters' must be a named list when sent as a list.")
      if (!is.list(filters) && all(filters != "") && missing(values)) 
          stop("Argument 'values' must be specified.")
      if (length(filters) > 0 && length(values) == 0) 
          stop("Values argument contains no data.")
      if (is.list(filters)) {
          values = filters
          filters = names(filters)
      }
      if (class(uniqueRows) != "logical") 
          stop("Argument 'uniqueRows' must be a logical value, so either TRUE or FALSE")
      if (useCache) {
          cache <- Sys.getenv(x = "BIOMART_CACHE", unset = rappdirs::user_cache_dir(appname = "biomaRt"))
          bfc <- BiocFileCache::BiocFileCache(cache, ask = FALSE)
      }
      hash <- .createHash(mart, attributes, filters, values, uniqueRows, 
          bmHeader)
      if (useCache && .checkCache(bfc, hash)) {
          if (verbose) {
              message("Cache found")
          }
          cache_hits <- bfcquery(bfc, hash, field = "rname")
          if (nrow(cache_hits) > 1) {
              stop("Multiple cache results found")
          }
          else {
              rid <- cache_hits$rid
              load(bfc[[rid]])
              return(result)
          }
      }
      else {
          callHeader <- TRUE
          xmlQuery = paste0("<?xml version='1.0' encoding='UTF-8'?><!DOCTYPE Query><Query  virtualSchemaName = '", 
              martVSchema(mart), "' uniqueRows = '", as.numeric(uniqueRows), 
              "' count='0' datasetConfigVersion='0.6' header='", 
              as.numeric(callHeader), "' formatter='TSV' requestid='biomaRt'> <Dataset name = '", 
              martDataset(mart), "'>")
          invalid = !(attributes %in% listAttributes(mart, what = "name"))
          if (any(invalid)) 
              stop(paste("Invalid attribute(s):", paste(attributes[invalid], 
                  collapse = ", "), "\nPlease use the function 'listAttributes' to get valid attribute names"))
          attributeXML = paste("<Attribute name = '", attributes, 
              "'/>", collapse = "", sep = "")
          if (filters[1] != "" && checkFilters) {
              invalid = !(filters %in% listFilters(mart, what = "name"))
              if (any(invalid)) 
                  stop(paste("Invalid filters(s):", paste(filters[invalid], 
                    collapse = ", "), "\nPlease use the function 'listFilters' to get valid filter names"))
          }
          filterXmlList <- .generateFilterXML(filters, values, 
              mart)
          resultList <- list()
          if (length(filterXmlList) > 1) {
              pb <- progress_bar$new(total = length(filterXmlList), 
                  width = options()$width - 10, format = "Batch submitting query [:bar] :percent eta: :eta")
              pb$tick(0)
              on.exit(pb$terminate())
          }
          for (i in seq_along(filterXmlList)) {
              if (i > 1) {
                  pb$tick()
              }
              filterXML <- filterXmlList[[i]]
              fullXmlQuery = paste(xmlQuery, attributeXML, filterXML, 
                  "</Dataset></Query>", sep = "")
              if (verbose) {
                  message(fullXmlQuery)
              }
              sep <- ifelse(grepl(x = martHost(mart), pattern = ".+\\?.+"), 
                  "&", "?")
              chunk_hash <- as(openssl::md5(paste(martHost(mart), 
                  fullXmlQuery)), "character")
              tf <- file.path(tempdir(), paste0("biomaRt_", chunk_hash, 
                  ".rds"))
              if (!file.exists(tf)) {
                  postRes <- .submitQueryXML(host = paste0(martHost(mart), 
                    sep), query = fullXmlQuery)
                  result <- .processResults(postRes, mart = mart, 
                    sep = sep, fullXmlQuery = fullXmlQuery, verbose = verbose, 
                    callHeader = callHeader, quote = quote, attributes = attributes)
                  saveRDS(result, file = tf)
              }
              else {
                  result <- readRDS(tf)
              }
              resultList[[i]] <- .setResultColNames(result, mart = mart, 
                  attributes = attributes, bmHeader = bmHeader)
          }
          result <- do.call("rbind", resultList)
          if (useCache) {
              tf <- tempfile()
              save(result, file = tf)
              bfcadd(bfc, rname = hash, fpath = tf, action = "copy")
              file.remove(tf)
          }
          file.remove(list.files(tempdir(), pattern = "^biomaRt.*rds$", 
              full.names = TRUE))
          return(result)
      }
  })(attributes = c("ensembl_gene_id", "external_gene_name"), filters = "external_gene_name", 
      values = c("BRCA1", "BRCA2", "CHADL", "BTBD8", "BCAS2", "AGAP1"
      ), mart = new("Mart", biomart = "ENSEMBL_MART_ENSEMBL", host = "https://www.ensembl.org:443/biomart/martservice", 
          vschema = "default", version = character(0), dataset = "hsapiens_gene_ensembl", 
          filters = structure(list(name = c("chromosome_name", 
          "start", "end", "strand", "chromosomal_region", "with_biogrid", 
          "with_ccds", "with_chembl", "with_dbass3", "with_dbass5", 
          "with_ens_hs_transcript", "with_ens_hs_translation", 
          "with_entrezgene_trans_name", "with_embl", "with_arrayexpress", 
          "with_genedb", "with_go", "with_goslim_goa", "with_hgnc", 
          "with_hpa", "with_protein_id", "with_ens_lrg_gene", "with_ens_lrg_transcript", 
          "with_merops", "with_mim_gene", "with_mim_morbid", "with_mirbase", 
          "with_mirbase_trans_name", "with_entrezgene", "with_pdb", 
          "with_reactome", "with_reactome_gene", "with_reactome_transcript", 
          "with_refseq_mrna", "with_refseq_mrna_predicted", "with_refseq_ncrna", 
          "with_refseq_ncrna_predicted", "with_refseq_peptide", 
          "with_refseq_peptide_predicted", "with_rfam", "with_rfam_trans_name", 
          "with_rnacentral", "with_hgnc_trans_name", "with_ucsc", 
          "with_uniparc", "with_uniprot_gn", "with_uniprot_isoform", 
          "with_uniprotswissprot", "with_uniprotsptrembl", "with_wikigene", 
          "ensembl_gene_id", "ensembl_gene_id_version", "ensembl_transcript_id", 
          "ensembl_transcript_id_version", "ensembl_peptide_id", 
          "ensembl_peptide_id_version", "ensembl_exon_id", "external_gene_name", 
          "external_transcript_name", "external_synonym", "biogrid", 
          "ccds", "chembl", "dbass3_name", "dbass3_id", "dbass5_name", 
          "dbass5_id", "ens_hs_transcript", "ens_hs_translation", 
          "entrezgene_trans_name", "embl", "arrayexpress", "genedb", 
          "go", "goslim_goa", "hgnc_id", "hgnc_symbol", "hpa_accession", 
          "hpa_id", "protein_id", "ens_lrg_gene", "ens_lrg_transcript", 
          "merops", "mim_gene_accession", "mim_morbid_accession", 
          "mirbase_accession", "mirbase_id", "mirbase_trans_name", 
          "entrezgene_accession", "entrezgene_id", "pdb", "reactome", 
          "reactome_gene", "reactome_transcript", "refseq_mrna", 
          "refseq_mrna_predicted", "refseq_ncrna", "refseq_ncrna_predicted", 
          "refseq_peptide", "refseq_peptide_predicted", "rfam", 
          "rfam_trans_name", "rnacentral", "hgnc_trans_name", "ucsc", 
          "uniparc", "uniprot_gn_symbol", "uniprot_gn_id", "uniprot_isoform", 
          "uniprotswissprot", "uniprotsptrembl", "wikigene_name", 
          "wikigene_id", "with_affy_hc_g110", "with_affy_hg_focus", 
          "with_affy_hg_u133a", "with_affy_hg_u133a_2", "with_affy_hg_u133b", 
          "with_affy_hg_u133_plus_2", "with_affy_hg_u95a", "with_affy_hg_u95av2", 
          "with_affy_hg_u95b", "with_affy_hg_u95c", "with_affy_hg_u95d", 
          "with_affy_hg_u95e", "with_affy_hta_2_0", "with_affy_huex_1_0_st_v2", 
          "with_affy_hugenefl", "with_affy_hugene_1_0_st_v1", "with_affy_hugene_2_0_st_v1", 
          "with_affy_hugene_2_1_st_v1", "with_affy_primeview", 
          "with_affy_u133_x3p", "with_agilent_cgh_44b", "with_agilent_gpl26966", 
          "with_agilent_gpl6848", "with_agilent_sureprint_g3_ge_8x60k", 
          "with_agilent_sureprint_g3_ge_8x60k_v2", "with_agilent_wholegenome", 
          "with_agilent_wholegenome_4x44k_v1", "with_agilent_wholegenome_4x44k_v2", 
          "with_codelink_codelink", "with_illumina_humanht_12_v3", 
          "with_illumina_humanht_12_v4", "with_illumina_humanref_8_v3", 
          "with_illumina_humanwg_6_v1", "with_illumina_humanwg_6_v2", 
          "with_illumina_humanwg_6_v3", "with_phalanx_onearray", 
          "affy_hc_g110", "affy_hg_focus", "affy_hg_u133a", "affy_hg_u133a_2", 
          "affy_hg_u133b", "affy_hg_u133_plus_2", "affy_hg_u95a", 
          "affy_hg_u95av2", "affy_hg_u95b", "affy_hg_u95c", "affy_hg_u95d", 
          "affy_hg_u95e", "affy_hta_2_0", "affy_huex_1_0_st_v2", 
          "affy_hugenefl", "affy_hugene_1_0_st_v1", "affy_hugene_2_0_st_v1", 
          "affy_hugene_2_1_st_v1", "affy_primeview", "affy_u133_x3p", 
          "agilent_cgh_44b", "agilent_gpl26966", "agilent_gpl6848", 
          "agilent_sureprint_g3_ge_8x60k", "agilent_sureprint_g3_ge_8x60k_v2", 
          "agilent_wholegenome", "agilent_wholegenome_4x44k_v1", 
          "agilent_wholegenome_4x44k_v2", "codelink_codelink", 
          "illumina_humanht_12_v3", "illumina_humanht_12_v4", "illumina_humanref_8_v3", 
          "illumina_humanwg_6_v1", "illumina_humanwg_6_v2", "illumina_humanwg_6_v3", 
          "phalanx_onearray", "transcript_count_greater_than", 
          "transcript_count_less_than", "biotype", "transcript_biotype", 
          "source", "transcript_source", "transcript_tsl", "transcript_gencode_basic", 
          "transcript_appris", "transcript_is_canonical", "mane_select", 
          "mane_plus_clinical", "phenotype_description", "phenotype_source", 
          "go_parent_term", "go_parent_name", "go_evidence_code", 
          "with_hsapiens_paralog", "with_cabingdonii_homolog", 
          "with_scaustralis_homolog", "with_mspretus_homolog", 
          "with_vpacos_homolog", "with_mmmarmota_homolog", "with_pformosa_homolog", 
          "with_bbbison_homolog", "with_uamericanus_homolog", "with_nvison_homolog", 
          "with_cdromedarius_homolog", "with_uparryii_homolog", 
          "with_smerianae_homolog", "with_dnovemcinctus_homolog", 
          "with_sformosus_homolog", "with_gmorhua_homolog", "with_charengus_homolog", 
          "with_ssalar_homolog", "with_cporosus_homolog", "with_lbergylta_homolog", 
          "with_lcalcarifer_homolog", "with_dleucas_homolog", "with_spartitus_homolog", 
          "with_rbieti_homolog", "with_bmusculus_homolog", "with_llaticaudata_homolog", 
          "with_sbboliviensis_homolog", "with_ppaniscus_homolog", 
          "with_strutta_homolog", "with_hburtoni_homolog", "with_ogarnettii_homolog", 
          "with_cintestinalis_homolog", "with_csavignyi_homolog", 
          "with_celegans_homolog", "with_ccapucinus_homolog", "with_fcatus_homolog", 
          "with_cwagneri_homolog", "with_cgobio_homolog", "with_ipunctatus_homolog", 
          "with_ggallus_homolog", "with_ptroglodytes_homolog", 
          "with_cgchok1gshd_homolog", "with_osinensis_homolog", 
          "with_psinensis_homolog", "with_otshawytscha_homolog", 
          "with_atestudineus_homolog", "with_aocellaris_homolog", 
          "with_lchalumnae_homolog", "with_okisutch_homolog", "with_falbicollis_homolog", 
          "with_scanaria_homolog", "with_ccarpio_homolog", "with_pmuralis_homolog", 
          "with_vursinus_homolog", "with_pcoquereli_homolog", "with_btaurus_homolog", 
          "with_mfascicularis_homolog", "with_odegus_homolog", 
          "with_dclupeoides_homolog", "with_cldingo_homolog", "with_clfamiliaris_homolog", 
          "with_ttruncatus_homolog", "with_bgrunniens_homolog", 
          "with_eaasinus_homolog", "with_mleucophaeus_homolog", 
          "with_dmelanogaster_homolog", "with_applatyrhynchos_homolog", 
          "with_ptextilis_homolog", "with_acalliptera_homolog", 
          "with_eelectricus_homolog", "with_lafricana_homolog", 
          "with_cmilii_homolog", "with_svulgaris_homolog", "with_dlabrax_homolog", 
          "with_mpfuro_homolog", "with_trubripes_homolog", "with_amelanoleuca_homolog", 
          "with_nleucogenys_homolog", "with_saurata_homolog", "with_chircus_homolog", 
          "with_mauratus_homolog", "with_acchrysaetos_homolog", 
          "with_rroxellana_homolog", "with_sgrahami_homolog", "with_cauratus_homolog", 
          "with_gevgoodei_homolog", "with_ggorilla_homolog", "with_pmajor_homolog", 
          "with_sdumerili_homolog", "with_psimus_homolog", "with_rferrumequinum_homolog", 
          "with_acarolinensis_homolog", "with_cporcellus_homolog", 
          "with_preticulata_homolog", "with_eburgeri_homolog", 
          "with_eeuropaeus_homolog", "with_ecaballus_homolog", 
          "with_hhucho_homolog", "with_bihybrid_homolog", "with_pcapensis_homolog", 
          "with_nnaja_homolog", "with_omelastigma_homolog", "with_olatipes_homolog", 
          "with_cjaponica_homolog", "with_ojavanicus_homolog", 
          "with_shabroptila_homolog", "with_dordii_homolog", "with_pcinereus_homolog", 
          "with_pmarinus_homolog", "with_lcrocea_homolog", "with_lleishanense_homolog", 
          "with_ppardus_homolog", "with_jjaculus_homolog", "with_etelfairi_homolog", 
          "with_pleo_homolog", "with_clanigera_homolog", "with_clumpus_homolog", 
          "with_nbrichardi_homolog", "with_anancymaae_homolog", 
          "with_mmulatta_homolog", "with_nscutatus_homolog", "with_pnyererei_homolog", 
          "with_kmarmoratus_homolog", "with_gfortis_homolog", "with_pvampyrus_homolog", 
          "with_amexicanus_homolog", "with_mlucifugus_homolog", 
          "with_acitrinellus_homolog", "with_mmusculus_homolog", 
          "with_mmurinus_homolog", "with_fheteroclitus_homolog", 
          "with_hgfemale_homolog", "with_mmonoceros_homolog", "with_oniloticus_homolog", 
          "with_pmbairdii_homolog", "with_elucius_homolog", "with_panubis_homolog", 
          "with_mdomestica_homolog", "with_apercula_homolog", "with_cpbellii_homolog", 
          "with_pkingsleyae_homolog", "with_sscrofa_homolog", "with_mnemestrina_homolog", 
          "with_oprinceps_homolog", "with_slucioperca_homolog", 
          "with_mmurdjan_homolog", "with_abrachyrhynchus_homolog", 
          "with_xmaculatus_homolog", "with_oanatinus_homolog", 
          "with_umaritimus_homolog", "with_mochrogaster_homolog", 
          "with_ocuniculus_homolog", "with_omykiss_homolog", "with_rnorvegicus_homolog", 
          "with_vvulpes_homolog", "with_pnattereri_homolog", "with_ecalabaricus_homolog", 
          "with_mcaroli_homolog", "with_scerevisiae_homolog", "with_platipinna_homolog", 
          "with_oarambouillet_homolog", "with_cvariegatus_homolog", 
          "with_saraneus_homolog", "with_mpahari_homolog", "with_bsplendens_homolog", 
          "with_mmoschiferus_homolog", "with_choffmanni_homolog", 
          "with_catys_homolog", "with_pcatodon_homolog", "with_apolyacanthus_homolog", 
          "with_loculatus_homolog", "with_itridecemlineatus_homolog", 
          "with_mspicilegus_homolog", "with_gaculeatus_homolog", 
          "with_pabelii_homolog", "with_csyrichta_homolog", "with_sharrisii_homolog", 
          "with_tnigroviridis_homolog", "with_tctriunguis_homolog", 
          "with_ptaltaica_homolog", "with_hcomes_homolog", "with_csemilaevis_homolog", 
          "with_tbelangeri_homolog", "with_xtropicalis_homolog", 
          "with_spunctatus_homolog", "with_smaximus_homolog", "with_mgallopavo_homolog", 
          "with_nfurzeri_homolog", "with_ngalili_homolog", "with_psinus_homolog", 
          "with_csabaeus_homolog", "with_neugenii_homolog", "with_cjacchus_homolog", 
          "with_bmutus_homolog", "with_chyarkandensis_homolog", 
          "with_sldorsalis_homolog", "with_tguttata_homolog", "with_mzebra_homolog", 
          "with_drerio_homolog", "with_marmatus_homolog", "with_interpro", 
          "with_cdd", "with_gene3d", "with_hamap", "with_mobidblite", 
          "with_ncoils", "with_hmmpanther", "with_pfam", "with_pirsf", 
          "with_prints", "with_scanprosite", "with_pfscan", "with_seg", 
          "with_sfld", "with_sifts_import", "with_signalp", "with_smart", 
          "with_superfamily", "with_tigrfam", "with_tmhmm", "interpro", 
          "cdd", "gene3d", "hamap", "hmmpanther", "pfam", "pirsf", 
          "prints", "scanprosite", "pfscan", "sfld", "smart", "superfamily", 
          "tigrfam", "germ_line_variation_source", "with_validated_snp", 
          "so_mini_parent_name"), description = c("Chromosome/scaffold name", 
          "Start", "End", "Strand", "e.g. 1:100:10000:-1, 1:100000:200000:1", 
          "With BioGRID Interaction data, The General Repository for Interaction Datasets ID(s)", 
          "With CCDS ID(s)", "With ChEMBL ID(s)", "With DataBase of Aberrant 3' Splice Sites ID(s)", 
          "With DataBase of Aberrant 5' Splice Sites ID(s)", "With Ensembl Human Transcript ID(s)", 
          "With Ensembl Human Translation ID(s)", "With EntrezGene transcript name ID(s)", 
          "With European Nucleotide Archive ID(s)", "With Expression Atlas ID(s)", 
          "With GeneDB ID(s)", "With GO ID(s)", "With GOSlim GOA ID(s)", 
          "With HGNC Symbol ID(s)", "With Human Protein Atlas ID(s)", 
          "With INSDC protein ID ID(s)", "With LRG display in Ensembl gene ID(s)", 
          "With LRG display in Ensembl transcript ID(s)", "With MEROPS - the Peptidase Database ID(s)", 
          "With MIM gene ID(s)", "With MIM morbid ID(s)", "With miRBase ID(s)", 
          "With miRBase transcript name ID(s)", "With NCBI gene (formerly Entrezgene) ID(s)", 
          "With PDB ID(s)", "With Reactome ID(s)", "With Reactome gene ID(s)", 
          "With Reactome transcript ID(s)", "With RefSeq mRNA ID(s)", 
          "With RefSeq mRNA predicted ID(s)", "With RefSeq ncRNA ID(s)", 
          "With RefSeq ncRNA predicted ID(s)", "With RefSeq peptide ID(s)", 
          "With RefSeq peptide predicted ID(s)", "With RFAM ID(s)", 
          "With RFAM transcript name ID(s)", "With RNAcentral ID(s)", 
          "With Transcript name ID(s)", "With UCSC Stable ID ID(s)", 
          "With UniParc ID(s)", "With UniProtKB Gene Name ID(s)", 
          "With UniProtKB isoform ID(s)", "With UniProtKB/Swiss-Prot ID(s)", 
          "With UniProtKB/TrEMBL ID(s)", "With WikiGene ID(s)", 
          "Gene stable ID(s) [e.g. ENSG00000000003]", "Gene stable ID(s) with version [e.g. ENSG00000000003.15]", 
          "Transcript stable ID(s) [e.g. ENST00000000233]", "Transcript stable ID(s) with version [e.g. ENST00000000233.10]", 
          "Protein stable ID(s) [e.g. ENSP00000000233]", "Protein stable ID(s) with version [e.g. ENSP00000000233.5]", 
          "Exon ID(s) [e.g. ENSE00000000003]", "Gene Name(s) [e.g. MT-TF]", 
          "Transcript Name(s) [e.g. MT-TF-201]", "Gene Synonym(s) [e.g. 0808y08y]", 
          "BioGRID Interaction data, The General Repository for Interaction Datasets ID(s) [e.g. 106523]", 
          "CCDS ID(s) [e.g. CCDS10]", "ChEMBL ID(s) [e.g. CHEMBL1075092]", 
          "DataBase of Aberrant 3' Splice Sites name(s) [e.g. ABCR ]", 
          "DataBase of Aberrant 3' Splice Sites ID(s) [e.g. 1]", 
          "DataBase of Aberrant 5' Splice Sites name(s) [e.g. BRCA1]", 
          "DataBase of Aberrant 5' Splice Sites ID(s) [e.g. 382]", 
          "Ensembl Human Transcript ID(s) [e.g. ENST00000009180]", 
          "Ensembl Human Translation ID(s) [e.g. ENSP00000009180]", 
          "EntrezGene transcript name ID(s) [e.g. AA06-201]", "European Nucleotide Archive ID(s) [e.g. A06800]", 
          "Expression Atlas ID(s) [e.g. ENSG00000000003]", "GeneDB ID(s) [e.g. Smp_009580.1:pep]", 
          "GO ID(s) [e.g. GO:0000002]", "GOSlim GOA ID(s) [e.g. GO:0000003]", 
          "HGNC ID(s) [e.g. HGNC:100]", "HGNC symbol(s) [e.g. A1BG]", 
          "Human Protein Atlas accession(s) [e.g. CAB000001]", 
          "Human Protein Atlas ID(s) [e.g. 1]", "INSDC protein ID(s) [e.g. AAA02489]", 
          "LRG display in Ensembl gene ID(s) [e.g. LRG_1]", "LRG display in Ensembl transcript ID(s) [e.g. LRG_1000t1]", 
          "MEROPS - the Peptidase Database ID(s) [e.g. A01.001]", 
          "MIM gene accession(s) [e.g. 100640]", "MIM morbid accession(s) [e.g. 100100]", 
          "miRBase accession(s) [e.g. MI0000060]", "miRBase ID(s) [e.g. hsa-let-7a-1]", 
          "miRBase transcript name ID(s) [e.g. hsa-mir-1253.1-201]", 
          "NCBI gene (formerly Entrezgene) accession(s) [e.g. A1BG]", 
          "NCBI gene (formerly Entrezgene) ID(s) [e.g. 1]", "PDB ID(s) [e.g. 10GS]", 
          "Reactome ID(s) [e.g. R-HSA-1059683]", "Reactome gene ID(s) [e.g. R-HSA-1059683]", 
          "Reactome transcript ID(s) [e.g. R-HSA-1059683]", "RefSeq mRNA ID(s) [e.g. NM_000014]", 
          "RefSeq mRNA predicted ID(s) [e.g. XM_003118719]", "RefSeq ncRNA ID(s) [e.g. NR_000005]", 
          "RefSeq ncRNA predicted ID(s) [e.g. XR_001736900]", "RefSeq peptide ID(s) [e.g. NP_000005]", 
          "RefSeq peptide predicted ID(s) [e.g. XP_003118767]", 
          "RFAM ID(s) [e.g. RF00001]", "RFAM transcript name ID(s) [e.g. 5S_rRNA.1-201]", 
          "RNAcentral ID(s) [e.g. URS0000000055]", "Transcript name ID(s) [e.g. A1BG-201]", 
          "UCSC Stable ID(s) [e.g. uc001aak.4]", "UniParc ID(s) [e.g. UPI000000003C]", 
          "UniProtKB Gene Name symbol(s) [e.g. 5HT1A]", "UniProtKB Gene Name ID(s) [e.g. A0A023T6R1]", 
          "UniProtKB isoform ID(s) [e.g. A0A096LP49-1]", "UniProtKB/Swiss-Prot ID(s) [e.g. A0A024RBG1]", 
          "UniProtKB/TrEMBL ID(s) [e.g. A0A023T6R1]", "WikiGene name(s) [e.g. A1BG]", 
          "WikiGene ID(s) [e.g. 1]", "With AFFY HC G110 probe ID(s)", 
          "With AFFY HG Focus probe ID(s)", "With AFFY HG U133A probe ID(s)", 
          "With AFFY HG U133A 2 probe ID(s)", "With AFFY HG U133B probe ID(s)", 
          "With AFFY HG U133 Plus 2 probe ID(s)", "With AFFY HG U95A probe ID(s)", 
          "With AFFY HG U95Av2 probe ID(s)", "With AFFY HG U95B probe ID(s)", 
          "With AFFY HG U95C probe ID(s)", "With AFFY HG U95D probe ID(s)", 
          "With AFFY HG U95E probe ID(s)", "With AFFY HTA 2 0 probe ID(s)", 
          "With AFFY HuEx 1 0 st v2 probe ID(s)", "With AFFY HuGeneFL probe ID(s)", 
          "With AFFY HuGene 1 0 st v1 probe ID(s)", "With AFFY HuGene 2 0 st v1 probe ID(s)", 
          "With AFFY HuGene 2 1 st v1 probe ID(s)", "With AFFY PrimeView probe ID(s)", 
          "With AFFY U133 X3P probe ID(s)", "With AGILENT CGH 44b probe ID(s)", 
          "With AGILENT GPL26966 probe ID(s)", "With AGILENT GPL6848 probe ID(s)", 
          "With AGILENT SurePrint G3 GE 8x60k probe ID(s)", "With AGILENT SurePrint G3 GE 8x60k v2 probe ID(s)", 
          "With AGILENT WholeGenome probe ID(s)", "With AGILENT WholeGenome 4x44k v1 probe ID(s)", 
          "With AGILENT WholeGenome 4x44k v2 probe ID(s)", "With CODELINK CODELINK probe ID(s)", 
          "With ILLUMINA HumanHT 12 V3 probe ID(s)", "With ILLUMINA HumanHT 12 V4 probe ID(s)", 
          "With ILLUMINA HumanRef 8 V3 probe ID(s)", "With ILLUMINA HumanWG 6 V1 probe ID(s)", 
          "With ILLUMINA HumanWG 6 V2 probe ID(s)", "With ILLUMINA HumanWG 6 V3 probe ID(s)", 
          "With PHALANX OneArray probe ID(s)", "AFFY HC G110 probe ID(s) [e.g. 737_at]", 
          "AFFY HG Focus probe ID(s) [e.g. 220771_at]", "AFFY HG U133A probe ID(s) [e.g. 211600_at]", 
          "AFFY HG U133A 2 probe ID(s) [e.g. 211600_at]", "AFFY HG U133B probe ID(s) [e.g. 224373_s_at]", 
          "AFFY HG U133 Plus 2 probe ID(s) [e.g. 1553551_s_at]", 
          "AFFY HG U95A probe ID(s) [e.g. 34279_at]", "AFFY HG U95Av2 probe ID(s) [e.g. 34279_at]", 
          "AFFY HG U95B probe ID(s) [e.g. 49072_at]", "AFFY HG U95C probe ID(s) [e.g. 66072_at]", 
          "AFFY HG U95D probe ID(s) [e.g. 76451_at]", "AFFY HG U95E probe ID(s) [e.g. 88289_at]", 
          "AFFY HTA 2 0 probe ID(s) [e.g. TC0M000002.hg]", "AFFY HuEx 1 0 st v2 probe ID(s) [e.g. 2864632]", 
          "AFFY HuGeneFL probe ID(s) [e.g. Z70759_at]", "AFFY HuGene 1 0 st v1 probe ID(s) [e.g. 7946563]", 
          "AFFY HuGene 2 0 st v1 probe ID(s) [e.g. 17100641]", 
          "AFFY HuGene 2 1 st v1 probe ID(s) [e.g. 17100639]", 
          "AFFY PrimeView probe ID(s) [e.g. 11761515_s_at]", "AFFY U133 X3P probe ID(s) [e.g. 1553551_3p_s_at]", 
          "AGILENT CGH 44b probe ID(s) [e.g. A_14_P135019]", "AGILENT GPL26966 probe ID(s) [e.g. HMNXSV003012672]", 
          "AGILENT GPL6848 probe ID(s) [e.g. A_24_P918875]", "AGILENT SurePrint G3 GE 8x60k probe ID(s) [e.g. A_24_P182122]", 
          "AGILENT SurePrint G3 GE 8x60k v2 probe ID(s) [e.g. A_24_P182122]", 
          "AGILENT WholeGenome probe ID(s) [e.g. A_24_P918875]", 
          "AGILENT WholeGenome 4x44k v1 probe ID(s) [e.g. A_24_P918875]", 
          "AGILENT WholeGenome 4x44k v2 probe ID(s) [e.g. A_24_P182122]", 
          "CODELINK CODELINK probe ID(s) [e.g. GE84207]", "ILLUMINA HumanHT 12 V3 probe ID(s) [e.g. ILMN_1779625]", 
          "ILLUMINA HumanHT 12 V4 probe ID(s) [e.g. ILMN_3308961]", 
          "ILLUMINA HumanRef 8 V3 probe ID(s) [e.g. ILMN_2295987]", 
          "ILLUMINA HumanWG 6 V1 probe ID(s) [e.g. 0005910053]", 
          "ILLUMINA HumanWG 6 V2 probe ID(s) [e.g. ILMN_1779625]", 
          "ILLUMINA HumanWG 6 V3 probe ID(s) [e.g. ILMN_1779625]", 
          "PHALANX OneArray probe ID(s) [e.g. PH_hs_0033947]", 
          "Transcript count >=", "Transcript count <=", "Type", 
          "Transcript Type", "Source (gene)", "Source (transcript)", 
          "Transcript Support Level (TSL)", "GENCODE basic annotation", 
          "APPRIS annotation", "Ensembl Canonical", "MANE Select transcript", 
          "MANE Plus clinical", "Phenotype description", "Phenotype source", 
          "Parent term accession", "Parent term name", "GO Evidence code", 
          "Paralogous Human Genes", "Orthologous Abingdon island giant tortoise Genes", 
          "Orthologous African ostrich Genes", "Orthologous Algerian mouse Genes", 
          "Orthologous Alpaca Genes", "Orthologous Alpine marmot Genes", 
          "Orthologous Amazon molly Genes", "Orthologous American bison Genes", 
          "Orthologous American black bear Genes", "Orthologous American mink Genes", 
          "Orthologous Arabian camel Genes", "Orthologous Arctic ground squirrel Genes", 
          "Orthologous Argentine black and white tegu Genes", "Orthologous Armadillo Genes", 
          "Orthologous Asian bonytongue Genes", "Orthologous Atlantic cod Genes", 
          "Orthologous Atlantic herring Genes", "Orthologous Atlantic salmon Genes", 
          "Orthologous Australian saltwater crocodile Genes", "Orthologous Ballan wrasse Genes", 
          "Orthologous Barramundi perch Genes", "Orthologous Beluga whale Genes", 
          "Orthologous Bicolor damselfish Genes", "Orthologous Black snub-nosed monkey Genes", 
          "Orthologous Blue whale Genes", "Orthologous Blue-ringed sea krait Genes", 
          "Orthologous Bolivian squirrel monkey Genes", "Orthologous Bonobo Genes", 
          "Orthologous Brown trout Genes", "Orthologous Burton's mouthbrooder Genes", 
          "Orthologous Bushbaby Genes", "Orthologous C.intestinalis Genes", 
          "Orthologous C.savignyi Genes", "Orthologous Caenorhabditis elegans Genes", 
          "Orthologous Capuchin Genes", "Orthologous Cat Genes", 
          "Orthologous Chacoan peccary Genes", "Orthologous Channel bull blenny Genes", 
          "Orthologous Channel catfish Genes", "Orthologous Chicken Genes", 
          "Orthologous Chimpanzee Genes", "Orthologous Chinese hamster CHOK1GS Genes", 
          "Orthologous Chinese medaka Genes", "Orthologous Chinese softshell turtle Genes", 
          "Orthologous Chinook salmon Genes", "Orthologous Climbing perch Genes", 
          "Orthologous Clown anemonefish Genes", "Orthologous Coelacanth Genes", 
          "Orthologous Coho salmon Genes", "Orthologous Collared flycatcher Genes", 
          "Orthologous Common canary Genes", "Orthologous Common carp Genes", 
          "Orthologous Common wall lizard Genes", "Orthologous Common wombat Genes", 
          "Orthologous Coquerel's sifaka Genes", "Orthologous Cow Genes", 
          "Orthologous Crab-eating macaque Genes", "Orthologous Degu Genes", 
          "Orthologous Denticle herring Genes", "Orthologous Dingo Genes", 
          "Orthologous Dog Genes", "Orthologous Dolphin Genes", 
          "Orthologous Domestic yak Genes", "Orthologous Donkey Genes", 
          "Orthologous Drill Genes", "Orthologous Drosophila melanogaster Genes", 
          "Orthologous Duck Genes", "Orthologous Eastern brown snake Genes", 
          "Orthologous Eastern happy Genes", "Orthologous Electric eel Genes", 
          "Orthologous Elephant Genes", "Orthologous Elephant shark Genes", 
          "Orthologous Eurasian red squirrel Genes", "Orthologous European seabass Genes", 
          "Orthologous Ferret Genes", "Orthologous Fugu Genes", 
          "Orthologous Giant panda Genes", "Orthologous Gibbon Genes", 
          "Orthologous Gilthead seabream Genes", "Orthologous Goat Genes", 
          "Orthologous Golden Hamster Genes", "Orthologous Golden eagle Genes", 
          "Orthologous Golden snub-nosed monkey Genes", "Orthologous Golden-line barbel Genes", 
          "Orthologous Goldfish Genes", "Orthologous Goodes thornscrub tortoise Genes", 
          "Orthologous Gorilla Genes", "Orthologous Great Tit Genes", 
          "Orthologous Greater amberjack Genes", "Orthologous Greater bamboo lemur Genes", 
          "Orthologous Greater horseshoe bat Genes", "Orthologous Green anole Genes", 
          "Orthologous Guinea Pig Genes", "Orthologous Guppy Genes", 
          "Orthologous Hagfish Genes", "Orthologous Hedgehog Genes", 
          "Orthologous Horse Genes", "Orthologous Huchen Genes", 
          "Orthologous Hybrid - Bos Indicus Genes", "Orthologous Hyrax Genes", 
          "Orthologous Indian cobra Genes", "Orthologous Indian medaka Genes", 
          "Orthologous Japanese medaka HdrR Genes", "Orthologous Japanese quail Genes", 
          "Orthologous Javanese ricefish Genes", "Orthologous Kakapo Genes", 
          "Orthologous Kangaroo rat Genes", "Orthologous Koala Genes", 
          "Orthologous Lamprey Genes", "Orthologous Large yellow croaker Genes", 
          "Orthologous Leishan spiny toad Genes", "Orthologous Leopard Genes", 
          "Orthologous Lesser Egyptian jerboa Genes", "Orthologous Lesser hedgehog tenrec Genes", 
          "Orthologous Lion Genes", "Orthologous Long-tailed chinchilla Genes", 
          "Orthologous Lumpfish Genes", "Orthologous Lyretail cichlid Genes", 
          "Orthologous Ma's night monkey Genes", "Orthologous Macaque Genes", 
          "Orthologous Mainland tiger snake Genes", "Orthologous Makobe Island cichlid Genes", 
          "Orthologous Mangrove rivulus Genes", "Orthologous Medium ground-finch Genes", 
          "Orthologous Megabat Genes", "Orthologous Mexican tetra Genes", 
          "Orthologous Microbat Genes", "Orthologous Midas cichlid Genes", 
          "Orthologous Mouse Genes", "Orthologous Mouse Lemur Genes", 
          "Orthologous Mummichog Genes", "Orthologous Naked mole-rat female Genes", 
          "Orthologous Narwhal Genes", "Orthologous Nile tilapia Genes", 
          "Orthologous Northern American deer mouse Genes", "Orthologous Northern pike Genes", 
          "Orthologous Olive baboon Genes", "Orthologous Opossum Genes", 
          "Orthologous Orange clownfish Genes", "Orthologous Painted turtle Genes", 
          "Orthologous Paramormyrops kingsleyae Genes", "Orthologous Pig Genes", 
          "Orthologous Pig-tailed macaque Genes", "Orthologous Pika Genes", 
          "Orthologous Pike-perch Genes", "Orthologous Pinecone soldierfish Genes", 
          "Orthologous Pink-footed goose Genes", "Orthologous Platyfish Genes", 
          "Orthologous Platypus Genes", "Orthologous Polar bear Genes", 
          "Orthologous Prairie vole Genes", "Orthologous Rabbit Genes", 
          "Orthologous Rainbow trout Genes", "Orthologous Rat Genes", 
          "Orthologous Red fox Genes", "Orthologous Red-bellied piranha Genes", 
          "Orthologous Reedfish Genes", "Orthologous Ryukyu mouse Genes", 
          "Orthologous Saccharomyces cerevisiae Genes", "Orthologous Sailfin molly Genes", 
          "Orthologous Sheep Genes", "Orthologous Sheepshead minnow Genes", 
          "Orthologous Shrew Genes", "Orthologous Shrew mouse Genes", 
          "Orthologous Siamese fighting fish Genes", "Orthologous Siberian musk deer Genes", 
          "Orthologous Sloth Genes", "Orthologous Sooty mangabey Genes", 
          "Orthologous Sperm whale Genes", "Orthologous Spiny chromis Genes", 
          "Orthologous Spotted gar Genes", "Orthologous Squirrel Genes", 
          "Orthologous Steppe mouse Genes", "Orthologous Stickleback Genes", 
          "Orthologous Sumatran orangutan Genes", "Orthologous Tarsier Genes", 
          "Orthologous Tasmanian devil Genes", "Orthologous Tetraodon Genes", 
          "Orthologous Three-toed box turtle Genes", "Orthologous Tiger Genes", 
          "Orthologous Tiger tail seahorse Genes", "Orthologous Tongue sole Genes", 
          "Orthologous Tree Shrew Genes", "Orthologous Tropical clawed frog Genes", 
          "Orthologous Tuatara Genes", "Orthologous Turbot Genes", 
          "Orthologous Turkey Genes", "Orthologous Turquoise killifish Genes", 
          "Orthologous Upper Galilee mountains blind mole rat Genes", 
          "Orthologous Vaquita Genes", "Orthologous Vervet-AGM Genes", 
          "Orthologous Wallaby Genes", "Orthologous White-tufted-ear marmoset Genes", 
          "Orthologous Wild yak Genes", "Orthologous Yarkand deer Genes", 
          "Orthologous Yellowtail amberjack Genes", "Orthologous Zebra finch Genes", 
          "Orthologous Zebra mbuna Genes", "Orthologous Zebrafish Genes", 
          "Orthologous Zig-zag eel Genes", "With Interpro ID(s)", 
          "With CDD ID(s)", "With Gene3D ID(s)", "With HAMAP ID(s)", 
          "With MobiDB lite", "With Coiled-coils (Ncoils)", "With PANTHER ID(s)", 
          "With Pfam ID(s)", "With PIRSF ID(s)", "With Prints ID(s)", 
          "With PROSITE patterns ID(s)", "With PROSITE profiles ID(s)", 
          "With Low complexity (Seg)", "With SFLD ID(s)", "With PDB-ENSP mappings", 
          "With Cleavage site (Signalp)", "With SMART ID(s)", "With Superfamily ID(s)", 
          "With TIGRFAM ID(s)", "With Transmembrane helices", "Interpro ID(s) [e.g. IPR000001]", 
          "CDD ID(s) [e.g. cd00009]", "Gene3D ID(s) [e.g. 1.10.10.10]", 
          "HAMAP ID(s) [e.g. MF_00001]", "PANTHER ID(s) [e.g. PTHR10003]", 
          "Pfam ID(s) [e.g. PF00001]", "PIRSF ID(s) [e.g. PIRSF000019]", 
          "Prints ID(s) [e.g. PR00001]", "PROSITE patterns ID(s) [e.g. PS00010]", 
          "PROSITE profiles ID(s) [e.g. PS01031]", "SFLD ID(s) [e.g. SFLDF00002]", 
          "SMART ID(s) [e.g. SM00002]", "Superfamily ID(s) [e.g. SSF100879]", 
          "TIGRFAM ID(s) [e.g. TIGR00002]", "limit to genes with germline variant data sources", 
          "Variant supporting evidence", "Parent term name"), options = c("[1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,CHR_HG1_PATCH,CHR_HG26_PATCH,CHR_HG28_PATCH,CHR_HG30_PATCH,CHR_HG76_PATCH,CHR_HG107_PATCH,CHR_HG109_PATCH,CHR_HG126_PATCH,CHR_HG142_HG150_NOVEL_TEST,CHR_HG151_NOVEL_TEST,CHR_HG439_PATCH,CHR_HG545_PATCH,CHR_HG699_PATCH,CHR_HG705_PATCH,CHR_HG708_PATCH,CHR_HG721_PATCH,CHR_HG926_PATCH,CHR_HG986_PATCH,CHR_HG1277_PATCH,CHR_HG1298_PATCH,CHR_HG1309_PATCH,CHR_HG1311_PATCH,CHR_HG1320_PATCH,CHR_HG1342_HG2282_PATCH,CHR_HG1362_PATCH,CHR_HG1384_PATCH,CHR_HG1395_PATCH,CHR_HG1398_PATCH,CHR_HG1445_PATCH,CHR_HG1485_PATCH,CHR_HG1524_PATCH,CHR_HG1531_PATCH,CHR_HG1535_PATCH,CHR_HG1651_PATCH,CHR_HG1708_PATCH,CHR_HG1815_PATCH,CHR_HG1832_PATCH,CHR_HG2002_PATCH,CHR_HG2021_PATCH,CHR_HG2022_PATCH,CHR_HG2023_PATCH,CHR_HG2030_PATCH,CHR_HG2046_PATCH,CHR_HG2047_PATCH,CHR_HG2057_PATCH,CHR_HG2058_PATCH,CHR_HG2060_PATCH,CHR_HG2062_PATCH,CHR_HG2063_PATCH,CHR_HG2066_PATCH,CHR_HG2067_PATCH,CHR_HG2072_PATCH,CHR_HG2087_PATCH,CHR_HG2088_PATCH,CHR_HG2095_PATCH,CHR_HG2104_PATCH,CHR_HG2111_PATCH,CHR_HG2114_PATCH,CHR_HG2115_PATCH,CHR_HG2116_PATCH,CHR_HG2121_PATCH,CHR_HG2128_PATCH,CHR_HG2133_PATCH,CHR_HG2191_PATCH,CHR_HG2198_PATCH,CHR_HG2213_PATCH,CHR_HG2217_PATCH,CHR_HG2232_PATCH,CHR_HG2233_PATCH,CHR_HG2235_PATCH,CHR_HG2236_PATCH,CHR_HG2239_PATCH,CHR_HG2246_HG2248_HG2276_PATCH,CHR_HG2247_PATCH,CHR_HG2249_PATCH,CHR_HG2263_PATCH,CHR_HG2266_PATCH,CHR_HG2285_HG106_HG2252_PATCH,CHR_HG2288_HG2289_PATCH,CHR_HG2290_PATCH,CHR_HG2291_PATCH,CHR_HG2334_PATCH,CHR_HG2365_PATCH,CHR_HG2412_PATCH,CHR_HG2419_PATCH,CHR_HG2442_PATCH,CHR_HG2471_PATCH,CHR_HG2499_PATCH,CHR_HG2509_PATCH,CHR_HG2510_PATCH,CHR_HG2511_PATCH,CHR_HG2512_PATCH,CHR_HG2513_PATCH,CHR_HG2525_PATCH,CHR_HSCHRX_1_CTG3,CHR_HSCHRX_2_CTG3,CHR_HSCHRX_2_CTG12,CHR_HSCHR1_ALT2_1_CTG32_1,CHR_HSCHR1_1_CTG3,CHR_HSCHR1_1_CTG11,CHR_HSCHR1_1_CTG31,CHR_HSCHR1_1_CTG32_1,CHR_HSCHR1_2_CTG3,CHR_HSCHR1_2_CTG31,CHR_HSCHR1_2_CTG32_1,CHR_HSCHR1_3_CTG3,CHR_HSCHR1_3_CTG31,CHR_HSCHR1_3_CTG32_1,CHR_HSCHR1_4_CTG3,CHR_HSCHR1_4_CTG31,CHR_HSCHR1_5_CTG3,CHR_HSCHR1_5_CTG32_1,CHR_HSCHR1_6_CTG3,CHR_HSCHR1_8_CTG3,CHR_HSCHR1_9_CTG3,CHR_HSCHR2_1_CTG1,CHR_HSCHR2_1_CTG5,CHR_HSCHR2_1_CTG7,CHR_HSCHR2_1_CTG7_2,CHR_HSCHR2_1_CTG15,CHR_HSCHR2_2_CTG1,CHR_HSCHR2_2_CTG7,CHR_HSCHR2_2_CTG7_2,CHR_HSCHR2_2_CTG15,CHR_HSCHR2_3_CTG1,CHR_HSCHR2_3_CTG7_2,CHR_HSCHR2_3_CTG15,CHR_HSCHR2_4_CTG1,CHR_HSCHR2_6_CTG7_2,CHR_HSCHR2_7_CTG7_2,CHR_HSCHR2_8_CTG7_2,CHR_HSCHR3_1_CTG1,CHR_HSCHR3_1_CTG2_1,CHR_HSCHR3_1_CTG3,CHR_HSCHR3_2_CTG2_1,CHR_HSCHR3_2_CTG3,CHR_HSCHR3_3_CTG1,CHR_HSCHR3_3_CTG3,CHR_HSCHR3_4_CTG1,CHR_HSCHR3_4_CTG2_1,CHR_HSCHR3_4_CTG3,CHR_HSCHR3_5_CTG1,CHR_HSCHR3_5_CTG2_1,CHR_HSCHR3_5_CTG3,CHR_HSCHR3_6_CTG2_1,CHR_HSCHR3_6_CTG3,CHR_HSCHR3_7_CTG3,CHR_HSCHR3_8_CTG2_1,CHR_HSCHR3_8_CTG3,CHR_HSCHR3_9_CTG2_1,CHR_HSCHR3_9_CTG3,CHR_HSCHR4_1_CTG4,CHR_HSCHR4_1_CTG6,CHR_HSCHR4_1_CTG9,CHR_HSCHR4_1_CTG12,CHR_HSCHR4_2_CTG4,CHR_HSCHR4_2_CTG12,CHR_HSCHR4_3_CTG12,CHR_HSCHR4_4_CTG12,CHR_HSCHR4_5_CTG12,CHR_HSCHR4_6_CTG12,CHR_HSCHR4_7_CTG12,CHR_HSCHR4_8_CTG12,CHR_HSCHR4_9_CTG12,CHR_HSCHR4_11_CTG12,CHR_HSCHR4_12_CTG12,CHR_HSCHR5_1_CTG1,CHR_HSCHR5_1_CTG1_1,CHR_HSCHR5_1_CTG5,CHR_HSCHR5_2_CTG1,CHR_HSCHR5_2_CTG1_1,CHR_HSCHR5_2_CTG5,CHR_HSCHR5_3_CTG1,CHR_HSCHR5_3_CTG5,CHR_HSCHR5_4_CTG1,CHR_HSCHR5_4_CTG1_1,CHR_HSCHR5_5_CTG1,CHR_HSCHR5_6_CTG1,CHR_HSCHR5_7_CTG1,CHR_HSCHR5_8_CTG1,CHR_HSCHR6_MHC_APD_CTG1,CHR_HSCHR6_MHC_COX_CTG1,CHR_HSCHR6_MHC_DBB_CTG1,CHR_HSCHR6_MHC_MANN_CTG1,CHR_HSCHR6_MHC_MCF_CTG1,CHR_HSCHR6_MHC_QBL_CTG1,CHR_HSCHR6_MHC_SSTO_CTG1,CHR_HSCHR6_1_CTG2,CHR_HSCHR6_1_CTG3,CHR_HSCHR6_1_CTG4,CHR_HSCHR6_1_CTG5,CHR_HSCHR6_1_CTG6,CHR_HSCHR6_1_CTG7,CHR_HSCHR6_1_CTG8,CHR_HSCHR6_1_CTG9,CHR_HSCHR6_8_CTG1,CHR_HSCHR7_1_CTG1,CHR_HSCHR7_1_CTG4_4,CHR_HSCHR7_1_CTG6,CHR_HSCHR7_1_CTG7,CHR_HSCHR7_2_CTG1,CHR_HSCHR7_2_CTG4_4,CHR_HSCHR7_2_CTG6,CHR_HSCHR7_2_CTG7,CHR_HSCHR7_3_CTG1,CHR_HSCHR7_3_CTG4_4,CHR_HSCHR7_3_CTG6,CHR_HSCHR8_1_CTG1,CHR_HSCHR8_1_CTG6,CHR_HSCHR8_1_CTG7,CHR_HSCHR8_2_CTG1,CHR_HSCHR8_2_CTG7,CHR_HSCHR8_3_CTG1,CHR_HSCHR8_3_CTG7,CHR_HSCHR8_4_CTG1,CHR_HSCHR8_4_CTG7,CHR_HSCHR8_5_CTG1,CHR_HSCHR8_5_CTG7,CHR_HSCHR8_6_CTG1,CHR_HSCHR8_7_CTG1,CHR_HSCHR8_7_CTG7,CHR_HSCHR8_8_CTG1,CHR_HSCHR8_9_CTG1,CHR_HSCHR9_1_CTG1,CHR_HSCHR9_1_CTG2,CHR_HSCHR9_1_CTG3,CHR_HSCHR9_1_CTG4,CHR_HSCHR9_1_CTG5,CHR_HSCHR9_1_CTG6,CHR_HSCHR10_1_CTG1,CHR_HSCHR10_1_CTG2,CHR_HSCHR10_1_CTG3,CHR_HSCHR10_1_CTG4,CHR_HSCHR10_1_CTG6,CHR_HSCHR11_1_CTG1_2,CHR_HSCHR11_1_CTG3_1,CHR_HSCHR11_1_CTG5,CHR_HSCHR11_1_CTG6,CHR_HSCHR11_1_CTG7,CHR_HSCHR11_1_CTG8,CHR_HSCHR11_2_CTG1,CHR_HSCHR11_2_CTG1_1,CHR_HSCHR11_2_CTG8,CHR_HSCHR11_3_CTG1,CHR_HSCHR12_1_CTG1,CHR_HSCHR12_1_CTG2_1,CHR_HSCHR12_2_CTG2,CHR_HSCHR12_2_CTG2_1,CHR_HSCHR12_3_CTG2,CHR_HSCHR12_3_CTG2_1,CHR_HSCHR12_4_CTG2,CHR_HSCHR12_4_CTG2_1,CHR_HSCHR12_5_CTG2,CHR_HSCHR12_5_CTG2_1,CHR_HSCHR12_6_CTG2_1,CHR_HSCHR12_8_CTG2_1,CHR_HSCHR12_9_CTG2_1,CHR_HSCHR13_1_CTG1,CHR_HSCHR13_1_CTG3,CHR_HSCHR13_1_CTG5,CHR_HSCHR14_1_CTG1,CHR_HSCHR14_2_CTG1,CHR_HSCHR14_3_CTG1,CHR_HSCHR14_7_CTG1,CHR_HSCHR14_8_CTG1,CHR_HSCHR14_9_CTG1,CHR_HSCHR15_1_CTG1,CHR_HSCHR15_1_CTG3,CHR_HSCHR15_1_CTG8,CHR_HSCHR15_2_CTG3,CHR_HSCHR15_2_CTG8,CHR_HSCHR15_3_CTG3,CHR_HSCHR15_3_CTG8,CHR_HSCHR15_4_CTG8,CHR_HSCHR15_5_CTG8,CHR_HSCHR15_6_CTG8,CHR_HSCHR16_CTG2,CHR_HSCHR16_1_CTG1,CHR_HSCHR16_1_CTG3_1,CHR_HSCHR16_2_CTG3_1,CHR_HSCHR16_3_CTG1,CHR_HSCHR16_4_CTG1,CHR_HSCHR16_4_CTG3_1,CHR_HSCHR16_5_CTG1,CHR_HSCHR16_5_CTG3_1,CHR_HSCHR17_1_CTG1,CHR_HSCHR17_1_CTG2,CHR_HSCHR17_1_CTG4,CHR_HSCHR17_1_CTG5,CHR_HSCHR17_1_CTG9,CHR_HSCHR17_2_CTG1,CHR_HSCHR17_2_CTG2,CHR_HSCHR17_2_CTG4,CHR_HSCHR17_2_CTG5,CHR_HSCHR17_3_CTG1,CHR_HSCHR17_3_CTG2,CHR_HSCHR17_3_CTG4,CHR_HSCHR17_4_CTG4,CHR_HSCHR17_5_CTG4,CHR_HSCHR17_6_CTG4,CHR_HSCHR17_7_CTG4,CHR_HSCHR17_8_CTG4,CHR_HSCHR17_9_CTG4,CHR_HSCHR17_10_CTG4,CHR_HSCHR17_11_CTG4,CHR_HSCHR17_12_CTG4,CHR_HSCHR18_ALT2_CTG2_1,CHR_HSCHR18_ALT21_CTG2_1,CHR_HSCHR18_1_CTG1,CHR_HSCHR18_1_CTG1_1,CHR_HSCHR18_1_CTG2_1,CHR_HSCHR18_2_CTG1_1,CHR_HSCHR18_2_CTG2,CHR_HSCHR18_2_CTG2_1,CHR_HSCHR18_3_CTG2_1,CHR_HSCHR18_5_CTG1_1,CHR_HSCHR19_1_CTG2,CHR_HSCHR19_1_CTG3_1,CHR_HSCHR19_2_CTG2,CHR_HSCHR19_2_CTG3_1,CHR_HSCHR19_3_CTG2,CHR_HSCHR19_3_CTG3_1,CHR_HSCHR19_4_CTG2,CHR_HSCHR19_4_CTG3_1,CHR_HSCHR19_5_CTG2,CHR_HSCHR19KIR_ABC08_AB_HAP_C_P_CTG3_1,CHR_HSCHR19KIR_ABC08_AB_HAP_T_P_CTG3_1,CHR_HSCHR19KIR_ABC08_A1_HAP_CTG3_1,CHR_HSCHR19KIR_CA01-TA01_1_CTG3_1,CHR_HSCHR19KIR_CA01-TA01_2_CTG3_1,CHR_HSCHR19KIR_CA01-TB01_CTG3_1,CHR_HSCHR19KIR_CA01-TB04_CTG3_1,CHR_HSCHR19KIR_CA04_CTG3_1,CHR_HSCHR19KIR_FH05_A_HAP_CTG3_1,CHR_HSCHR19KIR_FH05_B_HAP_CTG3_1,CHR_HSCHR19KIR_FH06_A_HAP_CTG3_1,CHR_HSCHR19KIR_FH06_BA1_HAP_CTG3_1,CHR_HSCHR19KIR_FH08_A_HAP_CTG3_1,CHR_HSCHR19KIR_FH08_BAX_HAP_CTG3_1,CHR_HSCHR19KIR_FH13_A_HAP_CTG3_1,CHR_HSCHR19KIR_FH13_BA2_HAP_CTG3_1,CHR_HSCHR19KIR_FH15_A_HAP_CTG3_1,CHR_HSCHR19KIR_FH15_B_HAP_CTG3_1,CHR_HSCHR19KIR_GRC212_AB_HAP_CTG3_1,CHR_HSCHR19KIR_GRC212_BA1_HAP_CTG3_1,CHR_HSCHR19KIR_G085_A_HAP_CTG3_1,CHR_HSCHR19KIR_G085_BA1_HAP_CTG3_1,CHR_HSCHR19KIR_G248_A_HAP_CTG3_1,CHR_HSCHR19KIR_G248_BA2_HAP_CTG3_1,CHR_HSCHR19KIR_HG2393_CTG3_1,CHR_HSCHR19KIR_HG2394_CTG3_1,CHR_HSCHR19KIR_HG2396_CTG3_1,CHR_HSCHR19KIR_LUCE_A_HAP_CTG3_1,CHR_HSCHR19KIR_LUCE_BDEL_HAP_CTG3_1,CHR_HSCHR19KIR_RP5_B_HAP_CTG3_1,CHR_HSCHR19KIR_RSH_A_HAP_CTG3_1,CHR_HSCHR19KIR_RSH_BA2_HAP_CTG3_1,CHR_HSCHR19KIR_T7526_A_HAP_CTG3_1,CHR_HSCHR19KIR_T7526_BDEL_HAP_CTG3_1,CHR_HSCHR19KIR_0010-5217-AB_CTG3_1,CHR_HSCHR19KIR_0019-4656-A_CTG3_1,CHR_HSCHR19KIR_0019-4656-B_CTG3_1,CHR_HSCHR19KIR_7191059-1_CTG3_1,CHR_HSCHR19KIR_7191059-2_CTG3_1,CHR_HSCHR19KIR_502960008-1_CTG3_1,CHR_HSCHR19KIR_502960008-2_CTG3_1,CHR_HSCHR19LRC_COX1_CTG3_1,CHR_HSCHR19LRC_COX2_CTG3_1,CHR_HSCHR19LRC_LRC_I_CTG3_1,CHR_HSCHR19LRC_LRC_J_CTG3_1,CHR_HSCHR19LRC_LRC_S_CTG3_1,CHR_HSCHR19LRC_LRC_T_CTG3_1,CHR_HSCHR19LRC_PGF1_CTG3_1,CHR_HSCHR19LRC_PGF2_CTG3_1,CHR_HSCHR20_1_CTG1,CHR_HSCHR20_1_CTG2,CHR_HSCHR20_1_CTG3,CHR_HSCHR20_1_CTG4,CHR_HSCHR21_2_CTG1_1,CHR_HSCHR21_3_CTG1_1,CHR_HSCHR21_4_CTG1_1,CHR_HSCHR21_5_CTG2,CHR_HSCHR21_6_CTG1_1,CHR_HSCHR21_8_CTG1_1,CHR_HSCHR22_1_CTG1,CHR_HSCHR22_1_CTG2,CHR_HSCHR22_1_CTG3,CHR_HSCHR22_1_CTG4,CHR_HSCHR22_1_CTG5,CHR_HSCHR22_1_CTG6,CHR_HSCHR22_1_CTG7,CHR_HSCHR22_2_CTG1,CHR_HSCHR22_3_CTG1,CHR_HSCHR22_4_CTG1,CHR_HSCHR22_5_CTG1,CHR_HSCHR22_6_CTG1,CHR_HSCHR22_7_CTG1,CHR_HSCHR22_8_CTG1,GL000009.2,GL000194.1,GL000195.1,GL000205.2,GL000213.1,GL000216.2,GL000218.1,GL000219.1,GL000220.1,GL000225.1,KI270442.1,KI270711.1,KI270713.1,KI270721.1,KI270726.1,KI270727.1,KI270728.1,KI270731.1,KI270733.1,KI270734.1,KI270744.1,KI270750.1,MT,X,Y]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[IG_C_gene,IG_C_pseudogene,IG_D_gene,IG_J_gene,IG_J_pseudogene,IG_pseudogene,IG_V_gene,IG_V_pseudogene,lncRNA,miRNA,misc_RNA,Mt_rRNA,Mt_tRNA,polymorphic_pseudogene,processed_pseudogene,protein_coding,pseudogene,ribozyme,rRNA,rRNA_pseudogene,scaRNA,scRNA,snoRNA,snRNA,sRNA,TEC,transcribed_processed_pseudogene,transcribed_unitary_pseudogene,transcribed_unprocessed_pseudogene,translated_processed_pseudogene,translated_unprocessed_pseudogene,TR_C_gene,TR_D_gene,TR_J_gene,TR_J_pseudogene,TR_V_gene,TR_V_pseudogene,unitary_pseudogene,unprocessed_pseudogene,vault_RNA]", 
          "[IG_C_gene,IG_C_pseudogene,IG_D_gene,IG_J_gene,IG_J_pseudogene,IG_pseudogene,IG_V_gene,IG_V_pseudogene,lncRNA,miRNA,misc_RNA,Mt_rRNA,Mt_tRNA,nonsense_mediated_decay,non_stop_decay,polymorphic_pseudogene,processed_pseudogene,processed_transcript,protein_coding,pseudogene,retained_intron,ribozyme,rRNA,rRNA_pseudogene,scaRNA,scRNA,snoRNA,snRNA,sRNA,TEC,transcribed_processed_pseudogene,transcribed_unitary_pseudogene,transcribed_unprocessed_pseudogene,translated_processed_pseudogene,translated_unprocessed_pseudogene,TR_C_gene,TR_D_gene,TR_J_gene,TR_J_pseudogene,TR_V_gene,TR_V_pseudogene,unitary_pseudogene,unprocessed_pseudogene,vault_RNA]", 
          "[ensembl,ensembl_havana,ensembl_havana_tagene,havana,havana_tagene,insdc,mirbase]", 
          "[ensembl,ensembl_havana,ensembl_havana_tagene,ensembl_tagene,havana,havana_tagene,insdc,mirbase]", 
          "[only,excluded]", "[only,excluded]", "[only,excluded]", 
          "[only,excluded]", "[only,excluded]", "[only,excluded]", 
          "[12p12.1 microdeletion syndrome,12p12.5 intragenic deletions associated with intellectual disability,12q14 microdeletion syndrome,12q15q21.1 microdeletion syndrome,14q11.2 microduplication syndrome,15q11q13 microduplication syndrome,15q13.3 deletions phenocopy,15q13.3 microdeletion syndrome,15q14 microdeletion syndrome,15q24 microdeletion syndrome,16p13.2 microdeletion syndrome,16q24.3 microdeletion syndrome,17-Beta-Hydroxysteroid Dehydrogenase III Deficiency,17p11.2 microduplication syndrome,17p13.3 microduplication syndrome,17q11 microdeletion syndrome,17q11.2 microduplication syndrome,17q12 microdeletion syndrome,17q21.31 microdeletion syndrome,17q23.1q23.2 microdeletion syndrome,17q24.2 microdeletion syndrome,19p13.3 microduplication syndrome,1p21.3 microdeletion syndrome,1p31p32 microdeletion syndrome,1p36 deletion syndrome,1q44 microdeletion syndrome,2-aminoadipic 2-oxoadipic aciduria,2-Aminoadipic and 2-Oxoadipic Aciduria,2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency,2-methylbutyryl-CoA dehydrogenase deficiency,20p12.3  microdeletion syndrome,21q22.11q22.12 microdeletion syndrome,22q11.2 Deletion Syndrome,22q11.2 duplication syndrome,24-Dienoyl-CoA Reductase Deficiency,26708094,2p21 microdeletion syndrome,2p21 microdeletion syndrome without cystinuria,2q23.1 microdeletion syndrome,2q24 microdeletion syndrome,2q32q33 microdeletion syndrome,2q37 microdeletion syndrome,3-hydroxy-3-methylglutaric aciduria,3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY,3-HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE,3-HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE 2 DEFICIENCY,3-hydroxy-3-methylglutaryl-CoA synthase deficiency,3-HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE-2 DEFICIENCY,3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency,3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY,3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency,3-HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY,3-M syndrome 1,3-M syndrome 2,3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY,3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY,3-Methylcrotonyl-CoA Carboxylase Deficiency,3-methylglutaconic aciduria type 1,3-Methylglutaconic aciduria type 3,3-methylglutaconic aciduria type 7,3-methylglutaconic aciduria type 8,3-methylglutaconic aciduria type 9,3-METHYLGLUTACONIC ACIDURIA TYPE I,3-METHYLGLUTACONIC ACIDURIA TYPE III,3-METHYLGLUTACONIC ACIDURIA TYPE IX,3-METHYLGLUTACONIC ACIDURIA TYPE V,3-METHYLGLUTACONIC ACIDURIA TYPE VII,3-Methylglutaconic aciduria type VII with cataracts neurologic involvement and neutropenia,3-METHYLGLUTACONIC ACIDURIA TYPE VIII,3-methylglutaconic aciduria with deafness encephalopathy and Leigh-like syndrome,3-phosphoglycerate dehydrogenase deficiency infantile/juvenile form,3-phosphoserine phosphatase deficiency infantile/juvenile form,3C syndrome,3M syndrome,3MC,3MC syndrome,3MC SYNDROME 1,3MC SYNDROME 2,3MC SYNDROME 3,45X/46XY mixed gonadal dysgenesis,46XX gonadal dysgenesis,46XX ovarian dysgenesis-short stature syndrome,46XX ovotesticular disorder of sex development,46XX SEX REVERSAL 1,46XX SEX REVERSAL 4,46XX SEX REVERSAL 5,46XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS ADRENALS AND LUNGS,46XX testicular disorder of sex development,46XY complete gonadal dysgenesis,46XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency,46XY disorder of sex development due to 5-alpha-reductase 2 deficiency,46XY disorder of sex development due to isolated 17 20 lyase deficiency,46XY disorder of sex development due to testicular 1720-desmolase deficiency,46XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency,46XY GONADAL DYSGENESIS WITH MINIFASCICULAR NEUROPATHY,46XY gonadal dysgenesis-motor and sensory neuropathy syndrome,46XY partial gonadal dysgenesis,46XY SEX REVERSAL 1,46XY sex reversal 11,46XY SEX REVERSAL 2,46XY SEX REVERSAL 3,46XY SEX REVERSAL 5,46XY SEX REVERSAL 6,46XY SEX REVERSAL 7,46XY SEX REVERSAL 8,46XY sex reversal 9,5-Oxoprolinase deficiency,5p13 microduplication syndrome,5q14.3 microdeletion syndrome,5q35 microduplication syndrome,6-pyruvoyl-tetrahydropterin synthase deficiency,6-Pyruvoyltetrahydropterin Synthase Deficiency,6q terminal deletion syndrome,6q16 microdeletion syndrome,6q25 microdeletion syndrome,7q31 microdeletion syndrome,8p11.2 deletion syndrome,8p23.1 microdeletion syndrome,8Q24.3 DELETION-LIKE,8q24.3 microdeletion syndrome,9q33.3q34.11 microdeletion syndrome,AA amyloidosis,AApoAI amyloidosis,AApoAII amyloidosis,Aarskog-Scott syndrome,ABAT-related GABA-transaminase Deficiency,ABCB11-Related Intrahepatic Cholestasis,ABCD syndrome,ABDOMINAL OBESITY-METABOLIC SYNDROME 1,ABDOMINAL OBESITY-METABOLIC SYNDROME 3,ABeta amyloidosis Arctic type,ABeta amyloidosis Dutch type,ABeta amyloidosis Iowa type,ABeta amyloidosis Italian type,ABetaA21G amyloidosis,ABetaL34V amyloidosis,ABETALIPOPROTEINEMIA,Ablepharon macrostomia syndrome,Ablepharon-Macrostomia syndrome,ABNORMAL HAIR JOINT LAXITY AND DEVELOPMENTAL DELAY,ABri amyloidosis,Abruzzo-Erickson syndrome,Absence of fingerprints-congenital milia syndrome,ACATALASEMIA,Accelerated tumor formation susceptibility to,Aceruloplasminemia,ACERULOPLASMINEMIAHYPOCERULOPLASMINEMIA INCLUDED,Acetazolamide-responsive myotonia,ACETYL-CoA ACETYLTRANSFERASE-2 DEFICIENCY,ACETYL-CoA CARBOXYLASE DEFICIENCY,Acetylation slow,Achalasia-Addisonianism-Alacrima syndrome,Acheiropodia,ACHEIROPODY,Achondrogenesis type 1A,Achondrogenesis type 1B,Achondrogenesis type 2,ACHONDROGENESIS TYPE IA,ACHONDROGENESIS TYPE IB,ACHONDROGENESIS TYPE II,Achondroplasia,ACHONDROPLASIA SEVERE WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS,Achromatopsia,ACHROMATOPSIA 2,Achromatopsia 3,Achromatopsia 4,ACHROMATOPSIA 7,ACID PHOSPHATASE DEFICIENCY,Acid-labile subunit deficiency,ACNE INVERSA FAMILIAL 1,ACNE INVERSA FAMILIAL 2 WITH OR WITHOUT DOWLING-DEGOS DISEASE,ACNE INVERSA FAMILIAL 3,Acquired idiopathic sideroblastic anemia,Acquired partial lipodystrophy,Acquired schizencephaly,Acral peeling skin syndrome,Acral self-healing collodion baby,Acro-Renal-Ocular syndrome,Acrocallosal syndrome,Acrocapitofemoral dysplasia,acrocephalopolysyndactyly type 2,ACROCEPHALOSYNDACTYLY TYPE V,Acrodermatitis continua of Hallopeau,Acrodermatitis enteropathica,ACRODERMATITIS ENTEROPATHICA ZINC-DEFICIENCY TYPE,Acrodysostosis,ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE,ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE,Acrodysostosis with multiple hormone resistance,ACROFACIAL DYSOSTOSIS 1 NAGER TYPE,Acrofacial dysostosis cincinnati type,Acrofacial dysostosis Rodriguez type,Acrofacial dysostosis Weyers type,Acrogeria,Acrokeratosis verruciformis,Acrokeratosis verruciformis of Hopf,Acromegaloid facial appearance syndrome,Acromegaly,Acromelic frontonasal dysostosis,Acromelic frontonasal dysplasia,ACROMESOMELIC CHONDRODYSPLASIA GREBE TYPE,ACROMESOMELIC DYSPLASIA DEMIRHAN TYPE,Acromesomelic dysplasia Grebe type,ACROMESOMELIC DYSPLASIA HUNTER-THOMPSON TYPE,Acromesomelic dysplasia Maroteaux type,ACROMICRIC DYSPLASIA,Acroosteolysis-keloid-like lesions-premature aging syndrome,ACTB Haploinsufficiency syndtome,ACTH deficiency isolated,ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA,ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2,Action myoclonus - renal failure syndrome,Activated PI3K-delta syndrome,Actn3 deficiency,Acute basophilic leukemia,Acute encephalopathy with biphasic seizures and late reduced diffusion,Acute fatty liver of pregnancy,Acute Febrile Encephalopathy,Acute Hepatic Porphyria,Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins,Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome,Acute infantile liver failure-multisystemic involvement syndrome,Acute inflammatory demyelinating polyradiculoneuropathy,Acute intermittent porphyria,ACUTE LIVER FAILURE ALF IN INFANCY AND CHILDHOOD; SHORT STATURE OPTIC NERVE ATROPHY AND PELGER-HUET ANOMALY,Acute mast cell leukemia,Acute megakaryoblastic leukemia in Down syndrome,Acute megakaryoblastic leukemia without Down syndrome,Acute myeloblastic leukemia with maturation,Acute myeloblastic leukemia without maturation,Acute myeloid leukaemia with myelodysplasia-related features,Acute myeloid leukemia with 11q23 abnormalities,Acute myeloid leukemia with abnormal bone marrow eosinophils inv16p13q22 or t16,Acute myeloid leukemia with CEBPA somatic mutations,Acute myeloid leukemia with inv3q21q26.2 or t3,Acute myeloid leukemia with minimal differentiation,Acute myeloid leukemia with NPM1 somatic mutations,Acute myeloid leukemia with t6,Acute myeloid leukemia with t8,Acute myeloid leukemia with t9,ACUTE NECROTIZING ENCEPHALOPATHY 1 SUSCEPTIBILITY TO,Acute necrotizing encephalopathy of childhood,Acute neonatal citrullinemia type I,ACUTE PROMYELOCYTIC LEUKEMIA,Acute undifferentiated leukemia,Acyl-CoA dehydrogenase 9 deficiency,acyl-CoA dehydrogenase family member type 9 deficiency,ACYL-CoA DEHYDROGENASE MEDIUM-CHAIN DEFICIENCY OF,ACYL-CoA DEHYDROGENASE SHORT-CHAIN DEFICIENCY OF,ACYL-CoA DEHYDROGENASE VERY LONG-CHAIN DEFICIENCY OF,ACys amyloidosis,Adams Oliver syndrome,Adams-Oliver syndrome,ADAMS-OLIVER SYNDROME 1,Adams-Oliver syndrome 2,ADAMS-OLIVER SYNDROME 3,ADAMS-OLIVER SYNDROME 4,Adams-Oliver syndrome 5,ADAMS-OLIVER SYNDROME 6,ADan amyloidosis,ADARB1-associated Microcephaly Intellectual Disability and Seizures,ADCY5-related developmental disorder monoallelic,Adenine phosphoribosyltransferase deficiency,Adenocarcinoma of ovary,Adenosine Deaminase Deficiency,Adenosine monophosphate deaminase deficiency,Adenosine triphosphate elevated of erythrocytes,ADENYLATE KINASE DEFICIENCY HEMOLYTIC ANEMIA DUE TO,Adenylosuccinase deficiency,Adenylosuccinate lyase deficiency,Adenylosuccinate synthetase-like 1-related distal myopathy,Adermatoglyphia,ADIPONECTIN SERUM LEVEL OF QUANTITATIVE TRAIT LOCUS 1,ADNP syndrome,ADRENAL HYPERPLASIA CONGENITAL DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY,ADRENAL HYPERPLASIA CONGENITAL DUE TO 21-HYDROXYLASE DEFICIENCY,ADRENAL HYPERPLASIA CONGENITAL DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY,ADRENAL HYPERPLASIA CONGENITAL DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY,ADRENAL HYPOPLASIA CONGENITAL,ADRENAL INSUFFICIENCY CONGENITAL WITH 46XY SEX REVERSAL PARTIAL OR COMPLETE,Adrenocortical carcinoma,ADRENOCORTICAL CARCINOMA HEREDITARY,Adrenoleukodystrophy,ADRENOLEUKODYSTROPHY PSEUDONEONATAL,Adrenoleukodystrophy X-Linked,Adrenomyeloneuropathy,Adult hepatocellular carcinoma,Adult hypophosphatasia,Adult Krabbe disease,Adult polyglucosan body disease,Adult syndrome,Adult-onset autosomal dominant leukodystrophy,Adult-onset autosomal recessive cerebellar ataxia,Adult-onset autosomal recessive sideroblastic anemia,Adult-onset cervical dystonia DYT23 type,Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy,Adult-onset citrullinemia type I,Adult-onset distal myopathy due to VCP mutation,Adult-onset dystonia-parkinsonism,Adult-onset foveomacular vitelliform dystrophy,Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency,Adult-onset myasthenia gravis,ADVANCED SLEEP PHASE SYNDROME FAMILIAL 1,ADVANCED SLEEP PHASE SYNDROME FAMILIAL 2,ADVANCED SLEEP PHASE SYNDROME FAMILIAL 3,AFib amyloidosis,AFIBRINOGENEMIA CONGENITAL HYPOFIBRINOGENEMIA CONGENITAL INCLUDED,AGAMMAGLOBULINEMIA 2 AUTOSOMAL RECESSIVE,AGAMMAGLOBULINEMIA 3 AUTOSOMAL RECESSIVE,AGAMMAGLOBULINEMIA 4 AUTOSOMAL RECESSIVE,AGAMMAGLOBULINEMIA 5 AUTOSOMAL DOMINANT,AGAMMAGLOBULINEMIA 6 AUTOSOMAL RECESSIVE,AGAMMAGLOBULINEMIA 7 AUTOSOMAL RECESSIVE,AGAMMAGLOBULINEMIA 8 AUTOSOMAL DOMINANT,Agammaglobulinemia X-Linked,AGel amyloidosis,AGENESIS OF CORPUS CALLOSUM CARDIAC OCULAR AND GENITAL SYNDROME,AGENESIS OF THE CORPUS CALLOSUM,AGENESIS OF THE CORPUS CALLOSUM WITH MENTAL RETARDATION-OCULAR COLOBOMA-MICROGNATHIA,AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY,Aggressive systemic mastocytosis,Agnathia-holoprosencephaly-situs inversus syndrome,Agnathia-otocephaly complex,AGNATHIA-OTOCEPHALY COMPLEX biallelic,AGNATHIA-OTOCEPHALY COMPLEX monoallelic,AGO1-related developmental disorder monoallelic,AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome,AICA-ribosiduria,AICA-RIBOSURIA,AICA-RIBOSURIA DUE TO ATIC DEFICIENCY,Aicardi-Goutieres syndrome,AICARDI-GOUTIERES SYNDROME 1,Aicardi-Goutieres syndrome 1 dominant and recessive,AICARDI-GOUTIERES SYNDROME 2,AICARDI-GOUTIERES SYNDROME 3,AICARDI-GOUTIERES SYNDROME 4,AICARDI-GOUTIERES SYNDROME 5,AICARDI-GOUTIERES SYNDROME 6,Aicardi-Goutieres syndrome 7,AICARDI-GOUTIERES SYNDROME ASSOCIATED WITH A TYPE I INTERFERON SIGNATURE,AICARDI-GOUTIERES SYNDROME ASSOCIATED WITH A TYPE I INTERFERON SIGNATURE BIALLELIC,AKT2-related familial partial lipodystrophy,AL KAISSI SYNDROME,Al-Gazali syndrome,AL-GAZALI-BAKALINOVA SYNDROME,AL-RAQAD SYNDROME,Alacrima achalasia and mental retardation syndrome,Alacrimia-choreoathetosis-liver dysfunction syndrome,Alagille Syndrome,Alagille syndrome 1,Alagille syndrome 2,Alagille syndrome due to 20p12 microdeletion,Alagille syndrome due to a JAG1 point mutation,Alagille syndrome due to a NOTCH2 point mutation,ALAND ISLAND EYE DISEASE,Aland Islands eye disease,ALAZAMI SYNDROME,ALAZAMI-YUAN SYNDROME,Albers-Schonberg osteopetrosis,ALBINISM OCULAR TYPE I,ALBINISM OCULOCUTANEOUS TYPE IA,ALBINISM OCULOCUTANEOUS TYPE IB,ALBINISM OCULOCUTANEOUS TYPE II,ALBINISM OCULOCUTANEOUS TYPE III,ALBINISM OCULOCUTANEOUS TYPE IV,Albinism oculocutaneous type VI,ALBINISM OCULOCUTANEOUS TYPE VII,ALBRIGHT HEREDITARY OSTEODYSTROPHY,Alcohol dependence,ALCOHOL SENSITIVITY ACUTE HANGOVER SUSCEPTIBILITY TO INCLUDED,ALDEHYDE DEHYDROGENASE 2 FAMILY,ALDH18A1-related De Barsy syndrome,Alexander disease,Alexander disease type I,Alexander disease type II,ALG1-CDG,ALG11-CDG,ALG12-CDG,ALG13-CDG,ALG2-CDG,ALG3-CDG,ALG6-CDG,ALG8-CDG,ALG9-CDG,ALK-positive anaplastic large cell lymphoma,ALK-positive large B-cell lymphoma,Alkaline ceramidase 3 deficiency,Alkaptonuria,ALKURAYA-KUCINSKAS SYNDROME,ALLAN-HERNDON-DUDLEY SYNDROME,ALLANTOICASE,Allergic rhinitis,Alobar holoprosencephaly,Alopecia and T-Cell Immunodeficiency,ALOPECIA NEUROLOGIC DEFECTS AND ENDOCRINOPATHY SYNDROME,Alopecia universalis,ALOPECIA UNIVERSALIS CONGENITA,Alopecia-intellectual disability syndrome,ALOPECIA-MENTAL RETARDATION SYNDROME 1,ALOPECIA-MENTAL RETARDATION SYNDROME 4,Alpers-Huttenlocher syndrome,Alpha delta granule deficiency,ALPHA-1-ANTITRYPSIN DEFICIENCY,ALPHA-2-PLASMIN INHIBITOR DEFICIENCY,ALPHA-2C-ADRENERGIC RECEPTOR,Alpha-B crystallin-related late-onset myopathy,Alpha-dystroglycan-related  limb-girdle muscular dystrophy R16,ALPHA-FETOPROTEIN DEFICIENCY,Alpha-fetoprotein hereditary persistence of,ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY,Alpha-mannosidosis adult form,Alpha-mannosidosis infantile form,ALPHA-METHYLACETOACETIC ACIDURIA,ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY,Alpha-N-acetylgalactosaminidase deficiency type 1,Alpha-N-acetylgalactosaminidase deficiency type 2,Alpha-N-acetylgalactosaminidase deficiency type 3,Alpha-sarcoglycan-related  limb-girdle muscular dystrophy R3,ALPHA-THALASSEMIA,Alpha-thalassemia - intellectual disability syndrome linked to chromosome 16,Alpha-thalassemia - myelodysplastic syndrome,ALPHA-THALASSEMIA MENTAL RETARDATION SYNDROME X-LINKED NON-DELETION TYPE,ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME,Alpha-thalassemia-X-linked intellectual disability syndrome,ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME X-LINKED,ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION SEVERE CYTOMEGALOVIRUS INFECTION AND AUTOIMMUNITY,ALPORT SYNDROME 1 X-LINKED,ALPORT SYNDROME 2 AUTOSOMAL RECESSIVE,Alport syndrome 3 autosomal dominant,Alport syndrome autosomal dominant,ALPORT SYNDROME AUTOSOMAL RECESSIVE,Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome,Als2-Related disorders,Alstrom syndrome,ALTERNATING HEMIPLEGIA OF CHILDHOOD,Alternating hemiplegia of childhood 1,ALTERNATING HEMIPLEGIA OF CHILDHOOD 2,Alveolar capillary dysplasia with misalignment of pulmonary veins,Alveolar rhabdomyosarcoma,ALVEOLAR SOFT PART SARCOMA,Alveolar soft-tissue sarcoma,ALys amyloidosis,Alzheimer disease,ALZHEIMER DISEASE 18,Alzheimer disease 2,Alzheimer disease 3,ALZHEIMER DISEASE 4,ALZHEIMER DISEASE 9 SUSCEPTIBILITY TO,AMED SYNDROME DIGENIC,AMEGAKARYOCYTIC THROMBOCYTOPENIA CONGENITAL,AMELIA POSTERIOR WITH PELVIC AND PULMONARY HYPOPLASIA SYNDROME,Amelocerebrohypohidrotic syndrome,Amelogenesis imperfecta and gingival fibromatosis syndrome,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA1,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA2,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA3,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA4,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA5,AMELOGENESIS IMPERFECTA HYPOMATURATION TYPE IIA6,Amelogenesis imperfecta type IA,AMELOGENESIS IMPERFECTA TYPE IB,AMELOGENESIS IMPERFECTA TYPE IC,AMELOGENESIS IMPERFECTA TYPE IE,AMELOGENESIS IMPERFECTA TYPE IF,AMELOGENESIS IMPERFECTA TYPE IG,AMELOGENESIS IMPERFECTA TYPE IH,AMELOGENESIS IMPERFECTA TYPE IIIA,AMELOGENESIS IMPERFECTA TYPE IIIB,AMELOGENESIS IMPERFECTA TYPE IIIC,AMELOGENESIS IMPERFECTA TYPE IJ,AMELOGENESIS IMPERFECTA TYPE IV,AMELOGENESIS IMPERFECTA.,Aminoacylase 1 deficiency,Aminoacylase-1 deficiency,AMISH INFANTILE EPILEPSY SYNDROME,Amish lethal microcephaly,Amish nemaline myopathy,Amyelogenesis,Amyloidosis cutis dyschromia,AMYLOIDOSIS FAMILIAL VISCERAL,AMYLOIDOSIS FINNISH TYPE,AMYLOIDOSIS HEREDITARY TRANSTHYRETIN-RELATED,AMYLOIDOSIS PRIMARY LOCALIZED CUTANEOUS 1,AMYLOIDOSIS PRIMARY LOCALIZED CUTANEOUS 2,AMYLOIDOSIS PRIMARY LOCALIZED CUTANEOUS 3,Amyotrophic lateral sclerosis,AMYOTROPHIC LATERAL SCLEROSIS 1,AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,AMYOTROPHIC LATERAL SCLEROSIS 11,AMYOTROPHIC LATERAL SCLEROSIS 12 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,AMYOTROPHIC LATERAL SCLEROSIS 16 JUVENILE,AMYOTROPHIC LATERAL SCLEROSIS 18,Amyotrophic lateral sclerosis 19,AMYOTROPHIC LATERAL SCLEROSIS 2 JUVENILE,Amyotrophic lateral sclerosis 20,AMYOTROPHIC LATERAL SCLEROSIS 21,Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia,AMYOTROPHIC LATERAL SCLEROSIS 23,AMYOTROPHIC LATERAL SCLEROSIS 26 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,AMYOTROPHIC LATERAL SCLEROSIS 4 JUVENILE,AMYOTROPHIC LATERAL SCLEROSIS 5 JUVENILE,AMYOTROPHIC LATERAL SCLEROSIS 6 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,AMYOTROPHIC LATERAL SCLEROSIS 8,AMYOTROPHIC LATERAL SCLEROSIS 9,AMYOTROPHIC LATERAL SCLEROSIS SUSCEPTIBILITY TO 24,AMYOTROPHIC LATERAL SCLEROSIS SUSCEPTIBILITY TO 25,Amyotrophic lateral sclerosis type 4,AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1,AMYOTROPHY HEREDITARY NEURALGIC,Analbuminemia,Anaplastic astrocytoma,Anaplastic oligoastrocytoma,Anaplastic oligodendroglioma,Anauxetic dysplasia,ANAUXETIC DYSPLASIA 1,ANAUXETIC DYSPLASIA 2,ANAUXETIC DYSPLASIA 3,ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS,Andersen-Tawil Syndrome,ANDROGEN INSENSITIVITY PARTIAL,ANDROGEN INSENSITIVITY SYNDROME,ANE syndrome,ANEMIA CONGENITAL DYSERYTHROPOIETIC TYPE Ib,ANEMIA CONGENITAL DYSERYTHROPOIETIC TYPE II,ANEMIA CONGENITAL DYSERYTHROPOIETIC TYPE IV,ANEMIA DYSERYTHROPOIETIC CONGENITAL TYPE II,ANEMIA DYSERYTHROPOIETIC CONGENITAL TYPE IV,ANEMIA HYPOCHROMIC MICROCYTIC WITH IRON OVERLOAD 1,ANEMIA HYPOCHROMIC MICROCYTIC WITH IRON OVERLOAD 2,Anemia nonspherocytic hemolytic due to g6pd deficiency,ANEMIA SIDEROBLASTIC 1,ANEMIA SIDEROBLASTIC 2 PYRIDOXINE-REFRACTORY,ANEMIA SIDEROBLASTIC 3 PYRIDOXINE-REFRACTORY,ANEMIA SIDEROBLASTIC 4,Anemia sideroblastic and spinocerebellar ataxia,ANEMIA SIDEROBLASTIC PYRIDOXINE-REFRACTORY AUTOSOMAL RECESSIVE,Anemia sideroblastic with ataxia,ANEMIA X-LINKED WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES,Anencephaly,ANEURYSM INTRACRANIAL BERRY 12,Aneurysm-osteoarthritis syndrome,Angel-shaped phalango-epiphyseal dysplasia,Angelman syndrome,Angelman syndrome due to a point mutation,Angelman syndrome due to imprinting defect in 15q11-q13,Angelman syndrome due to maternal 15q11q13 deletion,Angelman syndrome due to paternal uniparental disomy of chromosome 15,Angiocentric glioma,ANGIOEDEMA HEREDITARY TYPE I,ANGIOEDEMA HEREDITARY TYPE III,ANGIOEDEMA INDUCED BY ACE INHIBITORS SUSCEPTIBILITY TO,Angiopathy hereditary with nephropathy aneurysms and muscle cramps,ANGIOTENSIN I-CONVERTING ENZYME,ANGIOTENSINOGEN,ANGPT1-related hereditary angioedema with normal C1Inh,Anhaptoglobinemia,ANHIDROSIS ISOLATED WITH NORMAL SWEAT GLANDS,Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome,Aniridia,ANIRIDIA 1,ANIRIDIA 2,ANIRIDIA 3,Aniridia-cerebellar ataxia-intellectual disability syndrome,ANK2-related neurodevelopmental disorder,ANK3-related intellectual disability-sleep disturbance syndrome,ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE,Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome,Annular epidermolytic ichthyosis,ANO1-associated intestinal disease,Anoctamin-5-related  limb-girdle muscular dystrophy R12,Anonychia congenita,Anonychia congenita totalis,Anophthalmia/Microphthalmia,Anophthalmia/microphthalmia-esophageal atresia syndrome,ANOREXIA NERVOSA SUSCEPTIBILITY TO,Antenatal Bartter syndrome,Anterior maxillary protrusion-strabismus-intellectual disability syndrome,Anterior segment developmental anomaly,Anterior Segment Dysgenesis,ANTERIOR SEGMENT DYSGENESIS 1,ANTERIOR SEGMENT DYSGENESIS 2,ANTERIOR SEGMENT DYSGENESIS 3,ANTERIOR SEGMENT DYSGENESIS 4,ANTERIOR SEGMENT DYSGENESIS 5,ANTERIOR SEGMENT DYSGENESIS 6,ANTERIOR SEGMENT DYSGENESIS 7,ANTERIOR SEGMENT DYSGENESIS 8,ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS,Antithrombin III deficiency,Antley-Bixler syndrome,Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis,Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis,ANXIETYHARM AVOIDANCE INCLUDED,AORTIC ANEURYSM FAMILIAL THORACIC 10,AORTIC ANEURYSM FAMILIAL THORACIC 11 SUSCEPTIBILITY TO,Aortic aneurysm familial thoracic 4,AORTIC ANEURYSM FAMILIAL THORACIC 6,AORTIC ANEURYSM FAMILIAL THORACIC 7,Aortic aneurysm familial thoracic 8,Aortic aneurysm familial thoracic 9,AORTIC VALVE DISEASE 1,AORTIC VALVE DISEASE 2,AORTIC VALVE DISEASE 3,AP2S1-related developmental disorder monoallelic,APC-related attenuated familial adenomatous polyposis,APERT SYNDROME,Aplasia cutis congenita,APLASIA CUTIS CONGENITA NONSYNDROMIC,APLASIA OF LACRIMAL AND SALIVARY GLANDS,APLASTIC ANEMIA APLASTIC ANEMIA SUSCEPTIBILITY TO INCLUDED,APOCRINE GLAND SECRETION VARIATION IN,APOLIPOPROTEIN A-I DEFICIENCY,APOLIPOPROTEIN A-II,APOLIPOPROTEIN C-II DEFICIENCY,APOLIPOPROTEIN C-III DEFICIENCY,APPARENT MINERALOCORTICOID EXCESS,Aquagenic palmoplantar keratoderma,ARBOLEDA-THAM SYNDROME,ARF1-related developmental disorder monoallelic,ARGININE:GLYCINE AMIDINOTRANSFERASE DEFICIENCY,Argininemia,Argininosuccinate Lyase Deficiency,ARGININOSUCCINIC ACIDURIA,ARHGAP35-related developmental disorder monoallelic,ARHGEF9-related developmental disorder X-linked dominant,ARID2-Coffin-Siris like disorder,Arnold-Chiari malformation type I,Arnold-Chiari malformation type II,ARNT2-associated hypopituitarism post-natal microcephaly visual and renal anomalies,AROMATASE DEFICIENCY,AROMATASE EXCESS SYNDROME,AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 1,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 10,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 11,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 12,Arrhythmogenic right ventricular dysplasia familial 13,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 14,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 2,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 5,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 8,ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 9,ARTERIAL CALCIFICATION GENERALIZED OF INFANCY 1,Arterial calcification generalized of infancy 2,ARTERIAL TORTUOSITY SYNDROME,ARTERIOVENOUS MALFORMATIONS OF THE BRAIN,Arthrochalasia Ehlers-Danlos syndrome,ARTHROGRYPOSIS CLEFT PALATE CRANIOSYNOSTOSIS AND IMPAIRED INTELLECTUAL DEVELOPMENT,ARTHROGRYPOSIS DISTAL TYPE 1,ARTHROGRYPOSIS DISTAL TYPE 1A,ARTHROGRYPOSIS DISTAL TYPE 1B,ARTHROGRYPOSIS DISTAL TYPE 1C,ARTHROGRYPOSIS DISTAL TYPE 2A,ARTHROGRYPOSIS DISTAL TYPE 2B1,ARTHROGRYPOSIS DISTAL TYPE 2B2,ARTHROGRYPOSIS DISTAL TYPE 2B3,Arthrogryposis distal type 3,ARTHROGRYPOSIS DISTAL TYPE 5,ARTHROGRYPOSIS DISTAL TYPE 5D,ARTHROGRYPOSIS DISTAL TYPE 7,ARTHROGRYPOSIS DISTAL WITH IMPAIRED PROPRIOCEPTION AND TOUCH,Arthrogryposis lethal with anterior horn cell disease,ARTHROGRYPOSIS MENTAL RETARDATION AND SEIZURES,Arthrogryposis multiplex congenita,ARTHROGRYPOSIS MULTIPLEX CONGENITA 1 NEUROGENIC WITH MYELIN DEFECT,ARTHROGRYPOSIS MULTIPLEX CONGENITA 2 NEUROGENIC TYPE,ARTHROGRYPOSIS MULTIPLEX CONGENITA 3 MYOGENIC TYPE,ARTHROGRYPOSIS MULTIPLEX CONGENITA 4 NEUROGENIC WITH AGENESIS OF THE CORPUS CALLOSUM,ARTHROGRYPOSIS MULTIPLEX CONGENITA 5,Arthrogryposis Multiplex Congenita and Intellectual Disability,ARTHROGRYPOSIS MULTIPLEX CONGENITA AND INTELLECTUAL DISABILITY hemizygous,ARTHROGRYPOSIS PERTHES DISEASE AND UPWARD GAZE PALSY,ARTHROGRYPOSIS RENAL DYSFUNCTION AND CHOLESTASIS 1,Arthrogryposis renal dysfunction and cholestasis 2,Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome,Arthrogryposis-anterior horn cell disease syndrome,Arthrogryposis-renal dysfunction-cholestasis syndrome,Arts syndrome,Arylsulfatase A Deficiency,Asparagine synthetase deficiency,ASPARTATE AMINOTRANSFERASE SERUM LEVEL OF QUANTITATIVE TRAIT LOCUS 1,ASPARTYLGLUCOSAMINURIA,ASPERGER,ASPERGER SYNDROME X-LINKED SUSCEPTIBILITY TO 1,ASPERGER SYNDROME X-LINKED SUSCEPTIBILITY TO 2,Aspergillosis susceptibility to,ASPHYXIATING THORACIC DYSTROPHY 2,Asphyxiating thoracic dystrophy 5,ASPLENIA ISOLATED CONGENITAL,ASTHMA NASAL POLYPS AND ASPIRIN INTOLERANCE,ASTHMA SUSCEPTIBILITY TO,ASTHMA-RELATED TRAITS SUSCEPTIBILITY TO 1,ASTHMA-RELATED TRAITS SUSCEPTIBILITY TO 2,ASTHMA-RELATED TRAITS SUSCEPTIBILITY TO 5,ASTHMA-RELATED TRAITS SUSCEPTIBILITY TO 7,ATAD3A disorder -  global developmental delay hypotonia optic atrophy axonal neuropathy and hypertrophic cardiomyopathy,Ataxia combined cerebellar and peripheral with hearing loss and diabetes mellitus,Ataxia dysmetria contractures and scoliosis with normal cognition but loss of discriminative touch perception,ATAXIA EARLY-ONSET WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA,Ataxia posterior column with retinitis pigmentosa,ATAXIA SENSORY 1 AUTOSOMAL DOMINANT,Ataxia spastic 5 autosomal recessive,ATAXIA TELANGIECTASIA-LIKE DISORDER,Ataxia with Oculomotor Apraxia 1,ATAXIA WITH VITAMIN 3 DEFICIENCY,Ataxia with vitamin E deficiency,Ataxia-hypogonadism-choroidal dystrophy syndrome,Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome,Ataxia-oculomotor apraxia 3,ATAXIA-OCULOMOTOR APRAXIA 4,Ataxia-oculomotor apraxia type 1,Ataxia-oculomotor apraxia type 4,Ataxia-Pancytopenia Syndrome,ATAXIA-TELANGIECTASIA,ATAXIA-TELANGIECTASIA VARIANT,Ataxia-telangiectasia-like disorder,ATAXIA-TELANGIECTASIA-LIKE DISORDER 1,Ataxia-telangiectasia-like disorder 2,Atelosteogenesis type 1,Atelosteogenesis type 3,Atelosteogenesis type I,Atelosteogenesis type II,Atelosteogenesis type III,Athabaskan brainstem dysgenesis syndrome,ATHELIA,Athyreosis,ATP13A2-related juvenile neuronal ceroid lipofuscinosis,ATP5F1D metabolic disorder,ATP6V0A1-related developmental disorder monoallelic,ATP6V0C-related Developmental Disorder,ATP8B1-Related Intrahepatic Cholestasis,Atransferrinemia,ATRIAL FIBRILLATION FAMILIAL 10,ATRIAL FIBRILLATION FAMILIAL 11,ATRIAL FIBRILLATION FAMILIAL 12,Atrial fibrillation familial 13,Atrial fibrillation familial 14,Atrial fibrillation familial 15,ATRIAL FIBRILLATION FAMILIAL 18,ATRIAL FIBRILLATION FAMILIAL 3,ATRIAL FIBRILLATION FAMILIAL 4,ATRIAL FIBRILLATION FAMILIAL 6,ATRIAL FIBRILLATION FAMILIAL 7,ATRIAL FIBRILLATION FAMILIAL 9,ATRIAL SEPTAL DEFECT 2,ATRIAL SEPTAL DEFECT 3,ATRIAL SEPTAL DEFECT 4,ATRIAL SEPTAL DEFECT 5,ATRIAL SEPTAL DEFECT 6,Atrial septal defect 7 with or without atrioventricular conduction defects,ATRIAL SEPTAL DEFECT 8,Atrial septal defect 9,Atrial septal defect ostium primum type,Atrial septal defect ostium secundum type,Atrial septal defect sinus venosus type,ATRIAL SEPTAL DEFECT TYPE 2,ATRIAL SEPTAL DEFECT TYPE 3,ATRIAL SEPTAL DEFECT TYPE 4,ATRIAL SEPTAL DEFECT TYPE 6,ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS,Atrial septal defect-atrioventricular conduction defects syndrome,Atrial standstill,ATRIAL STANDSTILL 1,ATRIAL STANDSTILL 2,ATRICHIA WITH PAPULAR LESIONS,ATRIOVENTRICULAR SEPTAL DEFECT 3,ATRIOVENTRICULAR SEPTAL DEFECT 4,Atrioventricular septal defect 5,ATRIOVENTRICULAR SEPTAL DEFECT SUSCEPTIBILITY TO 2,Atrophoderma vermiculata,ATTENTION DEFICIT-HYPERACTIVITY DISORDER,ATTENTION DEFICIT-HYPERACTIVITY DISORDER SUSCEPTIBILITY TO 7,Attenuated Chediak-Higashi syndrome,ATTRV122I amyloidosis,ATTRV30M amyloidosis,Atypical chronic myeloid leukemia,Atypical dentin dysplasia due to SMOC2 deficiency,Atypical dominant Fanconi syndrome with MODY,Atypical Gaucher disease due to saposin C deficiency,Atypical glycine encephalopathy,Atypical hemolytic uremic syndrome with complement gene abnormality,Atypical hemolytic-uremic syndrome with anti-factor H antibodies,Atypical hypotonia - cystinuria syndrome,Atypical juvenile parkinsonism,atypical Krabbe disease,Atypical Noonan syndrome,Atypical pantothenate kinase associated neurodegeneration,Atypical Rett syndrome,Atypical teratoid rhabdoid tumor,Atypical Werner syndrome,Au-Kline syndrome,AUDITORY NEUROPATHY AND OPTIC ATROPHY,Auditory neuropathy autosomal dominant 1,Auditory neuropathy-optic atrophy syndrome,Aural atresia congenital,Auriculocondylar syndrome,AURICULOCONDYLAR SYNDROME 1,AURICULOCONDYLAR SYNDROME 2,Auriculocondylar syndrome 3,Autism,Autism and Syndromic Intellectual Disability,Autism intellectual disability basal ganglia dysfunction and epilepsy,AUTISM OR INTELLECTUAL DISABILITY,Autism spectrum disorder due to AUTS2 deficiency,Autism spectrum disorder-epilepsy-arthrogryposis syndrome,Autism Spectrum Disorders,AUTISM SUSCEPTIBILITY TO 15,AUTISM SUSCEPTIBILITY TO 16,AUTISM SUSCEPTIBILITY TO 17,AUTISM SUSCEPTIBILITY TO 18,AUTISM SUSCEPTIBILITY TO 19,AUTISM SUSCEPTIBILITY TO 20,AUTISM SUSCEPTIBILITY TO X-LINKED 1,AUTISM SUSCEPTIBILITY TO X-LINKED 2,AUTISM SUSCEPTIBILITY TO X-LINKED 3,AUTISM SUSCEPTIBILITY TO X-LINKED 4,AUTISM SUSCEPTIBILITY TO X-LINKED 5,AUTISM SUSCEPTIBILITY TO X-LINKED 6,Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency,Autism/ID,AUTOIMMUNE DISEASE MULTISYSTEM INFANTILE-ONSET 1,AUTOIMMUNE DISEASE MULTISYSTEM INFANTILE-ONSET 2,AUTOIMMUNE DISEASE MULTISYSTEM WITH FACIAL DYSMORPHISM,AUTOIMMUNE DISEASE SUSCEPTIBILITY TO 1,AUTOIMMUNE DISEASE SUSCEPTIBILITY TO 6,AUTOIMMUNE DISEASE SYNDROMIC MULTISYSTEM,Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome,Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome,Autoimmune interstitial lung disease-arthritis syndrome,AUTOIMMUNE INTERSTITIAL LUNG JOINT AND KIDNEY DISEASE,Autoimmune lymphoproliferative syndrome,Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency,AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME TYPE IIA,AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME TYPE III,AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME TYPE V,Autoimmune lymphoproliferative syndrome with recurrent viral infections,AUTOIMMUNE POLYENDOCRINE SYNDROME TYPE I WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA,Autoimmune Polyendocrinopathy Syndrome Type 1,Autoimmune polyendocrinopathy type 1,AUTOIMMUNE THYROID DISEASE SUSCEPTIBILITY TO 3,AUTOINFLAMMATION ANTIBODY DEFICIENCY AND IMMUNE DYSREGULATION,Autoinflammation antibody deficiency and immune dysregulation plcg2-associated,AUTOINFLAMMATION IMMUNE DYSREGULATION AND EOSINOPHILIA,Autoinflammation panniculitis and dermatosis syndrome,AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS,AUTOINFLAMMATION WITH EPISODIC FEVER AND LYMPHADENOPATHY,Autoinflammation with infantile enterocolitis,Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation,Autoinflammatory syndrome familial Behcet-like,Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis,Autosomal agammaglobulinemia,Autosomal dominant adult-onset proximal spinal muscular atrophy,Autosomal dominant Alport syndrome,Autosomal dominant aplasia and myelodysplasia,Autosomal dominant brachyolmia,Autosomal dominant centronuclear myopathy,Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons,Autosomal dominant Charcot-Marie-Tooth disease type 2A1,Autosomal dominant Charcot-Marie-Tooth disease type 2A2,Autosomal dominant Charcot-Marie-Tooth disease type 2B,Autosomal dominant Charcot-Marie-Tooth disease type 2C,Autosomal dominant Charcot-Marie-Tooth disease type 2D,Autosomal dominant Charcot-Marie-Tooth disease type 2DD,Autosomal dominant Charcot-Marie-Tooth disease type 2E,Autosomal dominant Charcot-Marie-Tooth disease type 2F,Autosomal dominant Charcot-Marie-Tooth disease type 2I,Autosomal dominant Charcot-Marie-Tooth disease type 2J,Autosomal dominant Charcot-Marie-Tooth disease type 2K,Autosomal dominant Charcot-Marie-Tooth disease type 2L,Autosomal dominant Charcot-Marie-Tooth disease type 2M,Autosomal dominant Charcot-Marie-Tooth disease type 2N,Autosomal dominant Charcot-Marie-Tooth disease type 2O,Autosomal dominant Charcot-Marie-Tooth disease type 2Q,Autosomal dominant Charcot-Marie-Tooth disease type 2U,Autosomal dominant Charcot-Marie-Tooth disease type 2V,Autosomal dominant Charcot-Marie-Tooth disease type 2W,Autosomal dominant Charcot-Marie-Tooth disease type 2Y,Autosomal dominant Charcot-Marie-Tooth disease type 2Z,Autosomal Dominant Coloboma,Autosomal dominant congenital benign spinal muscular atrophy,Autosomal dominant cutis laxa,Autosomal dominant deafness-onychodystrophy syndrome,Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome,Autosomal dominant distal renal tubular acidosis,Autosomal dominant dopa-responsive dystonia,Autosomal dominant Emery-Dreifuss muscular dystrophy,Autosomal dominant epidermolytic ichthyosis,Autosomal dominant epilepsy with auditory features,Autosomal dominant focal dystonia DYT25 type,Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering,Autosomal dominant generalized dystrophic epidermolysis bullosa,Autosomal dominant generalized epidermolysis bullosa simplex intermediate form,Autosomal dominant generalized epidermolysis bullosa simplex severe form,Autosomal dominant hyper IgE syndrome,Autosomal dominant hyperinsulinism due to Kir6.2 deficiency,Autosomal dominant hyperinsulinism due to SUR1 deficiency,Autosomal dominant hypocalcemia,Autosomal dominant hypohidrotic ectodermal dysplasia,Autosomal dominant hypophosphatemic rickets,Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome,Autosomal dominant intermediate Charcot-Marie-Tooth disease type B,Autosomal dominant intermediate Charcot-Marie-Tooth disease type C,Autosomal dominant intermediate Charcot-Marie-Tooth disease type D,Autosomal dominant intermediate Charcot-Marie-Tooth disease type E,Autosomal dominant intermediate Charcot-Marie-Tooth disease type F,Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain,Autosomal dominant Kenny-Caffey syndrome,Autosomal dominant keratitis,Autosomal dominant Larsen syndrome,Autosomal dominant limb-girdle muscular dystrophy type 1A,Autosomal dominant macrothrombocytopenia,Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,Autosomal dominant mitochondrial myopathy with exercise intolerance,Autosomal dominant multiple pterygium syndrome,Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome,Autosomal dominant neovascular inflammatory vitreoretinopathy,Autosomal dominant nocturnal frontal lobe epilepsy,Autosomal dominant non-syndromic intellectual disability,Autosomal dominant non-syndromic sensorineural deafness type DFNA,Autosomal dominant oculodentodigital dysplasia,Autosomal dominant omodysplasia,Autosomal dominant optic atrophy and cataract,Autosomal dominant optic atrophy classic form,Autosomal dominant optic atrophy plus syndrome,Autosomal dominant osteopetrosis type 1,Autosomal dominant otospondylomegaepiphyseal dysplasia,Autosomal dominant palmoplantar keratoderma and congenital alopecia,AUTOSOMAL DOMINANT PARTIAL EPILEPSY WITH AUDITORY FEATURES,Autosomal dominant polycystic kidney disease,Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis,Autosomal dominant popliteal pterygium syndrome,Autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome,Autosomal dominant primary hypomagnesemia with hypocalciuria,Autosomal dominant primary microcephaly,Autosomal dominant progressive external ophthalmoplegia,Autosomal dominant rhegmatogenous retinal detachment,Autosomal dominant Robinow syndrome,Autosomal dominant secondary polycythemia,Autosomal dominant severe congenital neutropenia,Autosomal dominant slowed nerve conduction velocity,Autosomal dominant spastic ataxia type 1,Autosomal dominant spastic paraplegia type 10,Autosomal dominant spastic paraplegia type 12,Autosomal dominant spastic paraplegia type 13,Autosomal dominant spastic paraplegia type 17,Autosomal dominant spastic paraplegia type 3,Autosomal dominant spastic paraplegia type 31,Autosomal dominant spastic paraplegia type 4,Autosomal dominant spastic paraplegia type 42,Autosomal dominant spastic paraplegia type 6,Autosomal dominant spastic paraplegia type 73,Autosomal dominant spastic paraplegia type 8,Autosomal dominant spastic paraplegia type 9A,Autosomal dominant spastic paraplegia type 9B,Autosomal dominant spondylocostal dysostosis,Autosomal dominant striatal neurodegeneration,Autosomal dominant thrombocytopenia with platelet secretion defect,Autosomal dominant vitreoretinochoroidopathy,Autosomal erythropoietic protoporphyria,Autosomal recessive Alport syndrome,Autosomal recessive anterior segment dysgenesis,Autosomal recessive ataxia Beauce type,Autosomal recessive ataxia due to PEX10 deficiency,Autosomal recessive ataxia due to ubiquinone deficiency,Autosomal recessive axonal neuropathy with neuromyotonia,Autosomal recessive bestrophinopathy,Autosomal recessive brachyolmia,Autosomal recessive centronuclear myopathy,Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency,Autosomal recessive cerebellar ataxia due to STUB1 deficiency,Autosomal recessive cerebellar ataxia with late-onset spasticity,Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency,Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency,Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency,Autosomal recessive cerebellar ataxia-psychomotor delay syndrome,Autosomal recessive cerebelloparenchymal disorder type 3,Autosomal recessive cerebral atrophy,Autosomal recessive Charcot Marie Tooth disease type 2X,Autosomal recessive Charcot-Marie-Tooth disease with hoarseness,Autosomal recessive chorioretinopathy-microcephaly syndrome,Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction,Autosomal Recessive Complicated Spastic Paraparesis SPG23,Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency,Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency,Autosomal Recessive Craniosynostosis,Autosomal Recessive Cutis Laxa,Autosomal recessive cutis laxa type 1,Autosomal recessive cutis laxa type 2 classic type,Autosomal recessive cutis laxa type 2B,Autosomal recessive distal renal tubular acidosis,Autosomal recessive dopa-responsive dystonia,Autosomal recessive Emery-Dreifuss muscular dystrophy,Autosomal recessive epidermolytic ichthyosis,Autosomal recessive extra-oral halitosis,Autosomal recessive generalized dystrophic epidermolysis bullosa intermediate form,Autosomal recessive generalized dystrophic epidermolysis bullosa severe form,Autosomal recessive generalized epidermolysis bullosa simplex,Autosomal recessive hyperinsulinism due to Kir6.2 deficiency,Autosomal recessive hyperinsulinism due to SUR1 deficiency,Autosomal recessive hypohidrotic ectodermal dysplasia,Autosomal recessive hypophosphatemic rickets,Autosomal recessive infantile hypercalcemia,Autosomal recessive intermediate Charcot-Marie-Tooth disease type A,Autosomal recessive intermediate Charcot-Marie-Tooth disease type B,Autosomal recessive intermediate Charcot-Marie-Tooth disease type C,Autosomal recessive intermediate Charcot-Marie-Tooth disease type D,Autosomal recessive isolated optic atrophy,Autosomal recessive lower motor neuron disease with childhood onset,Autosomal recessive malignant osteopetrosis,Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency,Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial JAK1 deficiency,Autosomal Recessive Mental Retardation,Autosomal recessive multiple pterygium syndrome,Autosomal recessive myogenic arthrogryposis multiplex congenita,Autosomal recessive nail dysplasia,Autosomal recessive non-syndromic intellectual disability,Autosomal recessive non-syndromic sensorineural deafness type DFNB,AUTOSOMAL RECESSIVE OCULODENTODIGITAL DYSPLASIA,Autosomal recessive omodysplasia,Autosomal recessive optic atrophy OPA7 type,AUTOSOMAL RECESSIVE OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA,Autosomal recessive polycystic kidney disease,Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity,Autosomal recessive primary microcephaly,Autosomal recessive progressive external ophthalmoplegia,Autosomal recessive proximal renal tubular acidosis,Autosomal recessive Robinow syndrome,Autosomal recessive severe congenital neutropenia due to CSF3R deficiency,Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency,Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency,Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency,Autosomal recessive sideroblastic anemia,Autosomal recessive spastic ataxia of Charlevoix-Saguenay,Autosomal recessive spastic ataxia with leukoencephalopathy,Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome,Autosomal recessive spastic paraplegia type 11,Autosomal recessive spastic paraplegia type 15,Autosomal recessive spastic paraplegia type 18,Autosomal recessive spastic paraplegia type 20,Autosomal recessive spastic paraplegia type 21,Autosomal recessive spastic paraplegia type 23,Autosomal recessive spastic paraplegia type 26,Autosomal recessive spastic paraplegia type 28,Autosomal recessive spastic paraplegia type 35,Autosomal recessive spastic paraplegia type 39,Autosomal recessive spastic paraplegia type 43,Autosomal recessive spastic paraplegia type 44,Autosomal recessive spastic paraplegia type 45,Autosomal recessive spastic paraplegia type 46,Autosomal recessive spastic paraplegia type 48,Autosomal recessive spastic paraplegia type 53,Autosomal recessive spastic paraplegia type 54,Autosomal recessive spastic paraplegia type 55,Autosomal recessive spastic paraplegia type 56,Autosomal recessive spastic paraplegia type 57,Autosomal recessive spastic paraplegia type 59,Autosomal recessive spastic paraplegia type 5A,Autosomal recessive spastic paraplegia type 60,Autosomal recessive spastic paraplegia type 61,Autosomal recessive spastic paraplegia type 62,Autosomal recessive spastic paraplegia type 63,Autosomal recessive spastic paraplegia type 64,Autosomal recessive spastic paraplegia type 66,Autosomal recessive spastic paraplegia type 67,Autosomal recessive spastic paraplegia type 69,Autosomal recessive spastic paraplegia type 70,Autosomal recessive spastic paraplegia type 71,Autosomal recessive spastic paraplegia type 74,Autosomal recessive spastic paraplegia type 75,Autosomal recessive spastic paraplegia type 76,Autosomal recessive spastic paraplegia type 77,Autosomal recessive spastic paraplegia type 78,Autosomal recessive spastic paraplegia type 9B,Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome,Autosomal recessive spondylocostal dysostosis,Autosomal recessive spondylometaphyseal dysplasia Megarbane type,Autosomal recessive Stickler syndrome,AUTOSOMAL RECESSIVE TYPICAL NEMALINE MYOPATHY,Autosomal Recessive Wiedemann Rautenstrauch Syndrome,Autosomal semi-dominant severe lipodystrophic laminopathy,Autosomal spastic paraplegia type 30,Autosomal spastic paraplegia type 58,Autosomal spastic paraplegia type 72,Autosomal systemic lupus erythematosus,Autosomal thrombocytopenia with normal platelets,Autosomal- Recessive Intellectual Disability MRT5,Autosomal-Dominant Hypotrichosis Simplex,Autosomal-dominant microcephaly associated with lymphedema and/or chorioretinopathy,Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin syndrome,Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia,Autosomal-Recessive Cerebellar Ataxia with Spasticity.,Autosomal-Recessive Complete Congenital Stationary Night Blindness,Autosomal-Recessive cone-Rod dystrophy,Autosomal-Recessive Disorder with Congenital Cataracts Hearing Loss and Low Serum Copper and Ceruloplasmin,Autosomal-Recessive Intellectual Disability and Microcephaly,Autosomal-Recessive microcephaly with chorioretinopathy.,Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction,AVASCULAR NECROSIS OF FEMORAL HEAD PRIMARY 1,AVASCULAR NECROSIS OF FEMORAL HEAD PRIMARY 2,Axenfeld anomaly,Axenfeld-Rieger syndrome,AXENFELD-RIEGER SYNDROME TYPE 1,AXENFELD-RIEGER SYNDROME TYPE 3,Axial Spondylometaphyseal Dysplasia,AXIN2-related attenuated familial adenomatous polyposis,Ayme-Gripp syndrome,AZOOSPERMIA OBSTRUCTIVE WITH NEPHROLITHIASIS,B-cell chronic lymphocytic leukemia,B-CELL CLL/LYMPHOMA 2,B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY,B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome,B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome,B4GALT1-CDG,B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome,BACHMANN-BUPP SYNDROME,BACTEREMIA SUSCEPTIBILITY TO 1,BACTEREMIA SUSCEPTIBILITY TO 2,Bacterial susceptibility due to TLR signaling pathway deficiency,Bainbridge-Ropers syndrome,BAKER-GORDON SYNDROME,Baller-Gerold syndrome,Bamforth-Lazarus syndrome,Band heterotopia,Bannayan-Riley-Ruvalcaba syndrome,BAP1-related tumor predisposition syndrome,Baraitser-Winter cerebrofrontofacial syndrome,Baraitser-Winter syndrome,BARAITSER-WINTER SYNDROME 1,Baraitser-Winter Syndrome 2,Baratela Scott Syndrome,Barber-Say syndrome,Bardet-Biedl syndrome,BARDET-BIEDL SYNDROME 1,BARDET-BIEDL SYNDROME 10,BARDET-BIEDL SYNDROME 11,BARDET-BIEDL SYNDROME 12,BARDET-BIEDL SYNDROME 13,Bardet-Biedl syndrome 14,Bardet-Biedl syndrome 15,BARDET-BIEDL SYNDROME 16,BARDET-BIEDL SYNDROME 17,Bardet-Biedl syndrome 18,Bardet-Biedl syndrome 19,BARDET-BIEDL SYNDROME 2,BARDET-BIEDL SYNDROME 20,BARDET-BIEDL SYNDROME 21,BARDET-BIEDL SYNDROME 3,BARDET-BIEDL SYNDROME 4,BARDET-BIEDL SYNDROME 5,BARDET-BIEDL SYNDROME 6,BARDET-BIEDL SYNDROME 7,BARDET-BIEDL SYNDROME 8,BARDET-BIEDL SYNDROME 9,BARDET-BIEDL SYNDROME TYPE 1,BARDET-BIEDL SYNDROME TYPE 10,BARDET-BIEDL SYNDROME TYPE 11,BARDET-BIEDL SYNDROME TYPE 12,BARDET-BIEDL SYNDROME TYPE 13,BARDET-BIEDL SYNDROME TYPE 15,BARDET-BIEDL SYNDROME TYPE 2,BARDET-BIEDL SYNDROME TYPE 3,BARDET-BIEDL SYNDROME TYPE 4,BARDET-BIEDL SYNDROME TYPE 5,BARDET-BIEDL SYNDROME TYPE 7,BARDET-BIEDL SYNDROME TYPE 8,BARDET-BIEDL SYNDROME TYPE 9,BARE LYMPHOCYTE SYNDROME TYPE I,BARE LYMPHOCYTE SYNDROME TYPE II,BARRETT ESOPHAGUS,BART-PUMPHREY SYNDROME,Barth syndrome,Bartsocas-Papas syndrome,BARTTER SYNDROME TYPE 1 ANTENATAL,BARTTER SYNDROME TYPE 2 ANTENATAL,BARTTER SYNDROME TYPE 3,BARTTER SYNDROME TYPE 4A,BARTTER SYNDROME TYPE 4A NEONATAL WITH SENSORINEURAL DEAFNESS,BARTTER SYNDROME TYPE 4B,BARTTER SYNDROME TYPE 4B NEONATAL WITH SENSORINEURAL DEAFNESS,Bartter syndrome type 5 antenatal transient,BASAL CELL CARCINOMA SUSCEPTIBILITY TO 1,BASAL CELL CARCINOMA SUSCEPTIBILITY TO 7,Basal cell nevus syndrome,BASAL GANGLIA CALCIFICATION IDIOPATHIC 1,BASAL GANGLIA CALCIFICATION IDIOPATHIC 4,BASAL GANGLIA CALCIFICATION IDIOPATHIC 5,BASAL GANGLIA CALCIFICATION IDIOPATHIC 6,BASAL GANGLIA CALCIFICATION IDIOPATHIC 7 AUTOSOMAL RECESSIVE,BASAL GANGLIA CALCIFICATION IDIOPATHIC 8 AUTOSOMAL RECESSIVE,BASAL LAMINAR DRUSEN,Basan syndrome,Basel-Vanagaite-Smirin-Yosef syndrome,BASILICATA-AKHTAR SYNDROME,Bathing suit ichthyosis,BCL11B-related developmental disorder monoallelic,Beare-Stevenson Cutis Gyrata syndrome,Beaulieu-Boycott-Innes syndrome,BECK-FAHRNER SYNDROME,BECKER MUSCULAR DYSTROPHY,Becker nevus syndrome,BECKWITH-WIEDEMANN SYNDROME,Beckwith-Wiedemann syndrome due to 11p15 microdeletion,Beckwith-Wiedemann syndrome due to CDKN1C mutation,Beckwith-Wiedemann syndrome due to imprinting defect of 11p15,Beckwith-Wiedemann syndrome due to NSD1 mutation,Behavioral variant of frontotemporal dementia,Behcet disease,Behr syndrome,Benign adult familial myoclonic epilepsy,BENIGN CHRONIC PEMPHIGUS,Benign familial infantile epilepsy,Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome,Benign familial mesial temporal lobe epilepsy,Benign familial neonatal epilepsy,Benign familial neonatal-infantile seizures,Benign hereditary chorea,BENIGN NEONATAL EPILEPSY TYPE 1,Benign paroxysmal torticollis of infancy,Benign recurrent intrahepatic cholestasis type 1,Benign recurrent intrahepatic cholestasis type 2,Benign Samaritan congenital myopathy,BENT BONE DYSPLASIA SYNDROME,BENTA disease,BERNARD-SOULIER SYNDROME,BERNARD-SOULIER SYNDROME TYPE A2 AUTOSOMAL DOMINANT,Best vitelliform macular dystrophy,BESTROPHINOPATHY AUTOSOMAL RECESSIVE,BETA-1-ADRENERGIC RECEPTOR,BETA-2-ADRENERGIC RECEPTOR,BETA-AMINOISOBUTYRIC ACIDURIA,BETA-GLUCOPYRANOSIDE TASTING,Beta-ketothiolase deficiency,BETA-MANNOSIDOSIS,Beta-propeller protein-associated neurodegeneration,Beta-sarcoglycan-related  limb-girdle muscular dystrophy R4,BETA-THALASSEMIA,BETA-THALASSEMIA DOMINANT INCLUSION BODY TYPE,BETA-THALASSEMIA INTERMEDIA,Beta-thalassemia major,Beta-thalassemia-X-linked thrombocytopenia syndrome,BETA-UREIDOPROPIONASE DEFICIENCY,BETHLEM MYOPATHY,Bethlem myopathy 1,BETHLEM MYOPATHY 2,BEUKES HIP DYSPLASIA,BH4-Deficient Hyperphenylalaninemia C,BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy,BICRA-related Developmental Disorder,Bicuspid Aortic Valve and Aortic Aneurysm,BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY,Bietti crystalline dystrophy,BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES,Bifid uvula,Bifunctional enzyme deficiency,Bilateral diffuse polymicrogyria,Bilateral frontoparietal polymicrogyria,Bilateral generalized polymicrogyria,Bilateral microtia-deafness-cleft palate syndrome,Bilateral multicystic dysplastic kidney,Bilateral parasagittal parieto-occipital polymicrogyria,Bilateral perisylvian polymicrogyria,Bilateral striopallidodentate calcinosis,Bile acid CoA ligase deficiency and defective amidation,BILE ACID CONJUGATION DEFECT 1,BILE ACID MALABSORPTION PRIMARY,BILE ACID SYNTHESIS DEFECT CONGENITAL 1,BILE ACID SYNTHESIS DEFECT CONGENITAL 2,BILE ACID SYNTHESIS DEFECT CONGENITAL 3,BILE ACID SYNTHESIS DEFECT CONGENITAL 4,BILE ACID SYNTHESIS DEFECT CONGENITAL 5,BILE ACID SYNTHESIS DEFECT CONGENITAL 6,Biliary atresia with splenic malformation syndrome,BILIRUBIN SERUM LEVEL OF QUANTITATIVE TRAIT LOCUS 1,Biotin-thiamine-responsive basal ganglia disease,BIOTINIDASE DEFICIENCY,Birbeck granule deficiency,Birdshot chorioretinopathy,BIRK-BAREL SYNDROME,Birk-Landau-Perez syndrome,Birt-Hogg-Dube syndrome,Bjornstad syndrome,Blackfan-Diamond anemia,Bladder Cancer,BLADDER DYSFUNCTION AUTONOMIC WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT,Bladder exstrophy,Bladder exstrophy plus,BLAU SYNDROME,Bleeding diathesis due to glycoprotein VI deficiency,Bleeding diathesis due to thromboxane synthesis deficiency,Bleeding disorder due to CalDAG-GEFI deficiency,Bleeding disorder due to P2Y12 defect,BLEEDING DISORDER PLATELET-TYPE 11,BLEEDING DISORDER PLATELET-TYPE 13 SUSCEPTIBILITY TO,BLEEDING DISORDER PLATELET-TYPE 15,BLEEDING DISORDER PLATELET-TYPE 16,BLEEDING DISORDER PLATELET-TYPE 17,BLEEDING DISORDER PLATELET-TYPE 18,BLEEDING DISORDER PLATELET-TYPE 19,BLEEDING DISORDER PLATELET-TYPE 20,Bleeding disorder platelet-type 21,BLEEDING DISORDER PLATELET-TYPE 22,BLEEDING DISORDER PLATELET-TYPE 8,Blepharo-cheilo-odontic syndrome,Blepharo-cheiro-dontic syndrome,BLEPHAROCHEILODONTIC SYNDROME 1,BLEPHAROCHEILODONTIC SYNDROME 2,Blepharophimosis ptosis and epicanthus inversus,Blepharophimosis ptosis and epicanthus inversus syndrome,Blepharophimosis- mental retardation,Blepharophimosis-intellectual disability syndrome MKB type,Blepharophimosis-intellectual disability syndrome SBBYS type,Blepharophimosis-ptosis-epicanthus inversus syndrome plus,Blepharophimosis-ptosis-epicanthus inversus syndrome type 1,Blepharophimosis-ptosis-epicanthus inversus syndrome type 2,BLEPHAROSPASM BENIGN ESSENTIAL SUSCEPTIBILITY TO,BLISTERING ACANTHOLYTIC OF ORAL AND LARYNGEAL MUCOSA,Blomstrand lethal chondrodysplasia,BLOOD GROUP CHIDO/RODGERS SYSTEM,BLOOD GROUP COLTON SYSTEM,BLOOD GROUP CROMER SYSTEM,Blood group dombrock system,BLOOD GROUP DUFFY SYSTEM,Blood group gerbich system,BLOOD GROUP GLOBOSIDE SYSTEM,BLOOD GROUP I SYSTEM,BLOOD GROUP INDIAN SYSTEM,BLOOD GROUP JOHN MILTON HAGEN SYSTEM,BLOOD GROUP JUNIOR SYSTEM,BLOOD GROUP LANGEREIS SYSTEM,BLOOD GROUP LEWIS SYSTEM,BLOOD GROUP MN,BLOOD GROUP P1PK SYSTEM P(1) PHENOTYPE INCLUDED,BLOOD GROUP Ss,BLOOD GROUP SYSTEM LANDSTEINER-WIENER,BLOOD GROUP VEL SYSTEM,BLOOD GROUP XG SYSTEM,BLOOD GROUP--DIEGO SYSTEM,BLOOD GROUP--FROESE,BLOOD GROUP--KELL SYSTEM,BLOOD GROUP--KIDD SYSTEM,BLOOD GROUP--LUTHERAN INHIBITOR,BLOOD GROUP--LUTHERAN SYSTEM,BLOOD GROUP--OK,BLOOD GROUP--SCIANNA SYSTEM,BLOOD GROUP--SWANN SYSTEM,BLOOD GROUP--WALDNER TYPE,BLOOD GROUP--WRIGHT ANTIGEN,Bloom syndrome,Bloom Syndrome like Disorder,BLUE CONE MONOCHROMACY,Blue cone monochromatism,Blue rubber bleb nevus,BMP4-associated malformations,BNAR syndrome,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4,BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9,Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency,BOERJESON-FORSSMAN-LEHMANN SYNDROME,Bohring-Opitz syndrome,BOMBAY PHENOTYPEPARA-BOMBAY PHENOTYPE INCLUDED,Bone fragility with contractures arterial rupture and deafness,BONE MARROW FAILURE SYNDROME 1,Bone marrow failure syndrome 2,BONE MARROW FAILURE SYNDROME 3,BONE MARROW FAILURE SYNDROME 4,BONE MARROW FAILURE SYNDROME 5,BONE MARROW FAILURE SYNDROME 6,Bone mineral density quantitative trait locus 1,BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 12,Bone mineral density quantitative trait locus 15,BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16,BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17,BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18,BOOMERANG DYSPLASIA,BOR syndrome,BORJESON-FORSSMAN-LEHMANN SYNDROME,Bosch-Boonstra optic atrophy syndrome,Bosch-boonstra-schaaf optic atrophy syndrome,BOSLEY-SALIH-ALORAINY SYNDROME,BOSMA ARHINIA MICROPHTHALMIA SYNDROME,BOTHNIA RETINAL DYSTROPHY,Boucher Neuhauser syndrome,BOWEN-CONRADI SYNDROME,BRACHYCEPHALY TRICHOMEGALY AND DEVELOPMENTAL DELAY,Brachydactyly type A1,BRACHYDACTYLY TYPE A1 C,BRACHYDACTYLY TYPE A1 D,Brachydactyly type A2,Brachydactyly type B1,Brachydactyly type B2,Brachydactyly type C,BRACHYDACTYLY TYPE D,BRACHYDACTYLY TYPE E,BRACHYDACTYLY TYPE E1,BRACHYDACTYLY TYPE E2,Brachydactyly-arterial hypertension syndrome,Brachydactyly-elbow wrist dysplasia syndrome,BRACHYDACTYLY-MENTAL RETARDATION SYNDROME,BRACHYDACTYLY-SYNDACTYLY SYNDROME,Brachydactyly-syndactyly Zhao type,BRACHYOLMIA TYPE 3,BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES,Brachyolmia-amelogenesis imperfecta syndrome,Brachytelephalangic chondrodysplasia punctata,Bradyopsia,BRAIN ABNORMALITIES NEURODEGENERATION AND DYSOSTEOSCLEROSIS,Brain atrophy Dandy Walker and Contractures,Brain calcification Rajab type,Brain demyelination due to methionine adenosyltransferase deficiency,Brain dopamine-serotonin vesicular transport disease,BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS,Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome,BRAIN SMALL VESSEL DISEASE 1 WITH OR WITHOUT OCULAR ANOMALIES,BRAIN SMALL VESSEL DISEASE 2,BRAIN SMALL VESSEL DISEASE 3,Brain-lung-thyroid syndrome,Branched-chain keto acid dehydrogenase kinase deficiency,BRANCHIOOCULOFACIAL SYNDROME,Branchiootic syndrome,BRANCHIOOTIC SYNDROME 1,BRANCHIOOTIC SYNDROME 3,BRANCHIOOTIC SYNDROME TYPE 3,BRANCHIOOTORENAL SYNDROME 1,BRANCHIOOTORENAL SYNDROME 2,BRANCHIOOTORENAL SYNDROME TYPE 1,branchiootorenal syndrome type 2,Branchioskeletogenital syndrome,Breast Cancer,BREAST-OVARIAN CANCER FAMILIAL SUSCEPTIBILITY TO 1,BREAST-OVARIAN CANCER FAMILIAL SUSCEPTIBILITY TO 2,BREAST-OVARIAN CANCER FAMILIAL SUSCEPTIBILITY TO 3,BREAST-OVARIAN CANCER FAMILIAL SUSCEPTIBILITY TO 4,BREASTS AND/OR NIPPLES APLASIA OR HYPOPLASIA OF 2,BRESEK syndrome,BRF1-related cerebellofaciodental syndrome,Brittle cornea syndrome,BRITTLE CORNEA SYNDROME 1,BRITTLE CORNEA SYNDROME 2,BRODY MYOPATHY,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3,BROOKE-SPIEGLER SYNDROME,Brown-Vialetto-Van laere syndrome,BROWN-VIALETTO-VAN LAERE SYNDROME 1,BROWN-VIALETTO-VAN LAERE SYNDROME 2,BRPF1 associated syndromic intellectual disability with ptosis,Bruck syndrome,Bruck syndrome 1,BRUCK SYNDROME 2,Bruck syndrome type 2,Brugada syndrome,BRUGADA SYNDROME 1,BRUGADA SYNDROME 2,BRUGADA SYNDROME 3,BRUGADA SYNDROME 4,BRUGADA SYNDROME 5,BRUGADA SYNDROME 6,BRUGADA SYNDROME 7,BRUGADA SYNDROME 8,BRUGADA SYNDROME 9,BRUNNER SYNDROME,BUDD-CHIARI SYNDROME,Bullous diffuse cutaneous mastocytosis,Bullous pemphigoid,BURKITT LYMPHOMA,BURN-MCKEOWN SYNDROME,BURULI ULCER SUSCEPTIBILITY TO,Buschke-Ollendorff syndrome,Butterfly-shaped pigment dystrophy,BUTYRYLCHOLINESTERASE DEFICIENCY,BVES-related limb-girdle muscular dystrophy,C Syndrome,C1 inhibitor deficiency,C11ORF73-related autosomal recessive hypomyelinating leukodystrophy,C1q DEFICIENCY,C3 glomerulonephritis,C3 glomerulopathy,C3HEX ABILITY TO SMELL,CACNA1G-related developmental disorder monoallelic,CAD-CDG,CADDS,CAFFEY DISEASE,CALCIFICATION OF JOINTS AND ARTERIES,Calpain-3-related  limb-girdle muscular dystrophy R1,CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY,CAMOS syndrome,CAMPOMELIC DYSPLASIA,CAMPTODACTYLY TALL STATURE AND HEARING LOSS SYNDROME,CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME,Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome,Camptodactyly-tall stature-scoliosis-hearing loss syndrome,CAMPTOSYNPOLYDACTYLY COMPLEX,CAMURATI-ENGELMANN DISEASE,CANAVAN DISEASE,CANCER ALOPECIA PIGMENT DYSCRASIA ONYCHODYSTROPHY AND KERATODERMA,CANDIDIASIS FAMILIAL 2,CANDIDIASIS FAMILIAL 4,CANDIDIASIS FAMILIAL 6,CANDIDIASIS FAMILIAL 8,CANDIDIASIS FAMILIAL 9,CANTU SYNDROME,Cantu syndrome HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA,Cap myopathy,CAPICUA DROSOPHILA HOMOLOG OF,Capillary malformation of the lower lip lymphatic malformation of face and neck asymmetry of face and limbs and partial/generalized overgrowth,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2,Capillary malformations congenital,CARBAMOYL PHOSPHATE SYNTHETASE 1 DEFICIENCY,CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY HYPERAMMONEMIA DUE TO,Carbamoyl-phosphate synthetase 1 deficiency,CARBONIC ANHYDRASE VA DEFICIENCY HYPERAMMONEMIA DUE TO,CARBOXYPEPTIDASE N DEFICIENCY,Carcinoid syndrome,Cardiac arrhythmia ankyrin B-related,CARDIAC CONDUCTION DEFECT SUDDEN CARDIAC DEATH INCLUDED,Cardiac conduction disease with or without dilated cardiomyopathy,CARDIAC FACIAL AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY,CARDIAC VALVULAR DEFECT DEVELOPMENTAL,Cardiac valvular dysplasia X-linked,CARDIAC-UROGENITAL SYNDROME,Cardiac-valvular Ehlers-Danlos syndrome,CARDIOACROFACIAL DYSPLASIA 1,CARDIOACROFACIAL DYSPLASIA 2,CARDIOFACIOCUTANEOUS SYNDROME,CARDIOFACIOCUTANEOUS SYNDROME 1,CARDIOFACIOCUTANEOUS SYNDROME 2,CARDIOFACIOCUTANEOUS SYNDROME 3,CARDIOFACIOCUTANEOUS SYNDROME 4,CARDIOFACIONEURODEVELOPMENTAL SYNDROME,CARDIOMYOPATHY DILATED 1A,CARDIOMYOPATHY DILATED 1AA WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION,CARDIOMYOPATHY DILATED 1BB,CARDIOMYOPATHY DILATED 1C WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION,CARDIOMYOPATHY DILATED 1CC,CARDIOMYOPATHY DILATED 1D,CARDIOMYOPATHY DILATED 1DD,CARDIOMYOPATHY DILATED 1E,CARDIOMYOPATHY DILATED 1EE,CARDIOMYOPATHY DILATED 1FF,CARDIOMYOPATHY DILATED 1G,CARDIOMYOPATHY DILATED 1GG,CARDIOMYOPATHY DILATED 1HH,CARDIOMYOPATHY DILATED 1I,CARDIOMYOPATHY DILATED 1II,CARDIOMYOPATHY DILATED 1J,CARDIOMYOPATHY DILATED 1JJ,CARDIOMYOPATHY DILATED 1KK,CARDIOMYOPATHY DILATED 1L,CARDIOMYOPATHY DILATED 1M,Cardiomyopathy dilated 1nn,CARDIOMYOPATHY DILATED 1O,CARDIOMYOPATHY DILATED 1P,CARDIOMYOPATHY DILATED 1R,CARDIOMYOPATHY DILATED 1S,Cardiomyopathy dilated 1u,CARDIOMYOPATHY DILATED 1V,CARDIOMYOPATHY DILATED 1W,CARDIOMYOPATHY DILATED 1X,CARDIOMYOPATHY DILATED 1Y,CARDIOMYOPATHY DILATED 1Z,CARDIOMYOPATHY DILATED 2A,Cardiomyopathy dilated 2b,CARDIOMYOPATHY DILATED 2C,CARDIOMYOPATHY DILATED 3B,CARDIOMYOPATHY DILATED WITH HYPERGONADOTROPIC HYPOGONADISM,CARDIOMYOPATHY DILATED WITH WOOLLY HAIR AND KERATODERMA,Cardiomyopathy dilated with woolly hair keratoderma and tooth agenesis,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 1,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 10,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 11,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 12,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 13,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 14,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 15,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 16,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 17,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 18,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 2,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 20,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 25,Cardiomyopathy familial hypertrophic 26,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 27,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 3,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 4,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 6,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 7,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 8,CARDIOMYOPATHY FAMILIAL HYPERTROPHIC 9,CARDIOMYOPATHY FAMILIAL RESTRICTIVE 1,CARDIOMYOPATHY FAMILIAL RESTRICTIVE 3,Cardiomyopathy-hypotonia-lactic acidosis syndrome,CARDIOSPONDYLOCARPOFACIAL SYNDROME,CAREY-FINEMAN-ZITER SYNDROME,Carney complex,Carney complex type 1,CARNEY COMPLEX VARIANT,Carney complex-trismus-pseudocamptodactyly syndrome,Carney-Stratakis syndrome,CARNITINE DEFICIENCY SYSTEMIC PRIMARY,Carnitine palmitoyl transferase 1A deficiency,Carnitine palmitoyl transferase II deficiency myopathic form,Carnitine palmitoyl transferase II deficiency neonatal form,Carnitine palmitoyl transferase II deficiency severe infantile form,CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY INFANTILE,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY LETHAL NEONATAL,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY MYOPATHIC STRESS-INDUCED,CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY,Caroli disease,CAROTID INTIMAL MEDIAL THICKNESS 1,Carpal tunnel syndrome 2,CARPENTER SYNDROME,CARPENTER SYNDROME 1,CARPENTER SYNDROME 2,CARTILAGE-HAIR HYPOPLASIA,Carvajal syndrome,CASPASE 8 DEFICIENCY,CATARACT 1 MULTIPLE TYPES,CATARACT 10 MULTIPLE TYPES,CATARACT 11 MULTIPLE TYPES,CATARACT 12 MULTIPLE TYPES,CATARACT 13 WITH ADULT i PHENOTYPE,CATARACT 14 MULTIPLE TYPES,CATARACT 15 MULTIPLE TYPES,CATARACT 16 MULTIPLE TYPES,CATARACT 17 MULTIPLE TYPES,CATARACT 17 MULTIPLE TYPES MONOALLELIC,CATARACT 18,CATARACT 19 MULTIPLE TYPES,CATARACT 2 MULTIPLE TYPES,CATARACT 20 MULTIPLE TYPES,Cataract 21 multiple types,CATARACT 22 MULTIPLE TYPES,CATARACT 23 MULTIPLE TYPES,CATARACT 3 MULTIPLE TYPES,CATARACT 30 MULTIPLE TYPES,CATARACT 31 MULTIPLE TYPES,CATARACT 33 MULTIPLE TYPES,CATARACT 34 MULTIPLE TYPES,CATARACT 36,CATARACT 38,Cataract 39 multiple types,CATARACT 4 MULTIPLE TYPES,CATARACT 40,Cataract 41,CATARACT 42,CATARACT 43,Cataract 44,CATARACT 45,CATARACT 46 JUVENILE-ONSET WITH OR WITHOUT ARRHYTHMIC CARDIOMYOPATHY,CATARACT 47,CATARACT 48,Cataract 5 multiple types,Cataract 6 multiple types,CATARACT 9 MULTIPLE TYPES,CATARACT AUTOSOMAL DOMINANT BFSP2-RELATED,CATARACT AUTOSOMAL RECESSIVE CONGENITAL 1,Cataract autosomal recessive congenital 2,CATARACT CONGENITAL AUTOSOMAL RECESSIVE TYPE 4,CATARACT CONGENITAL CERULEAN TYPE 2,CATARACT CONGENITAL NUCLEAR AUTOSOMAL RECESSIVE 2,CATARACT CONGENITAL ZONULAR WITH SUTURAL OPACITIES,CATARACT COPPOCK-LIKE,CATARACT NUCLEAR,CATARACT POSTERIOR POLAR TYPE 2,CATARACT ZONULAR PULVERULENT CATARACT TYPE 3,Cataract-glaucoma syndrome,Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome,Cataract-intellectual disability-hypogonadism syndrome,Cataract-microcornea syndrome,Cataracts growth hormone deficiency sensory neuropathy sensorineural hearing loss and skeletal dysplasia,CATECHOL-O-METHYLTRANSFERASE,Catecholaminergic polymorphic ventricular tachycardia,Catel-Manzke syndrome,Cathepsin A-related arteriopathy-strokes-leukoencephalopathy,CATIFA SYNDROME,caudal duplication anomaly,Caudal regression sequence,CAUSE OF EARLY-ONSET MYOPATHY WITH FATAL CARDIOMYOPATHY,CAVITARY OPTIC DISC ANOMALIES,CCDC115-CDG,CCDC32-associated neurodevelopmental syndrome,CD8 DEFICIENCY FAMILIAL,CDC40-related Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly,CDC42-related Neurodevelopmental Disorder,CDC42BPB-related Neurodevelopmental Disorder,CDK19-associated Intellectual Disability and Epileptic Encephalopathy,CDKL5-related epileptic encephalopathy,CEBALID SYNDROME,CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome,CEDNIK syndrome,CELF2-related neurodevelopmental disorder,CELIAC DISEASE SUSCEPTIBILITY TO 3,CELIAC DISEASE SUSCEPTIBILITY TO 4,CENANI-LENZ SYNDACTYLY SYNDROME,Cenani-Lenz syndrome,CENPJ-related developmental disorder,Central areolar choroidal dystrophy,Central core disease,CENTRAL CORE DISEASE OF MUSCLE,central hypothyroidism and testicular enlargement,CENTRAL HYPOVENTILATION SYNDROME CONGENITAL,Central hypoventilation syndrome congenital with or without Hirschsprung disease,Centronuclear Myopathy 2,CENTRONUCLEAR MYOPATHY AUTOSOMAL MODIFIER OF,Centronuclear myopathy with dilated cardiomyopathy,CEP152-related Developmental Disorder,CEREBELLAR ATAXIA AREFLEXIA PES CAVUS OPTIC ATROPHY AND SENSORINEURAL HEARING LOSS,CEREBELLAR ATAXIA CAYMAN TYPE,CEREBELLAR ATAXIA DEAFNESS AND NARCOLEPSY AUTOSOMAL DOMINANT,CEREBELLAR ATAXIA MENTAL RETARDATION AND DYSEQUILIBRIUM SYNDROME 1,CEREBELLAR ATAXIA MENTAL RETARDATION AND DYSEQUILIBRIUM SYNDROME 2,Cerebellar ataxia mental retardation and dysequilibrium syndrome 3,Cerebellar ataxia mental retardation and dysequilibrium syndrome 4,CEREBELLAR ATAXIA MENTAL RETARDATION AND DYSEQUILIBRIUM SYNDROME TYPE 1,CEREBELLAR ATAXIA MENTAL RETARDATION AND DYSEQUILIBRIUM SYNDROME TYPE 3,Cerebellar ataxia neuropathy and vestibular areflexia syndrome,CEREBELLAR ATAXIA NONPROGRESSIVE WITH MENTAL RETARDATION,Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome,Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome,Cerebellar ataxia-hypogonadism syndrome,CEREBELLAR ATROPHY DEVELOPMENTAL DELAY AND SEIZURES,CEREBELLAR ATROPHY VISUAL IMPAIRMENT AND PSYCHOMOTOR RETARDATION,CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY,Cerebellar Atrophy with Spinal Motor Neuronopathy,Cerebellar dysplasia with cysts with or without retinal dystrophy,CEREBELLAR HYPOPLASIA/ATROPHY EPILEPSY AND GLOBAL DEVELOPMENTAL DELAY,CEREBELLAR OCULAR CRANIOFACIAL AND GENITAL SYNDROME,cerebellar-facial-dental syndrome,Cerebello-Oculo-Facio-Genital syndrome,CEREBELLOFACIODENTAL SYNDROME,CEREBRAL AMYLOID ANGIOPATHY APP-RELATED,CEREBRAL AMYLOID ANGIOPATHY CST3-RELATED,CEREBRAL AMYLOID ANGIOPATHY ITM2B-RELATED 1,CEREBRAL AMYLOID ANGIOPATHY ITM2B-RELATED 2,CEREBRAL ARTERIOPATHY AUTOSOMAL DOMINANT WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY TYPE 1,Cerebral arteriopathy autosomal dominant with subcortical infarcts and leukoencephalopathy type 2,CEREBRAL ARTERIOPATHY AUTOSOMAL RECESSIVE WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY,Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy,Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy,CEREBRAL CAVERNOUS MALFORMATIONS,CEREBRAL CAVERNOUS MALFORMATIONS 2,CEREBRAL CAVERNOUS MALFORMATIONS 3,CEREBRAL CAVERNOUS MALFORMATIONS TYPE 1,CEREBRAL CAVERNOUS MALFORMATIONS TYPE 3,CEREBRAL CREATINE DEFICIENCY SYNDROME 1,CEREBRAL CREATINE DEFICIENCY SYNDROME 2,CEREBRAL CREATINE DEFICIENCY SYNDROME 3,Cerebral dysgenesis neuropathy ichthyosis and palmoplantar keratoderma syndrome,CEREBRAL PALSY SPASTIC QUADRIPLEGIC 1,Cerebral palsy spastic quadriplegic 2,Cerebral palsy spastic quadriplegic 3,CEREBRAL PALSY SPASTIC QUADRIPLEGIC TYPE 1,CEREBRAL PALSY SPASTIC QUADRIPLEGIC TYPE 2,CEREBRAL PALSY SPASTIC QUADRIPLEGIC TYPE 3,Cerebral palsy spastic quadriplegic type 4,cerebral palsy spastic quadriplegic type 5,Cerebral palsy spastic quadriplegic type 6,Cerebral sinovenous thrombosis,Cerebro-costo-mandibular syndrome,Cerebro-facio-articular syndrome,Cerebro-facio-thoracic dysplasia,CEREBRO-OCULO-FACIO-SKELETAL SYNDROME TYPE 2,CEREBROOCULOFACIOSKELETAL SYNDROME 1,CEREBROOCULOFACIOSKELETAL SYNDROME 2,CEREBROOCULOFACIOSKELETAL SYNDROME 3,CEREBROOCULOFACIOSKELETAL SYNDROME 4,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2,CEREBROTENDINOUS XANTHOMATOSIS,Cernunnos-XLF deficiency,CEROID LIPOFUSCINOSIS NEURONAL 1,CEROID LIPOFUSCINOSIS NEURONAL 10,CEROID LIPOFUSCINOSIS NEURONAL 11,CEROID LIPOFUSCINOSIS NEURONAL 13,CEROID LIPOFUSCINOSIS NEURONAL 2,CEROID LIPOFUSCINOSIS NEURONAL 3,CEROID LIPOFUSCINOSIS NEURONAL 4A AUTOSOMAL RECESSIVE,CEROID LIPOFUSCINOSIS NEURONAL 4B AUTOSOMAL DOMINANT,CEROID LIPOFUSCINOSIS NEURONAL 5,CEROID LIPOFUSCINOSIS NEURONAL 6,CEROID LIPOFUSCINOSIS NEURONAL 7,CEROID LIPOFUSCINOSIS NEURONAL 8,CEROID LIPOFUSCINOSIS NEURONAL 8 NORTHERN EPILEPSY VARIANT,Ceroid lipofuscinosis neuronal Kufs type adult onset,Cerulean cataract,Cervical Cancer,Cervical spina bifida aperta,Cervical spina bifida cystica,Cervicothoracic spina bifida aperta,Cervicothoracic spina bifida cystica,CFC1-Related Conotruncal Heart Malformations,CFHR5 DEFICIENCY,CHANARIN-DORFMAN SYNDROME,CHAND SYNDROME,Channelopathy-associated congenital insensitivity to pain,CHAR SYNDROME,CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS,CHARCOT-MARIE-TOOTH DISEASE AXONAL AUTOSOMAL DOMINANT TYPE 2A2A,CHARCOT-MARIE-TOOTH DISEASE AXONAL AUTOSOMAL RECESSIVE TYPE 2A2B,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2A1,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2B,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2B1,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2B2,Charcot-Marie-Tooth disease axonal type 2CC,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2D,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2DD,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2E,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2EE,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2F,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2I,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2J,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2K,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2L,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2N,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2O,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2P,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2Q,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2R,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2S,Charcot-Marie-Tooth disease axonal type 2t,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2U,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2V,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2W,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2X,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2Y,CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2Z,Charcot-Marie-Tooth disease axonal with vocal cord paresis autosomal recessive,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1A,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1B,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1C,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1D,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1F,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1G,CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 4F,CHARCOT-MARIE-TOOTH DISEASE DOMINANT INTERMEDIATE B,CHARCOT-MARIE-TOOTH DISEASE DOMINANT INTERMEDIATE C,CHARCOT-MARIE-TOOTH DISEASE DOMINANT INTERMEDIATE D,CHARCOT-MARIE-TOOTH DISEASE DOMINANT INTERMEDIATE E,Charcot-Marie-Tooth disease dominant intermediate F,CHARCOT-MARIE-TOOTH DISEASE DOMINANT INTERMEDIATE G,CHARCOT-MARIE-TOOTH DISEASE RECESSIVE INTERMEDIATE A,CHARCOT-MARIE-TOOTH DISEASE RECESSIVE INTERMEDIATE B,CHARCOT-MARIE-TOOTH DISEASE RECESSIVE INTERMEDIATE C,Charcot-Marie-Tooth disease recessive intermediate d,Charcot-Marie-Tooth disease type 1A,Charcot-Marie-Tooth disease type 1B,Charcot-Marie-Tooth disease type 1C,Charcot-Marie-Tooth disease type 1D,Charcot-Marie-Tooth disease type 1E,Charcot-Marie-Tooth disease type 1F,Charcot-Marie-Tooth disease type 2B1,Charcot-Marie-Tooth disease type 2B2,Charcot-Marie-Tooth disease type 2B5,Charcot-Marie-Tooth disease type 2H,Charcot-Marie-Tooth disease type 2P,Charcot-Marie-Tooth disease type 2R,Charcot-Marie-Tooth disease type 2S,Charcot-Marie-Tooth disease type 2T,Charcot-Marie-Tooth disease type 4A,CHARCOT-MARIE-TOOTH DISEASE TYPE 4B1,Charcot-Marie-Tooth disease type 4B2,Charcot-Marie-Tooth disease type 4B3,Charcot-Marie-Tooth disease type 4C,Charcot-Marie-Tooth disease type 4D,Charcot-Marie-Tooth disease type 4E,Charcot-Marie-Tooth disease type 4F,Charcot-Marie-Tooth disease type 4G,Charcot-Marie-Tooth disease type 4H,Charcot-Marie-Tooth disease type 4J,CHARCOT-MARIE-TOOTH DISEASE TYPE 4K,CHARCOT-MARIE-TOOTH DISEASE X-LINKED DOMINANT 1,Charcot-Marie-Tooth disease X-linked dominant 6,CHARCOT-MARIE-TOOTH DISEASE X-LINKED RECESSIVE 4 WITH OR WITHOUTCEREBELLAR ATAXIA,CHARCOT-MARIE-TOOTH DISEASE X-LINKED RECESSIVE 5,CHARCOT-MARIE-TOOTH DISEASE X-LINKED RECESSIVE TYPE 5,CHARGE SYNDROME,CHD1-related neurodevelopment disorder,Chediak-Higashi syndrome,CHEMOKINE CC MOTIF LIGAND 2,CHERUBISM,CHILBLAIN LUPUS 1,CHILBLAIN LUPUS 2,CHILD SYNDROME,Childhood absence epilepsy,childhood absence epilepsy type 5,Childhood apraxia of speech,Childhood encephalopathy due to thiamine pyrophosphokinase deficiency,Childhood overgrowth,Childhood-onset autosomal recessive myopathy with external ophthalmoplegia,Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia,Childhood-onset basal ganglia degeneration syndrome,Childhood-onset benign chorea with striatal involvement,Childhood-Onset Chorea with Bilateral Striatal Lesions,Childhood-Onset Dystonia and Optic Atrophy,Childhood-onset hypogammaglobulinemia,Childhood-onset hypophosphatasia,Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder,Childhood-onset nemaline myopathy,Childhood-Onset Neurodegeneration,Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome,Childhood-Onset Slowly Progressive Nemaline Myopathy,Childhood-onset spasticity with hyperglycinemia,CHIME syndrome,CHITAYAT SYNDROME,Chitayat syndrome: hyperphalangism characteristic facies hallux valgus and bronchomalacia,CHITOTRIOSIDASE DEFICIENCY,Choanal atresia and lymphedema,Cholangiocarcinoma,Cholestasis benign recurrent intrahepatic 1,CHOLESTASIS BENIGN RECURRENT INTRAHEPATIC 2,CHOLESTASIS INTRAHEPATIC OF PREGNANCY 1,Cholestasis intrahepatic of pregnancy 3,CHOLESTASIS PROGRESSIVE FAMILIAL INTRAHEPATIC 1,CHOLESTASIS PROGRESSIVE FAMILIAL INTRAHEPATIC 2,CHOLESTASIS PROGRESSIVE FAMILIAL INTRAHEPATIC 3,CHOLESTASIS PROGRESSIVE FAMILIAL INTRAHEPATIC 4,CHOLESTASIS PROGRESSIVE FAMILIAL INTRAHEPATIC 5,Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia,Cholesterol-ester transfer protein deficiency,Cholesteryl ester storage disease,CHONDROCALCINOSIS 2,Chondrodysplasia Blomstrand type,CHONDRODYSPLASIA GREBE TYPE,Chondrodysplasia Punctata 1 X-Linked,Chondrodysplasia punctata 1 X-linked recessive,Chondrodysplasia Punctata 2 X-Linked,CHONDRODYSPLASIA PUNCTATA 2 X-LINKED DOMINANT,CHONDRODYSPLASIA WITH JOINT DISLOCATIONS GPAPP TYPE,Chondrodysplasia with joint dislocations GRAPP type,Chondrodysplasia with multiple dislocations and amelogenesis imperfecta,Chondrodysplasia with platyspondyly distinctive brachydactyly hydrocephaly and microphthalmia,Chondrodysplasia-disorder of sex development syndrome,Chondromyxoid fibroma,CHONDROSARCOMA,CHONDROSARCOMA EXTRASKELETAL MYXOID,CHOPS SYNDROME,Chordoma,CHOREA BENIGN HEREDITARY,Chorea childhood-onset with psychomotor retardation,CHOREOACANTHOCYTOSIS,CHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM WITH OR WITHOUT PULMONARY DYSFUNCTION,CHOREOATHETOSIS HYPOTHYROIDISM AND NEONATAL RESPIRATORY DISTRESS,Choroid plexus carcinoma,CHOROIDAL DYSTROPHY CENTRAL AREOLAR 1,CHOROIDAL DYSTROPHY CENTRAL AREOLAR 2,CHOROIDEREMIA,Christianson syndrome,CHRNA2-RELATED NOCTURNAL FRONTAL LOBE EPILEPSY AUTOSOMAL DOMINANT,CHRNA3-related congenital anomalies of the kidney and urinary tract,CHRNB1-related congenital myaesthenia biallelic,CHRNB1-related congenital myaesthenia monoallelic,Chrnb2-Related nocturnal frontal lobe epilepsy autosomal dominant,Chromophobe renal cell carcinoma,Chromosome 11p15.5-Related Russell-Silver Syndrome,CHROMOSOME 15q13.3 DELETION SYNDROME,Chromosome 17q21.31 microdeletion syndrome,CHROMOSOME 1q21.1 DELETION SYNDROME 1.35-MB,CHROMOSOME 2p16.3 DELETION SYNDROMESCHIZOPHRENIA 17 INCLUDED,CHROMOSOME 2q37 DELETION SYNDROME,CHROMOSOME 5q DELETION SYNDROME,CHROMOSOME Xq26.3 DUPLICATION SYNDROME,Chromosome Xq28 duplication syndrome,CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA,Chronic atrial and intestinal dysrhythmia syndrome,Chronic beryllium disease,Chronic enteropathy associated with SLCO2A1 gene,Chronic eosinophilic leukemia,Chronic granulomatous disease,Chronic infantile diarrhea due to guanylate cyclase 2C overactivity,Chronic lymphoproliferative disorder of natural killer cells,Chronic mast cell leukemia,Chronic mucocutaneous candidiasis,Chronic myeloid leukemia,Chronic myelomonocytic leukemia,Chronic myeloproliferative disease unclassifiable,Chronic neutrophilic leukemia,Chronic respiratory distress with surfactant metabolism deficiency,CHST3-related skeletal dysplasia,CHUDLEY-MCCULLOUGH SYNDROME,CHUNG-JANSEN SYNDROME,Chuvash erythrocytosis,CHYLOMICRON RETENTION DISEASE,CIDEC-related familial partial lipodystrophy,CILIARY DYSKINESIA PRIMARY 1,CILIARY DYSKINESIA PRIMARY 10,CILIARY DYSKINESIA PRIMARY 11,CILIARY DYSKINESIA PRIMARY 12,CILIARY DYSKINESIA PRIMARY 13,Ciliary dyskinesia primary 14,Ciliary dyskinesia primary 15,CILIARY DYSKINESIA PRIMARY 16,CILIARY DYSKINESIA PRIMARY 17,CILIARY DYSKINESIA PRIMARY 18,CILIARY DYSKINESIA PRIMARY 19,CILIARY DYSKINESIA PRIMARY 2,CILIARY DYSKINESIA PRIMARY 20,CILIARY DYSKINESIA PRIMARY 21,CILIARY DYSKINESIA PRIMARY 22,CILIARY DYSKINESIA PRIMARY 23,CILIARY DYSKINESIA PRIMARY 24,CILIARY DYSKINESIA PRIMARY 25,Ciliary dyskinesia primary 26,CILIARY DYSKINESIA PRIMARY 27,Ciliary dyskinesia primary 28,CILIARY DYSKINESIA PRIMARY 29,CILIARY DYSKINESIA PRIMARY 3,Ciliary dyskinesia primary 30,CILIARY DYSKINESIA PRIMARY 32,Ciliary dyskinesia primary 33,CILIARY DYSKINESIA PRIMARY 34,CILIARY DYSKINESIA PRIMARY 35,CILIARY DYSKINESIA PRIMARY 36 X-LINKED,CILIARY DYSKINESIA PRIMARY 37,CILIARY DYSKINESIA PRIMARY 38,CILIARY DYSKINESIA PRIMARY 39,CILIARY DYSKINESIA PRIMARY 40,CILIARY DYSKINESIA PRIMARY 41,CILIARY DYSKINESIA PRIMARY 42,CILIARY DYSKINESIA PRIMARY 43,CILIARY DYSKINESIA PRIMARY 44,CILIARY DYSKINESIA PRIMARY 45,CILIARY DYSKINESIA PRIMARY 5,CILIARY DYSKINESIA PRIMARY 6,CILIARY DYSKINESIA PRIMARY 7,CILIARY DYSKINESIA PRIMARY 9,Ciliopathy-related syndromic intellectual disability,CIMDAG Syndrome biallelic,CIMDAG Syndrome monoallelic,CINCA SYNDROME,Circumferential Skin Creases Kunze Type,CIRRHOSIS FAMILIALCIRRHOSIS FAMILIAL WITH PULMONARY HYPERTENSION INCLUDED,Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome,CITRULLINEMIA CLASSIC,Citrullinemia Type I,Citrullinemia type II,CITRULLINEMIA TYPE II NEONATAL-ONSET,CK SYNDROME,Clark-Baraitser syndrome,Class I glucose-6-phosphate dehydrogenase deficiency,Classic Bartter syndrome,Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency salt wasting form,Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency simple virilizing form,Classic congenital lipoid adrenal hyperplasia due to STAR deficency,Classic galactosemia,Classic glucose transporter type 1 deficiency syndrome,Classic hairy cell leukemia,Classic Hodgkin lymphoma nodular sclerosis type,Classic homocystinuria,Classic maple syrup urine disease,Classic multiminicore myopathy,Classic mycosis fungoides,Classic pantothenate kinase associated neurodegeneration,Classic phenylketonuria,Classic progressive supranuclear palsy syndrome,Classical Ehlers-Danlos syndrome,Classical-like Ehlers-Danlos syndrome type 1,Classical-like Ehlers-Danlos syndrome type 2,CLCN4-related X-linked intellectual disability syndrome,CLCN6-related Developmental Disorder,CLCN7-Related Osteopetrosis,Clear cell papillary renal cell carcinoma,Clear cell renal carcinoma,Clear cell sarcoma of kidney,Cleft hard palate,Cleft Lip +/- Cleft Palate,Cleft lip and alveolus,Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome,Cleft lip/palate,CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME,CLEFT PALATE CARDIAC DEFECTS AND MENTAL RETARDATION,CLEFT PALATE PROLIFERATIVE RETINOPATHY AND DEVELOPMENTAL DELAY,Cleft palate psychomotor retardation and distinctive facial features,Cleft palate with or without ankyloglossia X-linked,Cleft palate X-linked,Cleft velum,CLEIDOCRANIAL DYSPLASIA,CLEIDOCRANIAL DYSPLASIA WITH MICROGNATHIA ABSENT THUMBS AND DISTAL APHALANGIA YUNIS-VARON SYNDROME,CLN1 disease,CLN10 disease,CLN11 disease,CLN13 disease,CLN2 disease,CLN3 disease,CLN4A disease,CLN4B disease,CLN5 disease,CLN6 disease,CLN7 disease,CLN8 disease,CLOUSTON SYNDROME,CLOVES syndrome,CLOVES: CONGENITAL LIPOMATOUS OVERGROWTH VASCULAR MALFORMATIONS AND EPIDERMAL NEVI,Clubbing with skeletal dysplasia inc acroosteolysis,CLUBFOOT CONGENITAL WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY,CNNM2-related neurodevelopmental disorder with hypomagnesemia,CNOT1-related neurodevelopmental disorder,CNOT3 syndrome,COACH SYNDROM,COACH SYNDROME 1,COACH SYNDROME 2,COACH SYNDROME 3,COASY protein-associated neurodegeneration,Coats disease,Coats Plus,Coats plus syndrome,Cobalamin Disorder,Cobblestone brain malformation without muscular or ocular abnormalities,Cobblestone Lissencephaly,Cobblestone lissencephaly without muscular or ocular involvement,Cockayne syndrome A,COCKAYNE SYNDROME B,Cockayne syndrome type 1,Cockayne syndrome type 2,Cockayne syndrome type 3,Cockayne syndrome type A,Cocoon syndrome,CODAS syndrome,Coenzyme Q10 deficiency,COENZYME Q10 DEFICIENCY PRIMARY 1,COENZYME Q10 DEFICIENCY PRIMARY 2,COENZYME Q10 DEFICIENCY PRIMARY 3,COENZYME Q10 DEFICIENCY PRIMARY 4,COENZYME Q10 DEFICIENCY PRIMARY 5,COENZYME Q10 DEFICIENCY PRIMARY 6,COENZYME Q10 DEFICIENCY PRIMARY 7,Coenzyme Q10 deficiency primary 8,COENZYME Q10 DEFICIENCY PRIMARY 9,Coffin Siris,Coffin Siris like disorder,COFFIN SIRIS SYNDROME,COFFIN-LOWRY SYNDROME,Coffin-Lowry Syndrome 2 RPS6KA3 XLD,Coffin-Lowry Syndrome 2 RPS6KA3 XLR,COFFIN-SIRIS SYNDROME,COFFIN-SIRIS SYNDROME 1,COFFIN-SIRIS SYNDROME 10,COFFIN-SIRIS SYNDROME 11,COFFIN-SIRIS SYNDROME 2,COFFIN-SIRIS SYNDROME 3,COFFIN-SIRIS SYNDROME 4,COFFIN-SIRIS SYNDROME 5,COFFIN-SIRIS SYNDROME 6,COFFIN-SIRIS SYNDROME 7,COFFIN-SIRIS SYNDROME 8,COFFIN-SIRIS SYNDROME 9,COFS syndrome,COG1-CDG,COG2-CDG,COG4-CDG,COG5-CDG,COG6-CGD,COG7-CDG,COG8-CDG,Cognitive impairment with or without cerebellar ataxia,Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome,Cohen syndrome,Cohen-Gibson syndrome,Cohesinopathy,COL1A1-RELATED OSTEOGENESIS IMPERFECTA,COL4A1-related familial vascular leukoencephalopathy,COL6A1 associated myopathy,COLCHICINE RESISTANCE,Cold-induced sweating syndrome,Cold-induced sweating syndrome type 1 (CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa,Cole disease,COLE-CARPENTER SYNDROME,COLE-CARPENTER SYNDROME 1,COLE-CARPENTER SYNDROME 2,COLOBOMA CONGENITAL HEART DISEASE ICHTHYOSIFORM DERMATOSIS MENTALRETARDATION AND EAR ANOMALIES SYNDROME,COLOBOMA OCULAR AUTOSOMAL DOMINANT,COLOBOMA OCULAR AUTOSOMAL RECESSIVE,Coloboma ocular with or without hearing impairment cleft lip/palate and/or mental retardation,Coloboma of choroid and retina,Coloboma of eye lens,Coloboma of eyelid,Coloboma of iris,Coloboma of macula,Coloboma of optic disc,COLOBOMA OF OPTIC NERVE OPTIC NERVE HEAD PITS BILATERAL CONGENITAL INCLUDED,Coloboma osteopetrosis microphthalmia macrocephaly albinism and deafness,Colobomatous macrophthalmia with microcornea syndrome,Colobomatous macrophthalmia-microcornea syndrome,Colobomatous microphthalmia,Colobomatous microphthalmia microcephaly intellectual disability and short stature,Colobomatous microphthalmia-rhizomelic dysplasia syndrome,Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome,COLORBLINDNESS PARTIAL DEUTAN SERIES,COLORBLINDNESS PARTIAL PROTAN SERIES,Colorectal Cancer,COLORECTAL CANCER HEREDITARY NONPOLYPOSIS TYPE 2,COLORECTAL CANCER HEREDITARY NONPOLYPOSIS TYPE 4,Colorectal cancer hereditary nonpolyposis type 5,COLORECTAL CANCER HEREDITARY NONPOLYPOSIS TYPE 6,COLORECTAL CANCER HEREDITARY NONPOLYPOSIS TYPE 7,COLORECTAL CANCER HEREDITARY NONPOLYPOSIS TYPE 8,COLORECTAL CANCER SUSCEPTIBILITY TO 1,COLORECTAL CANCER SUSCEPTIBILITY TO 10,Colorectal cancer susceptibility to 12,COLORECTAL CANCER SUSCEPTIBILITY TO 3,COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS,COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA,Combined deficiency of factor V and factor VIII,Combined immunodeficiency,COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA,Combined immunodeficiency due to CD27 deficiency,Combined immunodeficiency due to CD3gamma deficiency,Combined immunodeficiency due to CD70 deficiency,Combined immunodeficiency due to DOCK8 deficiency,Combined immunodeficiency due to GINS1 deficiency,Combined immunodeficiency due to IL21R deficiency,Combined immunodeficiency due to ITK deficiency,Combined immunodeficiency due to LRBA deficiency,Combined immunodeficiency due to MALT1 deficiency,Combined immunodeficiency due to Moesin deficiency,Combined immunodeficiency due to ORAI1 deficiency,Combined immunodeficiency due to OX40 deficiency,Combined immunodeficiency due to partial RAG1 deficiency,Combined immunodeficiency due to STIM1 deficiency,Combined immunodeficiency due to STK4 deficiency,Combined immunodeficiency due to TFRC deficiency,Combined immunodeficiency due to ZAP70 deficiency,Combined immunodeficiency with faciooculoskeletal anomalies,Combined immunodeficiency with granulomatosis,COMBINED IMMUNODEFICIENCY X-LINKED,Combined immunodeficiency-enteropathy spectrum,Combined malonic and methylmalonic acidemia,Combined malonic and methylmalonic aciduria,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 1,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 2,Combined oxidative phosphorylation defect type 11,Combined oxidative phosphorylation defect type 13,Combined oxidative phosphorylation defect type 14,Combined oxidative phosphorylation defect type 15,Combined oxidative phosphorylation defect type 17,Combined oxidative phosphorylation defect type 2,Combined oxidative phosphorylation defect type 20,Combined oxidative phosphorylation defect type 21,Combined oxidative phosphorylation defect type 23,Combined oxidative phosphorylation defect type 24,Combined oxidative phosphorylation defect type 25,Combined oxidative phosphorylation defect type 26,Combined oxidative phosphorylation defect type 27,Combined oxidative phosphorylation defect type 29,Combined oxidative phosphorylation defect type 30,Combined oxidative phosphorylation defect type 39,Combined oxidative phosphorylation defect type 4,Combined oxidative phosphorylation defect type 7,Combined oxidative phosphorylation defect type 8,Combined oxidative phosphorylation defect type 9,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15,Combined oxidative phosphorylation deficiency 16,Combined oxidative phosphorylation deficiency 17,Combined oxidative phosphorylation deficiency 18,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2,Combined oxidative phosphorylation deficiency 20,Combined oxidative phosphorylation deficiency 21,Combined oxidative phosphorylation deficiency 22,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23,Combined oxidative phosphorylation deficiency 24,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27,Combined oxidative phosphorylation deficiency 28,Combined oxidative phosphorylation deficiency 29,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36,Combined oxidative phosphorylation deficiency 37,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 39,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 51,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6,Combined oxidative phosphorylation deficiency 7,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9,Combined pituitary hormone deficiencies genetic forms,COMBINED SAPOSIN DEFICIENCY,Common variable immunodeficiency,COMPLEMENT COMPONENT 2 DEFICIENCY,Complement component 3 deficiency,COMPLEMENT COMPONENT 3 DEFICIENCY AUTOSOMAL RECESSIVE,COMPLEMENT COMPONENT 4 PARTIAL DEFICIENCY OF,COMPLEMENT COMPONENT 4A DEFICIENCY,COMPLEMENT COMPONENT 4B DEFICIENCY,COMPLEMENT COMPONENT 5 DEFICIENCY,COMPLEMENT COMPONENT 6 DEFICIENCY,Complement component 7 deficiency,COMPLEMENT COMPONENT 8 DEFICIENCY TYPE I,COMPLEMENT COMPONENT 8 DEFICIENCY TYPE II,COMPLEMENT COMPONENT 9 DEFICIENCY,COMPLEMENT COMPONENT C1s DEFICIENCY,COMPLEMENT FACTOR B DEFICIENCY,COMPLEMENT FACTOR D DEFICIENCY,COMPLEMENT FACTOR H DEFICIENCY,COMPLEMENT FACTOR I DEFICIENCY,COMPLEMENT HYPERACTIVATION ANGIOPATHIC THROMBOSIS AND PROTEIN-LOSING ENTEROPATHY,Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome,Complete androgen insensitivity syndrome,Complete atrioventricular septal defect with ventricular hypoplasia,Complete atrioventricular septal defect-tetralogy of Fallot,Complete cryptophthalmia,Complete hydatidiform mole,Complex craniosynostosis,Complex early-onset dystonia,Complex Hereditary Spastic Paraplegia,COMPLEX LETHAL OSTEOCHONDRODYSPLASIA,CONE DYSTROPHY 3,CONE DYSTROPHY 4,Cone dystrophy with supernormal rod response,Cone rod dystrophy,CONE-ROD DYSTROPHY 10,CONE-ROD DYSTROPHY 11,CONE-ROD DYSTROPHY 12,CONE-ROD DYSTROPHY 13,CONE-ROD DYSTROPHY 15,Cone-rod dystrophy 16,Cone-rod dystrophy 18,CONE-ROD DYSTROPHY 19,CONE-ROD DYSTROPHY 2,CONE-ROD DYSTROPHY 20,CONE-ROD DYSTROPHY 21,CONE-ROD DYSTROPHY 3,CONE-ROD DYSTROPHY 5,CONE-ROD DYSTROPHY 6,CONE-ROD DYSTROPHY 7,CONE-ROD DYSTROPHY 9,CONE-ROD DYSTROPHY AND HEARING LOSS 1,CONE-ROD DYSTROPHY AND HEARING LOSS 2,Cone-rod dystrophy X-linked 1,CONE-ROD DYSTROPHY X-LINKED 3,CONE-ROD SYNAPTIC DISORDER CONGENITAL NONPROGRESSIVE,CONE-ROD SYNAPTIC DISORDER SYNDROME CONGENITAL NONPROGRESSIVE,Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency,Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency,Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency,Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency,Congenital alpha2 antiplasmin deficiency,Congenital alveolar capillary dysplasia,Congenital amegakaryocytic thrombocytopenia,Congenital analbuminemia,CONGENITAL AND JUVENILE CATARACT,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT CAKUT1,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS ABNORMAL EARS OR DEVELOPMENTAL DELAY,CONGENITAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE,Congenital atransferrinemia,Congenital autosomal recessive small-platelet thrombocytopenia,Congenital bilateral absence of vas deferens,Congenital bile acid synthesis defect type 1,Congenital bile acid synthesis defect type 2,Congenital bile acid synthesis defect type 3,Congenital bile acid synthesis defect type 4,Congenital brain dysgenesis due to glutamine synthetase deficiency,Congenital Cataract Corneal Opacity and Developmental Glaucoma,Congenital cataract microcornea with corneal opacity,Congenital cataract-hearing loss-severe developmental delay syndrome,Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome,Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome,Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome,CONGENITAL CATARACTS FACIAL DYSMORPHISM AND NEUROPATHY,CONGENITAL CATARACTS FACIAL DYSMORPHISM AND NEUROPATHY SYNDROME,CONGENITAL CATARACTS HEARING LOSS AND NEURODEGENERATION,Congenital cataracts-facial dysmorphism-neuropathy syndrome,Congenital Cerebellar Ataxia,Congenital cerebellar ataxia due to RNU12 mutation,Congenital chloride diarrhea,Congenital chronic diarrhea with protein-losing enteropathy,congenital clubfoot,Congenital communicating hydrocephalus,Congenital contractural arachnodactyly,CONGENITAL CONTRACTURES OF THE LIMBS AND FACE HYPOTONIA AND DEVELOPMENTAL DELAY,Congenital cornea plana,Congenital deficiency in alpha-fetoprotein,Congenital diaphragmatic hernia,CONGENITAL DIARRHEAL DISORDERS,CONGENITAL DISORDER OF DEGLYCOSYLATION,Congenital Disorder of Glycosylation,Congenital disorder of glycosylation type 1G,congenital disorder of glycosylation type 1N,Congenital disorder of glycosylation type 1O,CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2A,Congenital disorder of glycosylation type 2C,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ia,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Iaa,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ib,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ic,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Icc,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Id,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ie,CONGENITAL DISORDER OF GLYCOSYLATION TYPE If,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ig,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ih,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ii,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIa,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIb,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIc,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IId,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIe,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIf,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIg,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIh,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIi,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIj,Congenital disorder of glycosylation type IIk,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIl,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIm,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIn,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIo,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIp,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIq,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIr,CONGENITAL DISORDER OF GLYCOSYLATION TYPE IIt,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ij,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ik,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Il,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Im,CONGENITAL DISORDER OF GLYCOSYLATION TYPE In,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ip,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Iq,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ir,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Is,CONGENITAL DISORDER OF GLYCOSYLATION TYPE It,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Iu,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Iw,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Ix,CONGENITAL DISORDER OF GLYCOSYLATION TYPE Iy,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION,Congenital disorder of glycosylation with defective fucosylation 1,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 2,Congenital Disorders of Glycosylation,Congenital dyserythropoietic anemia type I,Congenital dyserythropoietic anemia type II,Congenital dyserythropoietic anemia type III,Congenital dyserythropoietic anemia type IV,Congenital enteropathy due to enteropeptidase deficiency,Congenital erythropoietic porphyria,Congenital factor II deficiency,Congenital factor V deficiency,Congenital factor VII deficiency,Congenital factor X deficiency,Congenital factor XI deficiency,Congenital factor XII deficiency,Congenital factor XIII deficiency,Congenital fiber-type disproportion myopathy,Congenital fibrosis of extraocular muscles,Congenital generalized hypercontractile muscle stiffness syndrome,Congenital generalized lipodystrophy,CONGENITAL GENERALIZED LIPODYSTROPHY TYPE 3,Congenital glaucoma,CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA,Congenital heart defects and skeletal malformations,CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME,CONGENITAL HEART DEFECTS and XX sex reversal,CONGENITAL HEART DEFECTS DYSMORPHIC FACIAL FEATURES AND INTELLECTUAL DEVELOPMENTAL DISORDER,CONGENITAL HEART DEFECTS HAMARTOMAS OF TONGUE AND POLYSYNDACTYLY,CONGENITAL HEART DEFECTS MULTIPLE TYPES 2,Congenital heart defects multiple types 4,CONGENITAL HEART DEFECTS MULTIPLE TYPES 5,CONGENITAL HEART DEFECTS MULTIPLE TYPES 6,CONGENITAL HEART DEFECTS MULTIPLE TYPES 7,Congenital heart disease,CONGENITAL HEART DISEASE and NEURODEVELOPMENTAL DISORDER,CONGENITAL HEART DISEASE NONSYNDROMIC 2,Congenital Hemangioma,CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS,Congenital hereditary endothelial dystrophy type I,Congenital hereditary endothelial dystrophy type II,Congenital hereditary facial paralysis-variable hearing loss syndrome,Congenital high-molecular-weight kininogen deficiency,CONGENITAL HYPOTHYROIDISM NON-GOITROUS TYPE 2,CONGENITAL HYPOTHYROIDISM NON-GOITROUS TYPE 5,CONGENITAL HYPOTONIA EPILEPSY DEVELOPMENTAL DELAY AND DIGITAL ANOMALIES,congenital hypotonia epilepsy developmental delay digit abnormalities,congenital ichthyosis,Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome,congenital inability to experience pain,Congenital insensitivity to pain with anhidrosis,Congenital insensitivity to pain with severe intellectual disability,Congenital intrauterine infection-like syndrome,Congenital intrinsic factor deficiency,Congenital isolated ACTH deficiency,Congenital lactase deficiency,Congenital lactic acidosis Saguenay-Lac-Saint-Jean type,Congenital lethal myopathy Compton-North type,Congenital limbs-face contractures-hypotonia-developmental delay syndrome,Congenital lipomatous overgrowth vascular malformations and epidermal nevi,Congenital Lower Urinary Tract Obstruction,Congenital lymphatic dysplasia with hydrops and/or lymphoedema,Congenital megabladder,Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization,Congenital mesoblastic nephroma,Congenital Microcephaly Epileptic Encephalopathy Blindness and Failure to Thrive,Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome,Congenital multicore myopathy with external ophthalmoplegia,Congenital Muscular Dystrophy,Congenital muscular dystrophy due to LMNA mutation,Congenital muscular dystrophy Fukuyama type,Congenital muscular dystrophy Ullrich type,Congenital muscular dystrophy with cerebellar involvement,Congenital muscular dystrophy with integrin alpha-7 deficiency,Congenital muscular dystrophy with intellectual disability,Congenital muscular dystrophy with intellectual disability and severe epilepsy,Congenital muscular dystrophy without intellectual disability,Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome,Congenital Myasthenic Syndrome Type 19,Congenital Myasthenic Syndrome with Episodic Apnea,Congenital myasthenic syndromes with glycosylation defect,Congenital myopathy Paradas type,CONGENITAL MYOPATHY WITH EXCESS OF MUSCLE SPINDLES,Congenital myopathy with excess of thin filaments,Congenital myopathy with internal nuclei and atypical cores,Congenital myopathy with myasthenic-like onset,Congenital Myopathy with Prominent Internal Nuclei and Atypical Cores,Congenital myopathy with reduced type 2 muscle fibers,Congenital nephrotic syndrome Finnish type,Congenital neutropenia-myelofibrosis-nephromegaly syndrome,Congenital non-bullous ichthyosiform erythroderma,Congenital non-communicating hydrocephalus,Congenital or early infantile CACH syndrome,Congenital plasminogen activator inhibitor type 1 deficiency,Congenital prekallikrein deficiency,Congenital primary aphakia,Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome,Congenital ptosis,Congenital reticular ichthyosiform erythroderma,Congenital short bowel syndrome,Congenital sialidosis type 2,Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome,Congenital sodium diarrhea,Congenital stationary night blindness,Congenital Stromal Corneal Dystrophy,Congenital sucrase-isomaltase deficiency,CONGENITAL SYSTEMIC GLUTAMINE DEFICIENCY,Congenital thrombotic thrombocytopenic purpura,Congenital tufting enteropathy,CONGENITAL VARIANT OF RETT SYNDROME,Congenital vascular tumours,Congenital vertebral-cardiac-renal anomalies syndrome,Congenital vertical talus bilateral,Congenital vertical talus unilateral,Congenitally uncorrected transposition of the great arteries,Congenitally uncorrected transposition of the great arteries with cardiac malformation,Congenitally uncorrected transposition of the great arteries with coarctation,Connective tissue disorder due to lysyl hydroxylase-3 deficiency,Conotruncal heart malformations,Constitutional megaloblastic anemia with severe neurologic disease,Constitutional mismatch repair deficiency syndrome,Continuous spikes and waves during sleep,CONTRACTURAL ARACHNODACTYLY CONGENITAL,CONTRACTURES PTERYGIA AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1A,CONTRACTURES PTERYGIA AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1B,CONVULSIONS FAMILIAL INFANTILE WITH PAROXYSMAL CHOREOATHETOSIS,COPB1-related severe intellectual disability syndrome with cataracts and variable microcephaly,COPROPORPHYRIA HEREDITARY,Coralliform cataract,CORNEA PLANA 2 AUTOSOMAL RECESSIVE,CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS,CORNEAL DYSTROPHY AVELLINO TYPE,CORNEAL DYSTROPHY CONGENITAL STROMAL,CORNEAL DYSTROPHY EPITHELIAL BASEMENT MEMBRANE,CORNEAL DYSTROPHY FLECK,CORNEAL DYSTROPHY FUCHS ENDOTHELIAL 1,CORNEAL DYSTROPHY FUCHS ENDOTHELIAL 3,Corneal dystrophy fuchs endothelial 4,CORNEAL DYSTROPHY FUCHS ENDOTHELIAL 6,Corneal dystrophy fuchs endothelial 8,CORNEAL DYSTROPHY FUCHS ENDOTHELIAL TYPE 6,CORNEAL DYSTROPHY GELATINOUS DROP-LIKE,CORNEAL DYSTROPHY GROENOUW TYPE I,CORNEAL DYSTROPHY LATTICE TYPE I,CORNEAL DYSTROPHY LATTICE TYPE IIIA,CORNEAL DYSTROPHY MEESMANN 1,CORNEAL DYSTROPHY MEESMANN 2,CORNEAL DYSTROPHY POSTERIOR POLYMORPHOUS 1,CORNEAL DYSTROPHY POSTERIOR POLYMORPHOUS 2,CORNEAL DYSTROPHY POSTERIOR POLYMORPHOUS 3,CORNEAL DYSTROPHY POSTERIOR POLYMORPHOUS 4,CORNEAL DYSTROPHY REIS-BUCKLERS TYPE,CORNEAL DYSTROPHY THIEL-BEHNKE TYPE,Corneal dystrophy-perceptive deafness syndrome,Corneal endothelial dystrophy,Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome,Cornelia de Lange syndrome,CORNELIA DE LANGE SYNDROME 1,CORNELIA DE LANGE SYNDROME 2,CORNELIA DE LANGE SYNDROME 3 WITH OR WITHOUT MIDLINE BRAIN DEFECTS,CORNELIA DE LANGE SYNDROME 4 WITH OR WITHOUT MIDLINE BRAIN DEFECTS,CORNELIA DE LANGE SYNDROME 5,Cornelia de Lange Syndrome HDAC8 X-linked dominant,CORNELIA DE LANGE SYNDROME TYPE 1,CORNELIA DE LANGE SYNDROME TYPE 2,CORNELIA DE LANGE SYNDROME TYPE 3,Cornelia de Lange-like syndrome,CORNELIA DE LANGE-LIKE SYNDROME HDAC8 XLR,Coronal Craniosynostosis,CORONARY ARTERY DISEASE AUTOSOMAL DOMINANT 1,Coronary Artery Disease Autosomal Dominant 2,Coronary Heart Disease Susceptibility To 1,Coronary Heart Disease Susceptibility To 6,CORONARY HEART DISEASE SUSCEPTIBILITY TO 7,CORPUS CALLOSUM AGENESIS OF WITH ABNORMAL GENITALIA,CORPUS CALLOSUM AGENESIS OF WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA,CORPUS CALLOSUM AGENESIS OF WITH MENTAL RETARDATION OCULAR COLOBOMA AND MICROGNATHIA,Corpus callosum agenesis-abnormal genitalia syndrome,Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome,Corpus callosum agenesis-neuronopathy syndrome,CORPUS CALLOSUM PARTIAL AGENESIS OF X-LINKED,Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 1,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 10,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 2,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 3,Cortical dysplasia complex with other brain malformations 4,Cortical dysplasia complex with other brain malformations 5,Cortical dysplasia complex with other brain malformations 6,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 7,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 8,CORTICAL DYSPLASIA COMPLEX WITH OTHER BRAIN MALFORMATIONS 9,Cortical dysplasia-focal epilepsy syndrome,CORTICAL MALFORMATIONS OCCIPITAL,CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY,CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY,CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY,CORTISONE REDUCTASE DEFICIENCY 1,Cortisone reductase deficiency 2,COSTELLO SYNDROME,COUMARIN RESISTANCE,COUSIN SYNDROME,Cousin Syndrome; Craniofacial Dysmorphism Hypoplasia of Scapula and Pelvis and Short Stature,COWDEN SYNDROME,COWDEN SYNDROME 1,COWDEN SYNDROME 4,COWDEN SYNDROME 5,COWDEN SYNDROME 6,COWDEN SYNDROME 7,COX15-related Leigh Syndrome,COX16-related Developmental Disorder,Coxopodopatellar syndrome,Cranio-cervical dystonia with laryngeal and upper-limb involvement,Craniodiaphyseal dysplasia,CRANIODIAPHYSEAL DYSPLASIA AUTOSOMAL DOMINANT,Cranioectodermal dysplasia,CRANIOECTODERMAL DYSPLASIA 1,Cranioectodermal dysplasia 2,CRANIOECTODERMAL DYSPLASIA 3,Cranioectodermal dysplasia 4,CRANIOECTODERMAL DYSPLASIA TYPE 3,CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME,Craniofacial anomalies corpus callosum dysgenesis ptosis and developmental delay,Craniofacial dysmorphism skeletal anomalies and mental retardation syndrome,Craniofacial dysplasia-osteopenia syndrome,Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome,Craniofacial Neurological Cardiovascular and Skeletal Features,Craniofacial with neurodevelopment disorders,CRANIOFACIAL-DEAFNESS-HAND SYNDROME,Craniofrontonasal dysplasia,CRANIOFRONTONASAL SYNDROME,CRANIOLENTICULOSUTURAL DYSPLASIA,Craniometaphyseal dysplasia,CRANIOMETAPHYSEAL DYSPLASIA AUTOSOMAL DOMINANT,CRANIOMETAPHYSEAL DYSPLASIA AUTOSOMAL RECESSIVE,CRANIOMETAPHYSEAL DYSPLASIA JACKSON TYPE,CRANIOOSTEOARTHROPATHY,Craniopharyngioma,Craniorachischisis,CRANIOSYNOSTOSIS 1,CRANIOSYNOSTOSIS 2,Craniosynostosis 3,CRANIOSYNOSTOSIS 4,Craniosynostosis 5 susceptibility to,CRANIOSYNOSTOSIS 6,Craniosynostosis 7,Craniosynostosis and dental anomalies,Craniosynostosis Boston type,CRANIOSYNOSTOSIS TYPE 2,Craniosynostosis-dental anomalies,Craniosynostosis-microretrognathia-severe intellectual disability syndrome,CRB1-related Leber Congenital Amaurosis and Retinitis Pigmentosa,CREATINE PHOSPHOKINASE ELEVATED SERUM,Cree leukoencephalopathy,CREUTZFELDT-JAKOB DISEASE,Crigler-Najjar syndrome type 1,Crigler-Najjar syndrome type 2,CRIGLER-NAJJAR SYNDROME TYPE I,CRIGLER-NAJJAR SYNDROME TYPE II,CRISPONI SYNDROME,Crisponi/CISS1-like phenotype associated with early-onset retinitis pigmentosa,CRISPONI/COLD-INDUCED SWEATING SYNDROME 1,CRISPONI/COLD-INDUCED SWEATING SYNDROME 2,Crouzon disease,CROUZON SYNDROME,CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS,Crouzon syndrome-acanthosis nigricans syndrome,CRX-Related Leber Congenital Amaurosis Leber congenital amaurosis 7,CRYOHYDROCYTOSIS,Cryptogenic multifocal ulcerous stenosing enteritis,Cryptophthalmos unilateral or bilateral isolated,Cryptorchidism unilateral or bilateral,CSNK2A1 syndrome,CSNK2B-related developmental disorder monoallelic,CTBP1-related developmental disorder monoallelic,CTCF-related neurodevelopmental disorder,CTNND2-related neurodevelopmental disorder,CUL3-related developmental disorder monoallelic,CULLER-JONES SYNDROME,CURRARINO SYNDROME,Curry-Jones Syndrome,Cushing disease,Cushing syndrome due to macronodular adrenal hyperplasia,Cutaneous mastocytoma,CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME FAMILIAL,Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome,CUTIS LAXA AUTOSOMAL DOMINANT 1,CUTIS LAXA AUTOSOMAL DOMINANT 2,Cutis laxa autosomal dominant 3,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IA,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IB,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IC,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IIA,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IIB,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IIC,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IID,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IIIA,CUTIS LAXA AUTOSOMAL RECESSIVE TYPE IIIB,Cutis laxa with severe pulmonary gastrointestinal and urinary anomalies,Cutis marmorata telangiectatica congenita,CYANOSIS TRANSIENT NEONATAL,CYCLIC NEUTROPENIA,CYLINDROMATOSIS FAMILIAL,Cystathionine beta-synthase deficiency,CYSTATHIONINURIA,Cystic Fibrosis,Cystic leukoencephalopathy without megalencephaly,CYSTINOSIS ADULT NONNEPHROPATHIC,CYSTINOSIS LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE,CYSTINOSIS NEPHROPATHIC,CYSTINOSIS NEPHROPATHIC TYPE,CYSTINURIA,Cystinuria type A,Cystinuria type B,CYTOCHROME P450 SUBFAMILY I POLYPEPTIDE 2,CYTOCHROME P450 SUBFAMILY IIA POLYPEPTIDE 6,Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder,CZECH DYSPLASIA,D-2-hydroxyglutaric aciduria,D-2-hydroxyglutaric aciduria 1,D-2-hydroxyglutaric aciduria 2,D-BIFUNCTIONAL PROTEIN DEFICIENCY,D-GLYCERIC ACIDURIA,D-LACTIC ACIDURIA WITH GOUT,Danon disease,DARIER DISEASE,DARIER-WHITE DISEASE,DDB1-associated neurodevelopmental syndrome,DDOST-CDG,DDX23-related developmental disorder monoallelic,DDX41-related hematologic malignancy predisposition syndrome,De novo thrombotic microangiopathy after kidney transplantation,De Sanctis-Cacchione syndrome,Deafness aminoglycoside-induced,DEAFNESS AND MYOPIA,DEAFNESS AUTOSOMAL DOMINANT 1 WITH OR WITHOUT THROMBOCYTOPENIA,DEAFNESS AUTOSOMAL DOMINANT 10,DEAFNESS AUTOSOMAL DOMINANT 11,DEAFNESS AUTOSOMAL DOMINANT 12,DEAFNESS AUTOSOMAL DOMINANT 13,DEAFNESS AUTOSOMAL DOMINANT 15,DEAFNESS AUTOSOMAL DOMINANT 17,DEAFNESS AUTOSOMAL DOMINANT 20,DEAFNESS AUTOSOMAL DOMINANT 22,DEAFNESS AUTOSOMAL DOMINANT 23,DEAFNESS AUTOSOMAL DOMINANT 25,DEAFNESS AUTOSOMAL DOMINANT 27,DEAFNESS AUTOSOMAL DOMINANT 28,DEAFNESS AUTOSOMAL DOMINANT 2A,DEAFNESS AUTOSOMAL DOMINANT 2B,DEAFNESS AUTOSOMAL DOMINANT 34 WITH OR WITHOUT INFLAMMATION,DEAFNESS AUTOSOMAL DOMINANT 36,DEAFNESS AUTOSOMAL DOMINANT 37,DEAFNESS AUTOSOMAL DOMINANT 39 WITH DENTINOGENESIS IMPERFECTA 1,DEAFNESS AUTOSOMAL DOMINANT 3A,DEAFNESS AUTOSOMAL DOMINANT 3B,DEAFNESS AUTOSOMAL DOMINANT 40,DEAFNESS AUTOSOMAL DOMINANT 41,DEAFNESS AUTOSOMAL DOMINANT 44,DEAFNESS AUTOSOMAL DOMINANT 4A,DEAFNESS AUTOSOMAL DOMINANT 4B,Deafness autosomal dominant 5,Deafness autosomal dominant 50,DEAFNESS AUTOSOMAL DOMINANT 56,DEAFNESS AUTOSOMAL DOMINANT 6,DEAFNESS AUTOSOMAL DOMINANT 64,DEAFNESS AUTOSOMAL DOMINANT 65,DEAFNESS AUTOSOMAL DOMINANT 66,DEAFNESS AUTOSOMAL DOMINANT 67,Deafness autosomal dominant 68,DEAFNESS AUTOSOMAL DOMINANT 69,DEAFNESS AUTOSOMAL DOMINANT 7,DEAFNESS AUTOSOMAL DOMINANT 70,DEAFNESS AUTOSOMAL DOMINANT 71,DEAFNESS AUTOSOMAL DOMINANT 72,DEAFNESS AUTOSOMAL DOMINANT 73,DEAFNESS AUTOSOMAL DOMINANT 74,DEAFNESS AUTOSOMAL DOMINANT 75,DEAFNESS AUTOSOMAL DOMINANT 76,DEAFNESS AUTOSOMAL DOMINANT 77,DEAFNESS AUTOSOMAL DOMINANT 78,DEAFNESS AUTOSOMAL DOMINANT 79,DEAFNESS AUTOSOMAL DOMINANT 9,DEAFNESS AUTOSOMAL DOMINANT TYPE 13,deafness autosomal dominant type 2B,DEAFNESS AUTOSOMAL DOMINANT TYPE 39 WITH DENTINOGENESIS IMPERFECTA 1,DEAFNESS AUTOSOMAL RECESSIVE,DEAFNESS AUTOSOMAL RECESSIVE 100,Deafness autosomal recessive 101,Deafness autosomal recessive 102,DEAFNESS AUTOSOMAL RECESSIVE 103,Deafness autosomal recessive 104,DEAFNESS AUTOSOMAL RECESSIVE 106,DEAFNESS AUTOSOMAL RECESSIVE 107,DEAFNESS AUTOSOMAL RECESSIVE 108,DEAFNESS AUTOSOMAL RECESSIVE 109,DEAFNESS AUTOSOMAL RECESSIVE 110,DEAFNESS AUTOSOMAL RECESSIVE 111,DEAFNESS AUTOSOMAL RECESSIVE 112,DEAFNESS AUTOSOMAL RECESSIVE 113,DEAFNESS AUTOSOMAL RECESSIVE 114,DEAFNESS AUTOSOMAL RECESSIVE 115,DEAFNESS AUTOSOMAL RECESSIVE 116,DEAFNESS AUTOSOMAL RECESSIVE 117,DEAFNESS AUTOSOMAL RECESSIVE 12,DEAFNESS AUTOSOMAL RECESSIVE 15,DEAFNESS AUTOSOMAL RECESSIVE 16,DEAFNESS AUTOSOMAL RECESSIVE 18A,DEAFNESS AUTOSOMAL RECESSIVE 18B,DEAFNESS AUTOSOMAL RECESSIVE 1A,DEAFNESS AUTOSOMAL RECESSIVE 1B,DEAFNESS AUTOSOMAL RECESSIVE 2,DEAFNESS AUTOSOMAL RECESSIVE 21,DEAFNESS AUTOSOMAL RECESSIVE 22,DEAFNESS AUTOSOMAL RECESSIVE 23,Deafness autosomal recessive 24,DEAFNESS AUTOSOMAL RECESSIVE 25,DEAFNESS AUTOSOMAL RECESSIVE 26,DEAFNESS AUTOSOMAL RECESSIVE 26 MODIFIER OF,DEAFNESS AUTOSOMAL RECESSIVE 28,DEAFNESS AUTOSOMAL RECESSIVE 29,DEAFNESS AUTOSOMAL RECESSIVE 3,DEAFNESS AUTOSOMAL RECESSIVE 30,DEAFNESS AUTOSOMAL RECESSIVE 31,DEAFNESS AUTOSOMAL RECESSIVE 32 WITH OR WITHOUT IMMOTILE SPERM,DEAFNESS AUTOSOMAL RECESSIVE 35,DEAFNESS AUTOSOMAL RECESSIVE 36 WITH OR WITHOUT VESTIBULAR INVOLVEMENT,DEAFNESS AUTOSOMAL RECESSIVE 37,DEAFNESS AUTOSOMAL RECESSIVE 39,DEAFNESS AUTOSOMAL RECESSIVE 4 WITH ENLARGED VESTIBULAR AQUEDUCT,Deafness autosomal recessive 42,Deafness autosomal recessive 44,DEAFNESS AUTOSOMAL RECESSIVE 48,DEAFNESS AUTOSOMAL RECESSIVE 49,DEAFNESS AUTOSOMAL RECESSIVE 53,DEAFNESS AUTOSOMAL RECESSIVE 57,DEAFNESS AUTOSOMAL RECESSIVE 59,DEAFNESS AUTOSOMAL RECESSIVE 6,DEAFNESS AUTOSOMAL RECESSIVE 61,DEAFNESS AUTOSOMAL RECESSIVE 63,Deafness autosomal recessive 66,DEAFNESS AUTOSOMAL RECESSIVE 67,Deafness autosomal recessive 68,DEAFNESS AUTOSOMAL RECESSIVE 7,DEAFNESS AUTOSOMAL RECESSIVE 70,DEAFNESS AUTOSOMAL RECESSIVE 74,DEAFNESS AUTOSOMAL RECESSIVE 76,DEAFNESS AUTOSOMAL RECESSIVE 77,Deafness autosomal recessive 79,Deafness autosomal recessive 8,DEAFNESS AUTOSOMAL RECESSIVE 84A,DEAFNESS AUTOSOMAL RECESSIVE 84B,DEAFNESS AUTOSOMAL RECESSIVE 86,DEAFNESS AUTOSOMAL RECESSIVE 88,DEAFNESS AUTOSOMAL RECESSIVE 89,DEAFNESS AUTOSOMAL RECESSIVE 9,Deafness autosomal recessive 91,DEAFNESS AUTOSOMAL RECESSIVE 93,DEAFNESS AUTOSOMAL RECESSIVE 94,DEAFNESS AUTOSOMAL RECESSIVE 97,DEAFNESS AUTOSOMAL RECESSIVE 98,DEAFNESS AUTOSOMAL RECESSIVE 99,deafness autosomal recessive type 12,deafness autosomal recessive type 2,DEAFNESS AUTOSOMAL RECESSIVE TYPE 53,DEAFNESS CONGENITAL AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY,DEAFNESS CONGENITAL HEART DEFECTS AND POSTERIOR EMBRYOTOXON,DEAFNESS CONGENITAL WITH INNER EAR AGENESIS MICROTIA AND MICRODONTIA,DEAFNESS CONGENITAL WITH ONYCHODYSTROPHY AUTOSOMAL DOMINANT,Deafness Dystonia and Central Hypomyelination with Disorganization of the Golgi Apparatus,DEAFNESS DYSTONIA AND CEREBRAL HYPOMYELINATION,Deafness nonsyndromic sensorineural mitochondrial,DEAFNESS ONYCHODYSTROPHY OSTEODYSTROPHY MENTAL RETARDATION AND SEIZURES SYNDROME,Deafness with Labyrinthine Aplasia Microtia and Microdontia,DEAFNESS X-LINKED 1,DEAFNESS X-LINKED 2,DEAFNESS X-LINKED 4,DEAFNESS X-LINKED 5 WITH PERIPHERAL NEUROPATHY,DEAFNESS X-LINKED 6,DEAFNESS X-LINKED 7,DEAFNESS X-LINKED TYPE 1,Deafness Y-linked 2,Deafness-enamel hypoplasia-nail defects syndrome,Deafness-encephaloneuropathy-obesity-valvulopathy syndrome,Deafness-infertility syndrome,Deafness-lymphedema-leukemia syndrome,Dedifferentiated liposarcoma,DEEAH SYNDROME,Defect in Cholesterol Biosynthesis,Defects in Neuronal Migration and Axon Guidance,Deficiency in anterior pituitary function-variable immunodeficiency syndrome,Dehydrated hereditary stomatocytosis,Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema,Dehydrated hereditary stomatocytosis 2,Dejerine-Sottas syndrome,DELAYED SLEEP PHASE DISORDER SUSCEPTIBILITY TO,Deletion 5q35,DELPIRE-MCNEILL SYNDROME,Delta-beta thalassemia,Delta-sarcoglycan-related  limb-girdle muscular dystrophy R6,DEMENTIA LEWY BODY,DEND syndrome,DENGUE VIRUS SUSCEPTIBILITY TO DENGUE FEVER SUSCEPTIBILITY TO INCLUDED,Dense deposit disease,Dent disease 1,DENT DISEASE 2,Dent disease type 1,Dent disease type 2,DENTAL ANOMALIES AND SHORT STATURE,Dentatorubral pallidoluysian atrophy,DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY,Dentin dysplasia type I,Dentin dysplasia type I with microdontia and misshapen teeth,DENTIN DYSPLASIA TYPE II,DENTINOGENESIS IMPERFECTA 1,DENTINOGENESIS IMPERFECTA SHIELDS TYPE II,DENTINOGENESIS IMPERFECTA SHIELDS TYPE III,Dentinogenesis imperfecta type 2,Dentinogenesis imperfecta type 3,DENYS-DRASH SYNDROME,Dermatitis atopic 2,DERMATOFIBROSARCOMA PROTUBERANS,DERMATOPATHIA PIGMENTOSA RETICULARIS,Dermatosparaxis Ehlers-Danlos syndrome,Desanto-shinawi syndrome,DESBUQUOIS DYSPLASIA 1,DESBUQUOIS DYSPLASIA 2,Desbuquois syndrome,Desmin-related myopathy with Mallory body-like inclusions,Desminopathy,DESMOID DISEASE HEREDITARY,Desmoid tumor,Desmoplastic small round cell tumor,Desmoplastic/nodular medulloblastoma,DESMOSTEROLOSIS,Developmental and Epileptic Encephalopathy,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 1,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 11,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 12,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 14,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 15,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 16,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 17,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 19,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 21,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 24,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 25 WITH AMELOGENESIS IMPERFECTA,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 26,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 27,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 29,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 3,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 30,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 32,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 34,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 35,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 36,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 39,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 40,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 41,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 42,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 43,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 44,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 45,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 46,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 47,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 48,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 49,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 5,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 50,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 51,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 53,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 55,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 56,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 57,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 58,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 59,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 60,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 62,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 63,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 64,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 67,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 68,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 69,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 71,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 72,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 73,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 74,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 75,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 78,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 79,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 8,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 81,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 85 WITH OR WITHOUT MIDLINE BRAIN DEFECTS,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 86,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 9,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 90,Developmental and epileptic encephalopathy 91,Developmental and epileptic encephalopathy 92,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 93,Developmental and expressive language delay,Developmental and infantile epileptic encephalopathy,Developmental and speech delay due to SOX5 deficiency,Developmental and Speech Delay Postnatal Microcephaly and Dysmorphic Features,Developmental delay and distinctive facial features,DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES,Developmental Delay Congenital Anomalies and Dysmorphic Features,Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency,Developmental Delay Epilepsy Cerebellar Atrophy and Osteopenia,Developmental delay happy demeanor distinctive facial features and congenital anomalies,Developmental delay hypotonia and autistic features,Developmental delay ID obesity and dysmorphic features,DEVELOPMENTAL DELAY IMPAIRED GROWTH DYSMORPHIC FACIES AND AXONAL NEUROPATHY,Developmental delay macrocephaly and dysmorphic features,Developmental delay with autism spectrum disorder and gait instability,DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES,DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM,DEVELOPMENTAL DELAY WITH SHORT STATURE DYSMORPHIC FACIAL FEATURESAND SPARSE HAIR,DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES,Developmental delay-facial dysmorphism syndrome due to MED13L deficiency,Developmental Disorder with Microcephaly and Congenital Arthrogryposis,Developmental Disorders with Diverse Phenotypes,Developmental epileptic encephalopathy,Developmental malformations-deafness-dystonia syndrome,DHRS3 related craniosynostosis,DIABETES INSIPIDUS NEPHROGENIC AUTOSOMAL,Diabetes insipidus nephrogenic X-linked,DIABETES INSIPIDUS NEUROHYPOPHYSEAL,Diabetes Mellitus 6q24-Related Transient Neonatal,DIABETES MELLITUS INSULIN-RESISTANT WITH ACANTHOSIS NIGRICANS,Diabetes Mellitus KCNJ11-Related Transient Neonatal,DIABETES MELLITUS KETOSIS-PRONE,DIABETES MELLITUS NEONATAL WITH CONGENITAL HYPOTHYROIDISM,DIABETES MELLITUS PERMANENT NEONATAL 1,DIABETES MELLITUS PERMANENT NEONATAL 2,DIABETES MELLITUS PERMANENT NEONATAL 3,DIABETES MELLITUS PERMANENT NEONATAL 4,Diabetes Mellitus Permanent Neonatal with Cerebellar Agenesis,DIABETES MELLITUS TRANSIENT NEONATAL 1,DIABETES MELLITUS TRANSIENT NEONATAL 2,DIABETES MELLITUS TRANSIENT NEONATAL 3,DIAMOND-BLACKFAN ANEMIA 1,DIAMOND-BLACKFAN ANEMIA 10,DIAMOND-BLACKFAN ANEMIA 11,DIAMOND-BLACKFAN ANEMIA 12,Diamond-Blackfan anemia 13,DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS,DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS,Diamond-Blackfan anemia 16,DIAMOND-BLACKFAN ANEMIA 17,DIAMOND-BLACKFAN ANEMIA 18,DIAMOND-BLACKFAN ANEMIA 19,DIAMOND-BLACKFAN ANEMIA 20,DIAMOND-BLACKFAN ANEMIA 3,DIAMOND-BLACKFAN ANEMIA 4,DIAMOND-BLACKFAN ANEMIA 5,DIAMOND-BLACKFAN ANEMIA 6,DIAMOND-BLACKFAN ANEMIA 7,DIAMOND-BLACKFAN ANEMIA 8,DIAMOND-BLACKFAN ANEMIA 9,Diamond-Blackfan anemia with cleft palate and abnormal thumbs,DIAMOND-BLACKFAN ANEMIA-LIKE,DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome,Diaphanospondylodysostosis,DIAPHRAGMATIC HERNIA 3,Diaphragmatic hernia-short bowel-asplenia syndrome,Diaphyseal medullary stenosis with malignant fibrous histiocytoma,Diaphyseal medullary stenosis-bone malignancy syndrome,DIARRHEA 1 SECRETORY CHLORIDE CONGENITAL,DIARRHEA 10 PROTEIN-LOSING ENTEROPATHY TYPE,DIARRHEA 11 MALABSORPTIVE CONGENITAL,DIARRHEA 2 WITH MICROVILLUS ATROPHY,DIARRHEA 3 SECRETORY SODIUM CONGENITAL WITH OR WITHOUT OTHER CONGENITAL ANOMALIES,DIARRHEA 4 MALABSORPTIVE CONGENITAL,DIARRHEA 5 WITH TUFTING ENTEROPATHY CONGENITAL,DIARRHEA 6,DIARRHEA 7 PROTEIN-LOSING ENTEROPATHY TYPE,DIARRHEA 8 SECRETORY SODIUM CONGENITAL,DIARRHEA 9,Diastrophic dwarfism,Diastrophic dysplasia,Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency,Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency,Dicarboxylic aminoaciduria,Diencephalic-mesencephalic junction dysplasia,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 1,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 2,Dienoyl-CoA reductase deficiency with hyperlysinemia,DIETS-JONGMANS SYNDROME,Differentiated thyroid carcinoma,Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome,Diffuse cutaneous systemic sclerosis,Diffuse palmoplantar keratoderma with painful fissures,Diffuse panbronchiolitis,DIGEORGE SYNDROME,DIGITAL ARTHROPATHY-BRACHYDACTYLY FAMILIAL,DIGITAL CLUBBING ISOLATED CONGENITAL,Dihydrolipoamide Dehydrogenase (E3) Deficiency,DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY,Dihydropteridine reductase deficiency,DIHYDROPYRIMIDINASE DEFICIENCY,DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY,Dihydropyrimidinuria,Dilated cardiomyopathy with ataxia,Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY,Disorder of Golgi homeostasis,Disordered cortical neuronal migration,DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY,Disseminated superficial actinic porokeratosis,Distal 16p11.2 microdeletion syndrome,Distal 17p13.3 microdeletion syndrome,Distal 22q11.2 microdeletion syndrome,Distal anoctaminopathy,DISTAL ARTHROGRYPOSIS TYPE,Distal arthrogryposis type 1,DISTAL ARTHROGRYPOSIS TYPE 2A,Distal arthrogryposis type 5D,Distal hereditary motor neuropathy Jerash type,Distal hereditary motor neuropathy type 2,Distal hereditary motor neuropathy type 5,Distal hereditary motor neuropathy type 7,Distal monosomy 12p,Distal monosomy 15q,Distal monosomy 1q,Distal myopathy Tateyama type,Distal myopathy Welander type,Distal myopathy with anterior tibial onset,Distal myopathy with posterior leg and anterior hand involvement,Distal myotilinopathy,Distal nebulin myopathy,Distal renal tubular acidosis with anemia,distal renal tubular acidosis with deafness,DISTINCT DNA BREAKAGE SYNDROME,DITRA,DK1-CDG,DKC1-Related Dyskeratosis Congenita,DL-2-hydroxyglutaric aciduria,DLG4 related intellectual disability,DLG5-associated developmental disorder biallelic,DLG5-associated developmental disorder monoallelic,DNA Repair-Proficient Trichothiodystrophy,DNA2-related mitochondrial DNA deletion syndrome,DNAJB2-related Charcot-Marie-Tooth disease type 2,DNAJB6-related  limb-girdle muscular dystrophy D1,DNM1L-related developmental disorder monoallelic,DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect,DOCK2 deficiency,Dominant beta-thalassemia,Dominant hypophosphatemia with nephrolithiasis or osteoporosis,DONNAI-BARROW SYNDROME,DONOHUE SYNDROME,DOORS syndrome,Dopa-Responsive Dystonia,Dopa-responsive dystonia due to sepiapterin reductase deficiency,DOPAMINE BETA-HYDROXYLASE DEFICIENCY,DOWLING-DEGOS DISEASE,DOWLING-DEGOS DISEASE 1,Dowling-Degos disease 2,DOWLING-DEGOS DISEASE 4,DOWN SYNDROME,DOYNE HONEYCOMB RETINAL DYSTROPHY,DPAGT1-CDG,DPM1-CDG,DPM3-CDG,DPYSL5-related developmental disorder monoallelic,DRAVET SYNDROME,DRUG METABOLISM ALTERED CES1-RELATEDCARBOXYLESTERASE 1 DEFICIENCY INCLUDED,DRUG METABOLISM ALTERED CYP2C8-RELATED,DRUG METABOLISM POOR CYP2C19-RELATEDMEPHENYTOIN POOR METABOLISM OF INCLUDED,DRUG METABOLISM POOR CYP2D6-RELATED DRUG METABOLISM ULTRARAPID CYP2D6-RELATED INCLUDED,Drug- or toxin-induced pulmonary arterial hypertension,DSP-related developmental disorder,Du Pan syndrome,Duane retraction syndrome,DUANE RETRACTION SYNDROME 2,DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS,Duane retraction syndrome with congenital deafness,Duane Syndrome Aberrant Extraocular Muscle Innervation and Inner-Ear Defects,DUANE-RADIAL RAY SYNDROME,DUBIN-JOHNSON SYNDROME,Dubowitz syndrome,Duchenne Muscular Dystrophy,DYGGVE-MELCHIOR-CLAUSEN DISEASE,DYGGVE-MELCHIOR-CLAUSEN SYNDROME/SMITH-MCCORT DYSPLASIA,DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion,Dysbetalipoproteinemia,DYSCHROMATOSIS SYMMETRICA HEREDITARIA,DYSCHROMATOSIS SYMMETRICA HEREDITARIA 1,Dyschromatosis universalis hereditaria,DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1,Dyschromatosis universalis hereditaria 3,Dysequilibrium syndrome,Dysferlin-related  limb-girdle muscular dystrophy R2,DYSFIBRINOGENEMIA CONGENITALHYPODYSFIBRINOGENEMIA CONGENITAL INCLUDED,Dyskeratosis congenita,DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 1,DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 2,DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 3,DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 4,DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 6,DYSKERATOSIS CONGENITA AUTOSOMAL RECESSIVE 1,Dyskeratosis congenita autosomal recessive 2,DYSKERATOSIS CONGENITA AUTOSOMAL RECESSIVE 3,DYSKERATOSIS CONGENITA AUTOSOMAL RECESSIVE 4,DYSKERATOSIS CONGENITA AUTOSOMAL RECESSIVE 5,DYSKERATOSIS CONGENITA AUTOSOMAL RECESSIVE 6,DYSKERATOSIS CONGENITA X-LINKED,DYSKINESIA FAMILIAL WITH FACIAL MYOKYMIA,DYSKINESIA LIMB AND OROFACIAL INFANTILE-ONSET,DYSLEXIA SUSCEPTIBILITY TO 1,Dysmorphic Features Intellectual Disability and Neurological Manifestations,Dysosteosclerosis,Dyssegmental dysplasia Silverman-Handmaker type,Dysspondyloenchondromatosis,DYSTONIA 1 TORSION AUTOSOMAL DOMINANT,DYSTONIA 11 MYOCLONIC,DYSTONIA 12,DYSTONIA 16,DYSTONIA 2 TORSION AUTOSOMAL RECESSIVE,DYSTONIA 24,DYSTONIA 25,DYSTONIA 26 MYOCLONIC,DYSTONIA 27,DYSTONIA 28 CHILDHOOD-ONSET,DYSTONIA 3 TORSION X-LINKED,DYSTONIA 4 TORSION AUTOSOMAL DOMINANT,DYSTONIA 6 TORSION,DYSTONIA 9,Dystonia childhood-onset with optic atrophy and basal ganglia abnormalities,DYSTONIA DOPA-RESPONSIVE,DYSTONIA DOPA-RESPONSIVE DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY,DYSTONIA JUVENILE-ONSET,DYSTONIA TYPE 5,Dystonia-parkinsonism-hypermanganesemia syndrome,DYSTROPHIA MYOTONICA TYPE 1,Dystrophic epidermolysis bullosa pruriginosa,Ear-patella-short stature syndrome,Early infantile epileptic encephalopathy,EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY AND MICROCEPHALY,Early myoclonic encephalopathy,Early onset epileptic encephalopathy,Early Onset Isolated Mitochondrial Complex I Deficiency,Early-onset anterior polar cataract,Early-onset autosomal dominant Alzheimer disease,Early-onset calcifying leukoencephalopathy-skeletal dysplasia,Early-Onset Epilepsy,Early-onset epilepsy-intellectual disability-brain anomalies syndrome,Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation,Early-Onset epileptic encephalopathy with persistent myelination defect.,Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome,Early-onset generalized limb-onset dystonia,Early-onset Lafora body disease,Early-onset lamellar cataract,Early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria,Early-onset myopathy with fatal cardiomyopathy,Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization,Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome,Early-Onset Neurodegenerative Encephalopathy,Early-onset nuclear cataract,Early-onset parkinsonism-intellectual disability syndrome,Early-onset posterior polar cataract,Early-onset posterior subcapsular cataract,Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome,Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy,Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome,Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome,EARLY-ONSET RECESSIVE OPTIC NEUROPATHY,Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome,Early-Onset Severe Encephalopathy,Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome,Early-onset sutural cataract,EAST syndrome,East Texas bleeding disorder,Ebstein malformation of the tricuspid valve,ECTODERMAL DYSPLASIA 1 HYPOHIDROTIC X-LINKED,ECTODERMAL DYSPLASIA 10A HYPOHIDROTIC/HAIR/NAIL TYPE AUTOSOMAL DOMINANT,Ectodermal dysplasia 10B hypohidrotic/hair/tooth type autosomal recessive,ECTODERMAL DYSPLASIA 11A HYPOHIDROTIC/HAIR/TOOTH TYPE AUTOSOMAL DOMINANT,Ectodermal dysplasia 11b hypohidrotic/hair/tooth type autosomal recessive,ECTODERMAL DYSPLASIA 12 HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE,ECTODERMAL DYSPLASIA 13 HAIR/TOOTH TYPE,ECTODERMAL DYSPLASIA 14 HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS,ECTODERMAL DYSPLASIA 15 HYPOHIDROTIC/HAIR TYPE,Ectodermal dysplasia 4 hair/nail type,Ectodermal dysplasia 7 hair/nail type,ECTODERMAL DYSPLASIA 9 HAIR/NAIL TYPE,ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 1,ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2,Ectodermal dysplasia anhidrotic with immunodeficiency X-linked,ECTODERMAL DYSPLASIA ECTRODACTYLY AND MACULAR DYSTROPHY SYNDROME,ectodermal dysplasia type 1,ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL OCULAR AND BRAIN ANOMALIES,Ectodermal dysplasia-syndactyly syndrome,ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1,Ectodermal dysplasia/short stature syndrome,ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME,ECTOPIA LENTIS 1 ISOLATED AUTOSOMAL DOMINANT,ECTOPIA LENTIS 2 ISOLATED AUTOSOMAL RECESSIVE,ECTOPIA LENTIS ET PUPILLAE,ECTRODACTYLY ECTODERMAL DYSPLASIA AND CLEFT LIP/PALATE SYNDROME 3,ECULIZUMAB POOR RESPONSE TO,EDICT syndrome,EEC syndrome,EEF2-related developmental disorder monoallelic,EEM syndrome,EFAVIRENZ POOR METABOLISM OF EFAVIRENZ CENTRAL NERVOUS SYSTEM TOXICITY SUSCEPTIBILITY TO INCLUDED,EHLERS-DANLOS SYNDROME ARTHROCHALASIA TYPE 1,EHLERS-DANLOS SYNDROME ARTHROCHALASIA TYPE 2,Ehlers-Danlos syndrome cardiac valvular type,EHLERS-DANLOS SYNDROME CLASSIC TYPE 1,EHLERS-DANLOS SYNDROME CLASSIC TYPE 2,EHLERS-DANLOS SYNDROME CLASSIC-LIKE,EHLERS-DANLOS SYNDROME CLASSIC-LIKE 2,Ehlers-Danlos syndrome dermatosparaxis type,Ehlers-Danlos Syndrome Kyphoscoliotic Form,EHLERS-DANLOS SYNDROME KYPHOSCOLIOTIC TYPE 1,EHLERS-DANLOS SYNDROME KYPHOSCOLIOTIC TYPE 2,EHLERS-DANLOS SYNDROME MUSCULOCONTRACTURAL TYPE,EHLERS-DANLOS SYNDROME MUSCULOCONTRACTURAL TYPE 1,EHLERS-DANLOS SYNDROME MUSCULOCONTRACTURAL TYPE 2,EHLERS-DANLOS SYNDROME PERIODONTAL TYPE 1,EHLERS-DANLOS SYNDROME PERIODONTAL TYPE 2,EHLERS-DANLOS SYNDROME PROGEROID TYPE,EHLERS-DANLOS SYNDROME SPONDYLODYSPLASTIC TYPE 1,EHLERS-DANLOS SYNDROME SPONDYLODYSPLASTIC TYPE 2,EHLERS-DANLOS SYNDROME SPONDYLODYSPLASTIC TYPE 3,Ehlers-Danlos syndrome vascular type,Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis Myopathy and Hearing Loss,EHLERS-DANLOS SYNDROME-LIKE SPONDYLOCHEIRODYSPLASIA,Ehlers-Danlos/osteogenesis imperfecta syndrome,EHMT1-LIKE INTELLECTUAL DISABILITY,EHMT1-like SYNDROME,EIF2AK1-associated Neurodevelopmental Syndrome,EIF2AK2-associated Developmental Delay Leukoencephalopathy and Neurologic Decompensation,EIF2B4-RELATED LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER,EIF2B5-RELATED LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER,EIF3F related developmental disorder,EIF5A-related craniofacial-neurodevelopmental disorder,EIKEN SYNDROME,ELLIPTOCYTOSIS 1,ELLIPTOCYTOSIS 2,ELLIPTOCYTOSIS 3,Ellis Van Creveld syndrome,ELLIS-VAN CREVELD SYNDROME,ELN-Related Cutis Laxa,ELSAHY-WATERS SYNDROME,Emberger syndrome,embryonal rhabdomyosarcoma,EMC10-related neurodevelopmental disorder,EMERY-DREIFUSS MUSCULAR DYSTROPHY 1 X-LINKED,EMERY-DREIFUSS MUSCULAR DYSTROPHY 2 AUTOSOMAL DOMINANT,EMERY-DREIFUSS MUSCULAR DYSTROPHY 3 AUTOSOMAL RECESSIVE,Emery-Dreifuss muscular dystrophy 4 autosomal dominant,Emery-dreifuss muscular dystrophy 5 autosomal dominant,Emery-Dreifuss muscular dystrophy 6 X-linked,EMERY-DREIFUSS MUSCULAR DYSTROPHY 7 AUTOSOMAL DOMINANT,Emery-Dreifuss muscular dystrophy type 2,EMILIN-1-related connective tissue disease,Enamel-renal syndrome,ENCEPHALITIS/ENCEPHALOPATHY MILD WITH REVERSIBLE MYELIN VACUOLIZATION,Encephalocraniocutaneous lipomatosis,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 1,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 2,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 5,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 6,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 7,ENCEPHALOPATHY ACUTE INFECTION-INDUCED HERPES-SPECIFIC SUSCEPTIBILITY TO 8,ENCEPHALOPATHY ACUTE INFECTION-INDUCED SUSCEPTIBILITY TO 3,ENCEPHALOPATHY ACUTE INFECTION-INDUCED SUSCEPTIBILITY TO 4,ENCEPHALOPATHY ACUTE INFECTION-INDUCED SUSCEPTIBILITY TO 9,Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2,Encephalopathy due to prosaposin deficiency,ENCEPHALOPATHY ETHYLMALONIC,ENCEPHALOPATHY FAMILIAL WITH NEUROSERPIN INCLUSION BODIES,ENCEPHALOPATHY NEONATAL SEVERE DUE TO MECP2 MUTATIONS,ENCEPHALOPATHY NEONATAL SEVERE WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES,ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH BRAIN ATROPHY AND SPASTICITY,ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM,ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY 1,ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY 2,ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH EPISODIC RHABDOMYOLYSIS,ENCEPHALOPATHY PROGRESSIVE WITH AMYOTROPHY AND OPTIC ATROPHY,Encephalopathy progressive with or without lipodystrophy,Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome,Endocrine-cerebro-osteodysplasia syndrome,ENDOCRINE-CEREBROOSTEODYSPLASIA,Endometrial Cancer,Endometrial stromal sarcoma,Endosteal Hyperostosis and Oligodontia,ENDOSTEAL HYPEROSTOSIS AUTOSOMAL DOMINANT,ENDOSTEAL HYPEROSTOSIS WORTH TYPE,Endosteal sclerosis-cerebellar hypoplasia syndrome,ENDOVE SYNDROME LIMB-BRAIN TYPE,Enhanced Growth and Connective Tissue Abnormalities,ENHANCED S-CONE SYNDROME,Enlarged parietal foramina,Enlarged Parietal Foramina/Cranium Bifidum,ENOLASE SPERM SPECIFIC,Enteric anendocrinosis,ENTEROKINASE DEFICIENCY,Enzalutamide toxicity,EOSINOPHIL PEROXIDASE DEFICIENCY,Ependymoma,EPIDERMODYSPLASIA VERRUCIFORMIS,EPIDERMODYSPLASIA VERRUCIFORMIS SUSCEPTIBILITY TO 1,EPIDERMODYSPLASIA VERRUCIFORMIS SUSCEPTIBILITY TO 2,EPIDERMODYSPLASIA VERRUCIFORMIS SUSCEPTIBILITY TO 3,EPIDERMODYSPLASIA VERRUCIFORMIS SUSCEPTIBILITY TO 4,EPIDERMODYSPLASIA VERRUCIFORMIS SUSCEPTIBILITY TO 5,EPIDERMOLYSIS BULLOSA DYSTROPHICA AUTOSOMAL DOMINANT,EPIDERMOLYSIS BULLOSA DYSTROPHICA AUTOSOMAL RECESSIVE,EPIDERMOLYSIS BULLOSA DYSTROPHICA PRETIBIAL,EPIDERMOLYSIS BULLOSA JUNCTIONAL HERLITZ TYPE,EPIDERMOLYSIS BULLOSA JUNCTIONAL NON-HERLITZ TYPE,EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA,EPIDERMOLYSIS BULLOSA LETHAL ACANTHOLYTIC,EPIDERMOLYSIS BULLOSA NONSPECIFIC AUTOSOMAL RECESSIVE,EPIDERMOLYSIS BULLOSA PRURIGINOSA,EPIDERMOLYSIS BULLOSA SIMPLEX AUTOSOMAL RECESSIVE 1,Epidermolysis bullosa simplex autosomal recessive 2,EPIDERMOLYSIS BULLOSA SIMPLEX DOWLING-MEARA TYPE,Epidermolysis bullosa simplex due to BP230 deficiency,Epidermolysis bullosa simplex due to exophilin 5 deficiency,EPIDERMOLYSIS BULLOSA SIMPLEX GENERALIZED,Epidermolysis bullosa simplex generalized with scarring and hair loss,EPIDERMOLYSIS BULLOSA SIMPLEX LOCALIZED,EPIDERMOLYSIS BULLOSA SIMPLEX OGNA TYPE,Epidermolysis bullosa simplex with circinate migratory erythema,EPIDERMOLYSIS BULLOSA SIMPLEX WITH MIGRATORY CIRCINATE ERYTHEMA,EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION,EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY,Epidermolysis bullosa simplex with nail dystrophy,EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA,EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS,Epidermolysis Bullosa with Pyloric Atresia,EPIDERMOLYTIC HYPERKERATOSIS,Epidermolytic palmoplantar keratoderma,Epilepsy and intellectual disability,EPILEPSY CHILDHOOD ABSENCE SUSCEPTIBILITY TO 5,EPILEPSY CHILDHOOD ABSENCE SUSCEPTIBILITY TO 6,EPILEPSY EARLY-ONSET VITAMIN B6-DEPENDENT,EPILEPSY EARLY-ONSET WITH OR WITHOUT DEVELOPMENTAL DELAY,EPILEPSY FAMILIAL ADULT MYOCLONIC 1,EPILEPSY FAMILIAL ADULT MYOCLONIC 2,EPILEPSY FAMILIAL ADULT MYOCLONIC 3,EPILEPSY FAMILIAL ADULT MYOCLONIC 4,Epilepsy familial adult myoclonic 5,EPILEPSY FAMILIAL ADULT MYOCLONIC 6,EPILEPSY FAMILIAL ADULT MYOCLONIC 7,EPILEPSY FAMILIAL FOCAL WITH VARIABLE FOCI 1,EPILEPSY FAMILIAL FOCAL WITH VARIABLE FOCI 2,EPILEPSY FAMILIAL FOCAL WITH VARIABLE FOCI 3,EPILEPSY FAMILIAL FOCAL WITH VARIABLE FOCI 4,EPILEPSY FAMILIAL TEMPORAL LOBE 1,EPILEPSY FAMILIAL TEMPORAL LOBE 5,EPILEPSY FAMILIAL TEMPORAL LOBE 7,EPILEPSY FAMILIAL TEMPORAL LOBE 8,Epilepsy focal with speech disorder and with or without mental retardation,Epilepsy generalized with febrile seizures plus type 3,EPILEPSY HEARING LOSS AND MENTAL RETARDATION SYNDROME,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 10,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 11,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 12,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 13,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 14,Epilepsy idiopathic generalized susceptibility to 15,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 16,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 8,EPILEPSY IDIOPATHIC GENERALIZED SUSCEPTIBILITY TO 9,EPILEPSY JUVENILE ABSENCE SUSCEPTIBILITY TO 1,EPILEPSY JUVENILE MYOCLONIC SUSCEPTIBILITY TO 10,EPILEPSY NOCTURNAL FRONTAL LOBE 1,EPILEPSY NOCTURNAL FRONTAL LOBE 3,EPILEPSY NOCTURNAL FRONTAL LOBE 4,EPILEPSY NOCTURNAL FRONTAL LOBE 5,Epilepsy progressive myoclonic 10,EPILEPSY PROGRESSIVE MYOCLONIC 11,EPILEPSY PROGRESSIVE MYOCLONIC 12,EPILEPSY PROGRESSIVE MYOCLONIC 1B,EPILEPSY PROGRESSIVE MYOCLONIC 3 WITH OR WITHOUT INTRACELLULAR INCLUSIONS,Epilepsy progressive myoclonic 4 with or without renal failure,EPILEPSY PROGRESSIVE MYOCLONIC 6,Epilepsy progressive myoclonic 7,EPILEPSY PROGRESSIVE MYOCLONIC 8,Epilepsy progressive myoclonic 9,EPILEPSY PYRIDOXINE-DEPENDENT,Epilepsy rolandic with paroxysmal exercise-induced dystonia and writers cramp,Epilepsy with myoclonic-Atonic seizures,EPILEPSY X-LINKED WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR DISORDERS,Epileptic encephalopathy,Epileptic encephalopathy childhood-onset,Epileptic Encephalopathy due to congenital disorder of glycosylation,Epileptic encephalopathy early infantile,Epileptic Encephalopathy Early Infantile 12,Epileptic encephalopathy early infantile 13,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE 23,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE 24,Epileptic encephalopathy early infantile 26,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE 28,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE 3,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 2,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 4,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 5,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 7,EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 9,EPILEPTIC ENCEPHALOPATHY Gain-of-function,EPILEPTIC ENCEPHALOPATHY INFANTILE OR EARLY CHILDHOOD 3,Epileptic encephalopathy Lennox-Gastaut type,EPILEPTIC ENCEPHALOPATHY Loss-of-function,Epileptic encephalopathy with complex movement disorder and regression,Epileptic encephalopathy with continuous spike-and-wave during sleep,Epileptic Encephalopathy with Contractures Macrocephaly and Dyskinesia,Epileptic encephalopathy with global cerebral demyelination,Epileptic Encephalopathy with Optic Atrophy,Epileptic Encephalopathy with Seizure Onset in the First Days of Life,Epimerase-deficiency galactosemia,Epiphyseal chondrodysplasia miura type,EPIPHYSEAL DYSPLASIA MULTIPLE 1,EPIPHYSEAL DYSPLASIA MULTIPLE 2,EPIPHYSEAL DYSPLASIA MULTIPLE 3,EPIPHYSEAL DYSPLASIA MULTIPLE 4,EPIPHYSEAL DYSPLASIA MULTIPLE 5,EPIPHYSEAL DYSPLASIA MULTIPLE 6,EPIPHYSEAL DYSPLASIA MULTIPLE 7,EPIPHYSEAL DYSPLASIA MULTIPLE WITH EARLY-ONSET DIABETES MELLITUS,Epiphyseal dysplasia multiple with myopia and conductive deafness,Episodes of Liver Failure Peripheral Neuropathy Cerebellar Atrophy and Ataxia,Episodic ataxia type 1,EPISODIC ATAXIA TYPE 2,Episodic ataxia type 5,Episodic ataxia type 6,EPISODIC ATAXIA TYPE 9,EPISODIC KINESIGENIC DYSKINESIA 1,EPISODIC PAIN SYNDROME FAMILIAL,EPISODIC PAIN SYNDROME FAMILIAL 1,EPISODIC PAIN SYNDROME FAMILIAL 2,Episodic pain syndrome familial 3,Epithelial basement membrane dystrophy,Epithelial recurrent erosion dystrophy,Epithelioid hemangioendothelioma,EPT1-related complex progressive hereditary spastic paraplegia,ERYTHERMALGIA PRIMARY,ERYTHROCYTE AMP DEAMINASE DEFICIENCY,Erythrocyte galactose epimerase deficiency,ERYTHROCYTE LACTATE TRANSPORTER DEFECT,ERYTHROCYTOSIS FAMILIAL 1,ERYTHROCYTOSIS FAMILIAL 2,ERYTHROCYTOSIS FAMILIAL 3,ERYTHROCYTOSIS FAMILIAL 4,ERYTHROCYTOSIS FAMILIAL 5,ERYTHROCYTOSIS FAMILIAL 6,ERYTHROCYTOSIS FAMILIAL 7,ERYTHROCYTOSIS FAMILIAL 8,Erythroderma congenital with palmoplantar keratoderma hypotrichosis and hyper-ige,ERYTHRODERMA ICHTHYOSIFORM CONGENITAL RETICULAR,Erythrokeratodermia variabilis,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 7,Erythrokeratodermia-cardiomyopathy syndrome,ERYTHROLEUKEMIA FAMILIAL SUSCEPTIBILITY TO,ESOPHAGEAL CANCER ESOPHAGEAL SQUAMOUS CELL CARCINOMA SUSCEPTIBILITY TO INCLUDED,Essential fructosuria,Essential thrombocythemia,ESTROGEN RESISTANCE,Estrogen resistance syndrome,Ethylmalonic encephalopathy,EVEN-PLUS SYNDROME,Ewing sarcoma,EXERCISE INTOLERANCE RIBOFLAVIN-RESPONSIVE,Exercise-induced hyperinsulinism,Exercise-induced malignant hyperthermia,Exfoliation syndrome,Exfoliative ichthyosis,Exfoliative ichthyosis autosomal recessive ichthyosis bullosa of Siemens-like,EXOCRINE PANCREATIC INSUFFICIENCY DYSERYTHROPOIETIC ANEMIA AND CALVARIAL HYPEROSTOSIS,Exostoses multiple type 2,EXOSTOSES MULTIPLE TYPE I,EXOSTOSES MULTIPLE TYPE II,External auditory canal aplasia/hypoplasia,External Ophthalmoplegia Rib and Vertebral Anomalies,EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY,Extraskeletal Ewing sarcoma,Extraskeletal myxoid chondrosarcoma,EXTREME MYOPIA;MYOPIA 23 AUTOSOMAL RECESSIVE,EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE,EXUDATIVE VITREORETINOPATHY 1,EXUDATIVE VITREORETINOPATHY 2 X-LINKED,Exudative vitreoretinopathy 4,EXUDATIVE VITREORETINOPATHY 5,Exudative vitreoretinopathy 6,EXUDATIVE VITREORETINOPATHY 7,F12-related hereditary angioedema with normal C1Inh,FABRY DISEASE,FACIAL CLEFTING OBLIQUE 1,Facial dysmorphism hypertrichosis epilepsy intellectual disability/developmental delay and gingival overgrowth,FACIAL DYSMORPHISM HYPERTRICHOSIS EPILEPSY INTELLECTUAL/DEVELOPMENTAL DELAY AND GINGIVAL OVERGROWTH SYNDROME,FACIAL DYSMORPHISM IMMUNODEFICIENCY LIVEDO AND SHORT STATURE,FACIAL DYSMORPHISM LENS DISLOCATION ANTERIOR SEGMENT ABNORMALITIES AND SPONTANEOUS FILTERING BLEBS,Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion,Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation,Facial dysmorphism-immunodeficiency-livedo-short stature syndrome,Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome,FACIAL PALSY CONGENITAL WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION,FACIAL PARESIS HEREDITARY CONGENITAL 3,Facioscapulohumeral dystrophy,FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1,FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2,FACTOR V AND FACTOR VIII COMBINED DEFICIENCY OF 1,FACTOR V AND FACTOR VIII COMBINED DEFICIENCY OF 2,FACTOR V DEFICIENCY,FACTOR VII DEFICIENCY,FACTOR X DEFICIENCY,FACTOR XI DEFICIENCY,FACTOR XII DEFICIENCY,FACTOR XIII A SUBUNIT DEFICIENCY OF,FACTOR XIII B SUBUNIT DEFICIENCY OF,FADD-related immunodeficiency,FAILURE OF TOOTH ERUPTION PRIMARY,Familial  hyperprolactinemia,Familial abdominal aortic aneurysm,Familial acute necrotizing encephalopathy,Familial adenomatous polyposis 1,FAMILIAL ADENOMATOUS POLYPOSIS 2,FAMILIAL ADENOMATOUS POLYPOSIS 3,FAMILIAL ADENOMATOUS POLYPOSIS 4,Familial adenomatous polyposis due to 5q22.2 microdeletion,FAMILIAL ADVANCED SLEEP-PHASE SYNDROME,Familial afibrinogenemia,Familial Alzheimer-like prion disease,Familial aortic dissection,Familial apolipoprotein A5 deficiency,Familial apolipoprotein C-II deficiency,Familial atrial fibrillation,Familial atrial myxoma,Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease,Familial atypical multiple mole melanoma syndrome,Familial avascular necrosis of femoral head,Familial benign chronic pemphigus,Familial benign flecked retina,Familial bicuspid aortic valve,Familial calcium pyrophosphate deposition,Familial cavitary optic disc anomaly,Familial cerebral cavernous malformation,Familial cerebral saccular aneurysm,Familial Chilblain lupus,Familial clubfoot due to 17q23.1q23.2 microduplication,Familial clubfoot due to 5q31 microdeletion,Familial clubfoot due to PITX1 point mutation,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3,Familial cold autoinflammatory syndrome 4,Familial cold urticaria,Familial colorectal cancer Type X,Familial congenital mirror movements,Familial congenital nasolacrimal duct obstruction,Familial cortical myoclonus,Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome,Familial cylindromatosis,Familial Diarrhea DIARRHEA 6,Familial digital arthropathy-brachydactyly,Familial dilated cardiomyopathy with conduction defect due to LMNA mutation,Familial drusen,Familial dysautonomia,Familial dysfibrinogenemia,Familial dyskinesia and facial myokymia,Familial encephalopathy with neuroserpin inclusion bodies,Familial episodic pain syndrome with predominantly lower limb involvement,Familial episodic pain syndrome with predominantly upper body involvement,FAMILIAL EXPANSILE OSTEOLYSIS,Familial exudative vitreoretinopathy,FAMILIAL FOCAL EPILEPSY WITH VARIABLE FOCI,Familial gastric type 1 neuroendocrine tumor,Familial generalized lentiginosis,Familial gestational hyperthyroidism,Familial glucocorticoid deficiency,Familial GPIHBP1 deficiency,Familial hemophagocytic lymphohistiocytosis,Familial Horizontal Gaze Palsy with Progressive Scoliosis,Familial hyperaldosteronism type I,Familial hyperaldosteronism type III,Familial hypercholanemia,familial hyperinsulinism,Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome,Familial hyperthyroidism due to mutations in TSH receptor,Familial hypoaldosteronism,Familial hypocalciuric hypercalcemia type 1,Familial hypocalciuric hypercalcemia type 2,Familial hypocalciuric hypercalcemia type 3,Familial hypodysfibrinogenemia,Familial hypofibrinogenemia,Familial infantile bilateral striatal necrosis,Familial infantile myoclonic epilepsy,Familial Infantile Myofibromatosis,Familial isolated arrhythmogenic ventricular dysplasia biventricular form,Familial isolated arrhythmogenic ventricular dysplasia left dominant form,Familial isolated arrhythmogenic ventricular dysplasia right dominant form,Familial isolated congenital asplenia,Familial isolated dilated cardiomyopathy,Familial isolated hyperparathyroidism,Familial Isolated Hypoparathyroidism,Familial isolated hypoparathyroidism due to agenesis of parathyroid gland,Familial isolated hypoparathyroidism due to impaired PTH secretion,Familial isolated pituitary adenoma,Familial isolated restrictive cardiomyopathy,Familial isolated trichomegaly,Familial lambdoid synostosis,Familial LCAT deficiency,Familial lipase maturation factor 1 deficiency,Familial lipoprotein lipase deficiency,Familial male-limited precocious puberty,FAMILIAL MEDITERRANEAN FEVER,FAMILIAL MEDITERRANEAN FEVER AUTOSOMAL DOMINANT,Familial medullary thyroid carcinoma,Familial melanoma,Familial mesial temporal lobe epilepsy with febrile seizures,Familial mitral valve prolapse,Familial multinodular goiter,Familial multiple meningioma,Familial multiple nevi flammei,Familial multiple trichoepithelioma,Familial normophosphatemic tumoral calcinosis,Familial or sporadic hemiplegic migraine,Familial osteochondritis dissecans,Familial pancreatic carcinoma,Familial papillary or follicular thyroid carcinoma,Familial paroxysmal ataxia,Familial partial lipodystrophy Dunnigan type,Familial partial lipodystrophy Kobberling type,FAMILIAL PARTIAL LIPODYSTROPHY TYPE 2,Familial patent arterial duct,Familial platelet disorder with associated myeloid malignancy,Familial porencephaly,Familial porphyria cutanea tarda,Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement,Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement,Familial primary hypomagnesemia with normocalciuria and normocalcemia,Familial primary localized cutaneous amyloidosis,Familial progressive cardiac conduction defect,Familial progressive hyper- and hypopigmentation,Familial progressive hyperpigmentation,Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome,Familial prostate cancer,Familial pseudohyperkalemia,Familial renal glucosuria,Familial retinal arterial macroaneurysm,Familial rhabdoid tumor,Familial scaphocephaly syndrome McGillivray type,Familial schizencephaly,FAMILIAL SCHIZENCEPHALY EMX2-RELATED,Familial short QT syndrome,Familial sick sinus syndrome,Familial spontaneous pneumothorax,Familial steroid-resistant nephrotic syndrome with adrenal insufficiency,Familial steroid-resistant nephrotic syndrome with sensorineural deafness,Familial thoracic aortic aneurysm and aortic dissection,Familial thrombocytosis,Familial thyroid dyshormonogenesis,Familial vesicoureteral reflux,Familial visceral myopathy,FANCB-Related Fanconi Anemia,FANCM-Related Fanconi Anemia,Fanconi anemia,Fanconi anemia complementation group 0,FANCONI ANEMIA COMPLEMENTATION GROUP A,FANCONI ANEMIA COMPLEMENTATION GROUP B,Fanconi anemia complementation group C,FANCONI ANEMIA COMPLEMENTATION GROUP D TYPE 1,FANCONI ANEMIA COMPLEMENTATION GROUP D1,FANCONI ANEMIA COMPLEMENTATION GROUP D2,FANCONI ANEMIA COMPLEMENTATION GROUP E,FANCONI ANEMIA COMPLEMENTATION GROUP F,FANCONI ANEMIA COMPLEMENTATION GROUP G,Fanconi anemia complementation group I,FANCONI ANEMIA COMPLEMENTATION GROUP J,FANCONI ANEMIA COMPLEMENTATION GROUP L,FANCONI ANEMIA COMPLEMENTATION GROUP N,Fanconi anemia complementation group O,FANCONI ANEMIA COMPLEMENTATION GROUP P,Fanconi anemia complementation group Q,FANCONI ANEMIA COMPLEMENTATION GROUP R,FANCONI ANEMIA COMPLEMENTATION GROUP S,Fanconi anemia complementation group t,Fanconi anemia complementation group U,FANCONI ANEMIA COMPLEMENTATION GROUP V,FANCONI ANEMIA COMPLEMENTATION GROUP W,Fanconi renotubular syndrome 1,FANCONI RENOTUBULAR SYNDROME 2,FANCONI RENOTUBULAR SYNDROME 3,Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young,FANCONI RENOTUBULAR SYNDROME 5,FANCONI-BICKEL SYNDROME,Farber disease,Farber lipogranulomatosis,FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5,FASTKD2-related infantile mitochondrial encephalomyopathy,Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease,Fatal encephalopathy lactic acidosis and severe mtDNA depletion in muscle,FATAL FAMILIAL INSOMNIA,Fatal Infantile Cardioencephalomyopathy due to Cytochrome c Oxidase Deficiency,Fatal infantile cytochrome C oxidase deficiency,Fatal infantile hypertonic myofibrillar myopathy,Fatal Infantile Lactic Acidosis,Fatal infantile lactic acidosis with methylmalonic aciduria,Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3,Fatal post-viral neurodegenerative disorder,Fatty acid hydroxylase-associated neurodegeneration,Fatty acyl-CoA reductase 1 deficiency,FAZIO-LONDE DISEASE,FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome,FBX028-related developmental and epileptic encephalopathy with profound intellectual disability,FBXW7-related developmental disorder monoallelic,FEBRILE SEIZURES FAMILIAL 11,FEBRILE SEIZURES FAMILIAL 4,FEBRILE SEIZURES FAMILIAL 8,FEINGOLD SYNDROME,FEINGOLD SYNDROME 1,Feingold syndrome type 1,Female infertility due to oocyte meiotic arrest,Female infertility due to zona pellucida defect,Female restricted epilepsy with intellectual disability,Ferro-cerebro-cutaneous syndrome,FETAL AKINESIA DEFORMATION SEQUENCE,FETAL AKINESIA DEFORMATION SEQUENCE 1,FETAL AKINESIA DEFORMATION SEQUENCE 2,FETAL AKINESIA DEFORMATION SEQUENCE 3,FETAL AKINESIA DEFORMATION SEQUENCE 4,Fetal akinesia-cerebral and retinal hemorrhage syndrome,Fetal and neonatal alloimmune thrombocytopenia,Fetal encasement syndrome,Fetal Gaucher disease,FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1,FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6,Fever-associated acute infantile liver failure syndrome,FG SYNDROME 2,FG SYNDROME 4,FG syndrome type 1,FG SYNDROME TYPE 4,FGF13-related neurodevelopmental disorder hemizygous,FGF13-related neurodevelopmental disorder X-linked dominant,FGF14-related episodic ataxia,FGFR2-related bent bone dysplasia,FHEIG (facial dysmorphism hypertrichosis epilepsy intellectual disability/developmental delay and gingival overgrowth),Fibrillary astrocytoma,Fibrochondrogenesis,FIBROCHONDROGENESIS 1,FIBROCHONDROGENESIS 2,FIBRODYSPLASIA OSSIFICANS PROGRESSIVA,Fibrolamellar hepatocellular carcinoma,FIBROMATOSIS GINGIVAL 1,FIBROMATOSIS GINGIVAL 5,Fibronectin glomerulopathy,Fibrosarcoma,FIBROSIS NEURODEGENERATION AND CEREBRAL ANGIOMATOSIS,FIBROSIS OF EXTRAOCULAR MUSCLES CONGENITAL 1,FIBROSIS OF EXTRAOCULAR MUSCLES CONGENITAL 2,Fibrosis of extraocular muscles congenital 3a with or without extraocular involvement,Fibrosis of extraocular muscles congenital 5,FIBULAR APLASIA OR HYPOPLASIA FEMORAL BOWING AND POLY- SYN- AND OLIGODACTYLY,Fibular aplasia-complex brachydactyly syndrome,FICOLIN 3 DEFICIENCY,Filippi syndrome,Filippi syndrome. syndactyly type i with microcephaly and mental retardation,FISH-EYE DISEASE,FKRP-related  limb-girdle muscular dystrophy R9,FLECK CORNEAL DYSTROPHY,FLECK RETINA FAMILIAL BENIGN,FLNA-related X-linked myxomatous valvular dysplasia,FLOATING-HARBOR SYNDROME,FOCAL CORTICAL DYSPLASIA TYPE II,FOCAL DERMAL HYPOPLASIA,Focal epilepsy,Focal epilepsy - intellectual disability - cerebro-cerebellar malformation,FOCAL FACIAL DERMAL DYSPLASIA 3 SETLEIS TYPE,FOCAL FACIAL DERMAL DYSPLASIA 4,Focal facial dermal dysplasia type III,Focal facial dermal dysplasia type IV,Focal palmoplantar keratoderma with joint keratoses,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1,Focal Segmental Glomerulosclerosis 10,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3 SUSCEPTIBILITY TO,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4 SUSCEPTIBILITY TO,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6,Focal segmental glomerulosclerosis 7,Focal segmental glomerulosclerosis 8,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9,FOLATE MALABSORPTION HEREDITARY,Follicular lymphoma,FONTAINE PROGEROID SYNDROME,Formiminoglutamic aciduria,FOVEAL HYPOPLASIA 1,Foveal hypoplasia 2,Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome,Foveal hypoplasia-presenile cataract syndrome,Fowler vasculopaty,FOXG1 syndrome,FOXG1 syndrome due to 14q12 microdeletion,FOXP4-related Developmental Disorder,Fragile X syndrome,FRAGILE X TREMOR/ATAXIA SYNDROME,Fragile X-associated tremor/ataxia syndrome,FRAGILE X-E MENTAL RETARDATION SYNDROME,FRANK-TER HAAR SYNDROME,FRASER SYNDROME,FRASER SYNDROME 1,FRASER SYNDROME 2,FRASER SYNDROME 3,FRASIER SYNDROME,FRAXE intellectual disability,FRAXF syndrome,Free sialic acid storage disease infantile form,Freeman-Sheldon syndrome,Fried syndrome,FRIEDREICH ATAXIA,FRONTOMETAPHYSEAL DYSPLASIA,FRONTOMETAPHYSEAL DYSPLASIA 1,FRONTOMETAPHYSEAL DYSPLASIA 2,FRONTONASAL DYSPLASIA 1,Frontonasal dysplasia 2,FRONTONASAL DYSPLASIA 3,FRONTONASAL DYSPLASIA TYPE 1,FRONTONASAL DYSPLASIA TYPE 3,Frontonasal dysplasia-alopecia-genital anomalies syndrome,Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome,Frontorhiny,FRONTOTEMPORAL DEMENTIA,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1,Frontotemporal dementia and/or amyotrophic lateral sclerosis 2,Frontotemporal dementia and/or amyotrophic lateral sclerosis 3,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4,Frontotemporal dementia and/or amyotrophic lateral sclerosis 5,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 6,Frontotemporal dementia and/or amyotrophic lateral sclerosis 7,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 8,Frontotemporal dementia with motor neuron disease,FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS GRN-RELATED,FRUCTOSE INTOLERANCE HEREDITARY,FRUCTOSE-16-BISPHOSPHATASE DEFICIENCY,FRUCTOSURIA ESSENTIAL,Fryns syndrome,FTH1-related iron overload,Fuchs endothelial corneal dystrophy,FUCOSIDOSIS,FUCOSYLTRANSFERASE 6 DEFICIENCY,FUHRMANN SYNDROME,Fukutin-related  limb-girdle muscular dystrophy R13,FUMARASE DEFICIENCY,Fumaric aciduria,FUNDUS ALBIPUNCTATUS,FUNDUS ALBIPUNCTATUS RETINITIS PUNCTATA ALBESCENS INCLUDED,GABA-TRANSAMINASE DEFICIENCY,GABRIELE-DE VRIES SYNDROME,GALACTOKINASE DEFICIENCY,Galactose mutarotase deficiency,GALACTOSEMIA,GALACTOSEMIA I,Galactosemia II,GALACTOSEMIA III,GALACTOSEMIA IV,GALACTOSIALIDOSIS,GALLBLADDER DISEASE 1,GALLBLADDER DISEASE 4,GALLOWAY-MOWAT SYNDROME,GALLOWAY-MOWAT SYNDROME 1,GALLOWAY-MOWAT SYNDROME 2,GALLOWAY-MOWAT SYNDROME 2 X-LINKED,GALLOWAY-MOWAT SYNDROME 3,GALLOWAY-MOWAT SYNDROME 4,GALLOWAY-MOWAT SYNDROME 5,GALLOWAY-MOWAT SYNDROME 6,GALLOWAY-MOWAT SYNDROME 7,GALLOWAY-MOWAT SYNDROME 8,Galloway-Mowat syndrome: microcephaly and steroid-Resistant nephrotic syndrome,Gamma-aminobutyric acid transaminase deficiency,Gamma-glutamyl transpeptidase deficiency,GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY HEMOLYTIC ANEMIA DUE TO,Gamma-sarcoglycan-related  limb-girdle muscular dystrophy R5,GAND SYNDROME,GAP JUNCTION PROTEIN BETA-3,GAPO syndrome,GARDNER SYNDROME,Gastric adenocarcinoma and proximal polyposis of the stomach,GASTRIC CANCER HEREDITARY DIFFUSE,GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME,Gastrointestinal stromal tumor,GASTROINTESTINAL ULCERATION RECURRENT WITH DYSFUNCTIONAL PLATELETS,GAUCHER DISEASE ATYPICAL DUE TO SAPOSIN C DEFICIENCY,Gaucher disease perinatal lethal,GAUCHER DISEASE TYPE 1,Gaucher disease type 2,Gaucher disease type 3,GAUCHER DISEASE TYPE I,GAUCHER DISEASE TYPE II,GAUCHER DISEASE TYPE III,GAUCHER DISEASE TYPE IIIC,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,GAZE PALSY FAMILIAL HORIZONTAL WITH PROGRESSIVE SCOLIOSIS 1,GAZE PALSY FAMILIAL HORIZONTAL WITH PROGRESSIVE SCOLIOSIS 2 WITH IMPAIRED INTELLECTUAL DEVELOPMENT,GCGR-related hyperglucagonemia,GDF3 multiple malformations,GDF5-related Symphalangism Spectrum Disorder,GDF6 Oculo-Skeletal Syndrome,GELATINOUS DROP-LIKE CORNEAL DYSTROPHY,Geleophysic dysplasia,GELEOPHYSIC DYSPLASIA 1,GELEOPHYSIC DYSPLASIA 2,GELEOPHYSIC DYSPLASIA 3,Gemistocytic astrocytoma,Generalized arterial calcification of infancy,Generalized Arterial Calcification of Infancy and Hypophosphataemic Rickets,GENERALIZED EPILEPSY AND PAROXYSMAL DYSKINESIA,GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS TYPE 1,GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS TYPE 10,GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS TYPE 2,GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS TYPE 9,Generalized epilepsy with febrile seizures-plus,Generalized epilepsy-paroxysmal dyskinesia syndrome,Generalized galactose epimerase deficiency,Generalized glucocorticoid resistance syndrome,Generalized juvenile polyposis/juvenile polyposis coli,Generalized pseudohypoaldosteronism type 1,Generalized pustular psoriasis,Genetic hyperferritinemia without iron overload,Genetic recurrent myoglobinuria,Genetic steroid-resistant nephrotic syndrome,Genetic transient congenital hypothyroidism,Genitopatellar syndrome,GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME,Germinoma of the central nervous system,Geroderma osteodysplastica,GERODERMA OSTEODYSPLASTICUM,GERSTMANN-STRAUSSLER DISEASE,Gerstmann-Straussler-Scheinker syndrome,GHOSAL HEMATODIAPHYSEAL DYSPLASIA,Ghosal hematodiaphyseal syndrome,Giant axonal neuropathy,Giant axonal neuropathy 1,GIANT AXONAL NEUROPATHY 1 AUTOSOMAL RECESSIVE,GIANT AXONAL NEUROPATHY 2 AUTOSOMAL DOMINANT,Giant cell arteritis,Giant cell glioblastoma,GIGYF1-related developmental disorder monoallelic,GIL BLOOD GROUP,GILBERT SYNDROME,GILLES DE LA TOURETTE SYNDROME,Gillespie Syndrome,Gillespie Syndrome monoallelic,GILLESSEN-KAESBACH-NISHIMURA SYNDROME,Gingival fibromatosis-hypertrichosis syndrome,GIST-PLUS SYNDROME,GITELMAN SYNDROME,GLANZMANN THROMBASTHENIA,GLASS SYNDROME,GLAUCOMA 1 OPEN ANGLE A,GLAUCOMA 1 OPEN ANGLE F,GLAUCOMA 1 OPEN ANGLE G,GLAUCOMA 1 OPEN ANGLE O,GLAUCOMA 3 PRIMARY CONGENITAL A,GLAUCOMA 3 PRIMARY CONGENITAL D,GLAUCOMA 3 PRIMARY CONGENITAL E,GLAUCOMA 3 PRIMARY INFANTILE B,GLAUCOMA NORMAL TENSION SUSCEPTIBILITY TO,GLAUCOMA PRIMARY CLOSED-ANGLE,GLAUCOMA PRIMARY OPEN ANGLE,Glaucoma secondary to spherophakia/ectopia lentis and megalocornea,Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome,GLDC-Related Glycine Encephalopathy,GLI2-Related Holoprosencephaly,GLIOMA SUSCEPTIBILITY 1,GLIOMA SUSCEPTIBILITY 2,GLIOMA SUSCEPTIBILITY 3,GLIOMA SUSCEPTIBILITY 9,Gliosarcoma,Global developmental delay absent or hypoplastic corpus callosum and dysmorphic facies,Global Developmental Delay Hypotonia Scoliosis and Cerebellar Atrophy,Global Developmental Delay Hypotonia Scoliosis and Cerebellar Atrophy Biallelic,GLOBAL DEVELOPMENTAL DELAY LUNG CYSTS OVERGROWTH AND WILMS TUMOR,Global Developmental Delay Multiple Malformations,GLOBAL DEVELOPMENTAL DELAY PROGRESSIVE ATAXIA AND ELEVATED GLUTAMINE,GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT,GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES,Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome,Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome,Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome,Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome,GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2,Glomuvenous malformation,GLOMUVENOUS MALFORMATIONS,GLUCOCORTICOID DEFICIENCY 1,GLUCOCORTICOID DEFICIENCY 2,Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency,GLUCOCORTICOID DEFICIENCY 5,GLUCOCORTICOID RESISTANCE GENERALIZED,GLUCOCORTICOID THERAPY RESPONSE TO,Glucose transporter type 1 deficiency syndrome,Glucose-galactose malabsorption,GLUCOSE/GALACTOSE MALABSORPTION,GLUT1 DEFICIENCY SYNDROME 1,GLUT1 DEFICIENCY SYNDROME 2,GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY,Glutamate-cysteine ligase deficiency,GLUTAMINE DEFICIENCY CONGENITAL,GLUTARIC ACIDEMIA I,Glutaric acidemia type 3,GLUTARIC ACIDURIA III,glutaric aciduria type 2A,glutaric aciduria type 2B,glutaric aciduria type 2C,Glutaricacidemia Type 1,Glutaryl-CoA dehydrogenase deficiency,GLUTATHIONE PEROXIDASE DEFICIENCY,GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES HEMOLYTIC ANEMIA DUE TO,Glutathione synthetase deficiency with 5-oxoprolinuria,Glutathione synthetase deficiency without 5-oxoprolinuria,GLUTATHIONURIA,GLYCEROL KINASE 2,Glycerol Kinase Deficiency,Glycerol kinase deficiency adult form,Glycerol kinase deficiency juvenile form,GLYCEROL QUANTITATIVE TRAIT LOCUS,GLYCINE ENCEPHALOPATHY,Glycine Encephalopathy with Arthrogryposis,GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE,GLYCINE N-METHYLTRANSFERASE DEFICIENCY,GLYCOGEN STORAGE DISEASE 0 LIVER,GLYCOGEN STORAGE DISEASE 0 MUSCLE,Glycogen storage disease due to acid maltase deficiency infantile onset,Glycogen storage disease due to acid maltase deficiency late-onset,Glycogen storage disease due to aldolase A deficiency,Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia,Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib,Glycogen storage disease due to glycogen branching enzyme deficiency adult neuromuscular form,Glycogen storage disease due to glycogen branching enzyme deficiency childhood combined hepatic and myopathic form,Glycogen storage disease due to glycogen branching enzyme deficiency childhood neuromuscular form,Glycogen storage disease due to glycogen branching enzyme deficiency congenital neuromuscular form,Glycogen storage disease due to glycogen branching enzyme deficiency fatal perinatal neuromuscular form,Glycogen storage disease due to glycogen branching enzyme deficiency non progressive hepatic form,Glycogen storage disease due to glycogen branching enzyme deficiency progressive hepatic form,Glycogen storage disease due to glycogen debranching enzyme deficiency,Glycogen storage disease due to hepatic glycogen synthase deficiency,Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency,Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency,Glycogen storage disease due to LAMP-2 deficiency,Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency,Glycogen storage disease due to liver glycogen phosphorylase deficiency,Glycogen storage disease due to liver phosphorylase kinase deficiency,Glycogen storage disease due to muscle and heart glycogen synthase deficiency,Glycogen storage disease due to muscle beta-enolase deficiency,Glycogen storage disease due to muscle glycogen phosphorylase deficiency,Glycogen storage disease due to muscle phosphofructokinase deficiency,Glycogen storage disease due to muscle phosphorylase kinase deficiency,Glycogen storage disease due to phosphoglycerate kinase 1 deficiency,Glycogen storage disease due to phosphoglycerate mutase deficiency,GLYCOGEN STORAGE DISEASE Ia,GLYCOGEN STORAGE DISEASE Ib,GLYCOGEN STORAGE DISEASE Ic,GLYCOGEN STORAGE DISEASE II,GLYCOGEN STORAGE DISEASE III,GLYCOGEN STORAGE DISEASE IV,GLYCOGEN STORAGE DISEASE IXa1,GLYCOGEN STORAGE DISEASE IXb,GLYCOGEN STORAGE DISEASE IXc,GLYCOGEN STORAGE DISEASE OF HEART LETHAL CONGENITAL,GLYCOGEN STORAGE DISEASE TYPE II,Glycogen Storage Disease Type III,GLYCOGEN STORAGE DISEASE TYPE IXd,Glycogen Storage Disease Type VI,GLYCOGEN STORAGE DISEASE V,GLYCOGEN STORAGE DISEASE VI,GLYCOGEN STORAGE DISEASE VII,Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency,GLYCOGEN STORAGE DISEASE X,GLYCOGEN STORAGE DISEASE XI,GLYCOGEN STORAGE DISEASE XII,GLYCOGEN STORAGE DISEASE XIII,GLYCOGEN STORAGE DISEASE XV,Glycosylation Disorder Characterized by Intellectual Disability and Autonomic Dysfunction,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18,GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY,GM1 gangliosidosis type 1,GM1 gangliosidosis type 2,GM1 gangliosidosis type 3,GM1-GANGLIOSIDOSIS TYPE I,GM1-GANGLIOSIDOSIS TYPE II,GM1-GANGLIOSIDOSIS TYPE III,GM2 gangliosidosis AB variant,GM2-GANGLIOSIDOSIS AB VARIANT,GM2-GANGLIOSIDOSIS TYPE 1,GM2-GANGLIOSIDOSIS TYPE 2,GM2-GANGLIOSIDOSIS TYPE AB,GM3 synthase deficiency,GMPPB-related  limb-girdle muscular dystrophy R19,GNAI1 syndrome,GNATHODIAPHYSEAL DYSPLASIA,GNB2-related developmental disorder monoallelic,GNB3 Autosomal-Recessive Congenital Stationary Night Blindness.,GNB5-related intellectual disability-cardiac arrhythmia syndrome,GNE myopathy,Goiter multinodular 1 with or without sertoli-leydig cell tumors,GOLDBERG-SHPRINTZEN MEGACOLON SYNDROME,GOLDBERG-SHPRINTZEN SYNDROME,Goldmann-Favre syndrome,Gollop-Wolfgang complex,Gomez-Lopez-Fernandes syndrome,GONADAL DYSGENESIS DYSMORPHIC FACIES RETINAL DYSTROPHY AND MYOPATHY,GORDON HOLMES SYNDROME,Gordon syndrome,Gorlin syndrome,Gorlin-Chaudhry-Moss syndrome,Gorlin-Chaudhry-Moss syndrome (GCMS);  Syndrome with Hypertrichosis Progeroid Appearance and Mitochondrial Dysfunction,GRACILE BONE DYSPLASIA,GRACILE SYNDROME,GRAFT-VERSUS-HOST DISEASE SUSCEPTIBILITY TO,Graham Little-Piccardi-Lassueur syndrome,GRANGE SYNDROME,Granular corneal dystrophy type I,Granular corneal dystrophy type II,Granulomatosis with polyangiitis,GRANULOMATOUS DISEASE CHRONIC AUTOSOMAL RECESSIVE 1,GRANULOMATOUS DISEASE CHRONIC AUTOSOMAL RECESSIVE 2,GRANULOMATOUS DISEASE CHRONIC AUTOSOMAL RECESSIVE 3,GRANULOMATOUS DISEASE CHRONIC AUTOSOMAL RECESSIVE 4,GRANULOMATOUS DISEASE CHRONIC AUTOSOMAL RECESSIVE 5,GRANULOMATOUS DISEASE CHRONIC X-LINKED,GRAY PLATELET SYNDROME,Greenberg dysplasia,GREIG CEPHALOPOLYSYNDACTYLY SYNDROME,GRIA2-related developmental disorder monoallelic,GRID2-related cerebellar ataxia biallelic,GRID2-related cerebellar ataxia monoallelic,Griscelli syndrome type 1,Griscelli syndrome type 2,Griscelli syndrome type 3,Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome,Growth delay due to insulin-like growth factor I resistance,Growth delay due to insulin-like growth factor type 1 deficiency,Growth delay-intellectual disability-hepatopathy syndrome,GROWTH HORMONE DEFICIENCY ISOLATED PARTIAL,GROWTH HORMONE INSENSITIVITY PARTIAL,GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 1 AUTOSOMAL RECESSIVE,GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 2 AUTOSOMAL DOMINANT,GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY,GROWTH RETARDATION DEVELOPMENTAL DELAY AND FACIAL DYSMORPHISM,GROWTH RETARDATION DEVELOPMENTAL DELAY COARSE FACIES AND EARLY DEATH,GROWTH RETARDATION IMPAIRED INTELLECTUAL DEVELOPMENT HYPOTONIA ANDHEPATOPATHY,Growth Retardation with Prenatal Onset Intellectual Disability Muscular Hypotonia and Infantile Hepatopathy,Growth retardation-mild developmental delay-chronic hepatitis syndrome,GTP CYCLOHYDROLASE 1 DEFICIENCY,GTP cyclohydrolase I deficiency,GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY,GUILLAIN-BARRE SYNDROME FAMILIAL,Guttmacher syndrome,Gynandroblastoma,GYRATE ATROPHY OF CHOROID AND RETINA,H syndrome,HACD1-related congenital myopathy,HACE1 related disorder,Haddad syndrome,Haim-Munk syndrome,HAIR MORPHOLOGY 1,Hairy cell leukemia variant,Hajdu-Cheney syndrome,HALLERMANN-STREIFF SYNDROME,HAMAMY SYNDROME,Hamel cerebro-palato-cardiac syndrome,HANAC syndrome,HAND-FOOT-GENITAL SYNDROME,HAO-FOUNTAIN SYNDROME,Harderoporphyria,HAREL-YOON SYNDROME,HARLEQUIN ICHTHYOSIS,Hartnup disease,HARTNUP DISORDER,HARTSFIELD SYNDROME,HASHIMOTO THYROIDITIS,HAWKINSINURIA,Hb Bart's Hydrops Fetalis,Hearing loss,HEART AND BRAIN MALFORMATION SYNDROME,Heart defect-tongue hamartoma-polysyndactyly syndrome,HEART DEFECTS CONGENITAL AND OTHER CONGENITAL ANOMALIES,HEART-HAND SYNDROME SLOVENIAN TYPE,HEIMLER SYNDROME 1,HEIMLER SYNDROME 2,HEINZ BODY ANEMIAS,HELICOBACTER PYLORI INFECTION SUSCEPTIBILITY TO,Helicoid peripapillary chorioretinal degeneration,HELIX SYNDROME,HELLP syndrome,HELSMOORTEL-VAN DER AA SYNDROME,HEMANGIOMA CAPILLARY INFANTILE,HEMATURIA BENIGN FAMILIAL,HEME OXYGENASE 1 DEFICIENCY,Hemihyperplasia-multiple lipomatosis syndrome,Hemimegalencephaly,Hemimegalencephaly AKT3,Hemimegalencephaly PIK3CA,HEMOCHROMATOSIS TYPE 1,Hemochromatosis type 2,HEMOCHROMATOSIS TYPE 2A,HEMOCHROMATOSIS TYPE 2B,Hemochromatosis type 3,Hemochromatosis type 4,Hemochromatosis type 5,Hemoglobin C disease,Hemoglobin C-beta-thalassemia syndrome,Hemoglobin D disease,Hemoglobin E disease,Hemoglobin E-beta-thalassemia syndrome,HEMOGLOBIN H DISEASE,HEMOGLOBIN HIGH ALTITUDE ADAPTATION,Hemoglobin Lepore-beta-thalassemia syndrome,Hemoglobin M disease,Hemoglobinopathy Toms River,HEMOLYTIC ANEMIA CD59-MEDIATED WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY,HEMOLYTIC ANEMIA CONGENITAL X-LINKED,Hemolytic anemia due to adenylate kinase deficiency,Hemolytic anemia due to diphosphoglycerate mutase deficiency,Hemolytic anemia due to glucophosphate isomerase deficiency,Hemolytic anemia due to glutathione reductase deficiency,Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency,Hemolytic anemia due to red cell pyruvate kinase deficiency,HEMOLYTIC ANEMIA DUE TO UMPH1 DEFICIENCY,HEMOLYTIC ANEMIA NONSPHEROCYTIC DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY,HEMOLYTIC ANEMIA NONSPHEROCYTIC DUE TO HEXOKINASE DEFICIENCY,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 1,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 2,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 3,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 4,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 5,HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 6,Hemolytic uremic syndrome with DGKE deficiency,HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS FAMILIAL 2,HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS FAMILIAL 3,HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS FAMILIAL 4,HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS FAMILIAL 5,HEMOPHILIA A,HEMOPHILIA B,HEMORRHAGE INTRACEREBRAL SUSCEPTIBILITY TO,Hemorrhagic destruction of the brain subependymal calcification and cataracts,Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3,Hennekam syndrome,HEPARIN COFACTOR II DEFICIENCY,HEPATIC ADENOMAS FAMILIAL,HEPATIC LIPASE DEFICIENCY,Hepatic veno-occlusive disease-immunodeficiency syndrome,HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY,HEPATITIS B VIRUS SUSCEPTIBILITY TO,HEPATITIS C VIRUS SUSCEPTIBILITY TO,HEPATITIS FULMINANT VIRAL SUSCEPTIBILITY TO,Hepatocellular Carcinoma,Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1,Hepatoerythropoietic porphyria,Hereditary 125-dihydroxyvitamin D-resistant rickets,Hereditary angioedema type 1,Hereditary angioedema type 2,Hereditary arterial and articular multiple calcification syndrome,Hereditary breast and ovarian cancer syndrome,Hereditary breast cancer,Hereditary central diabetes insipidus,Hereditary chronic pancreatitis,Hereditary clear cell renal cell carcinoma,Hereditary combined deficiency of vitamin K-dependent clotting factors,Hereditary continuous muscle fiber activity,Hereditary coproporphyria,Hereditary cryohydrocytosis with normal stomatin,Hereditary cryohydrocytosis with reduced stomatin,Hereditary diffuse gastric cancer,Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia,Hereditary elliptocytosis,Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome,Hereditary folate malabsorption,Hereditary fructose intolerance,Hereditary gingival fibromatosis,HEREDITARY HEMORRHAGIC TELANGIECTASIA,Hereditary hypercarotenemia and vitamin A deficiency,Hereditary hyperekplexia,HEREDITARY HYPERFERRITINEMIA-CATARACT SYNDROME,Hereditary hypophosphatemic rickets with hypercalciuria,Hereditary hypotrichosis with recurrent skin vesicles,Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome,Hereditary isolated aplastic anemia,Hereditary late-onset Parkinson disease,HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER,Hereditary methemoglobinemia,Hereditary mixed polyposis syndrome,Hereditary motor and sensory neuropathy Okinawa type,Hereditary motor and sensory neuropathy type 5,Hereditary motor and sensory neuropathy type 6,HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE IIC,HEREDITARY MULTIPLE EXOSTOSES TYPE 1,Hereditary Myopathy with Early Respiratory Failure,Hereditary myopathy with lactic acidosis due to ISCU deficiency,Hereditary neuroendocrine tumor of small intestine,Hereditary neuropathy with liability to pressure palsies,Hereditary neutrophilia,Hereditary North American Indian childhood cirrhosis,Hereditary orotic aciduria,Hereditary palmoplantar keratoderma Gamborg-Nielsen type,Hereditary papillary renal cell carcinoma,Hereditary pediatric Behcet-like disease,Hereditary persistence of alpha-fetoprotein,Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome,Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome,Hereditary pheochromocytoma-paraganglioma,Hereditary pulmonary alveolar proteinosis,Hereditary renal hypouricemia,Hereditary retinoblastoma,Hereditary sensorimotor neuropathy with hyperelastic skin,Hereditary sensory and autonomic neuropathy due to TECPR2 mutation,Hereditary sensory and autonomic neuropathy type 1,Hereditary sensory and autonomic neuropathy type 2,Hereditary sensory and autonomic neuropathy type 4,Hereditary sensory and autonomic neuropathy type 5,Hereditary sensory and autonomic neuropathy type 6,Hereditary sensory and autonomic neuropathy type 7,Hereditary sensory and autonomic neuropathy type 8,Hereditary sensory and autonomic neuropathy type VIII,Hereditary sensory neuropathy-deafness-dementia syndrome,Hereditary site-specific ovarian cancer syndrome,Hereditary Spastic Paraparesis,Hereditary Spastic Paraplegia,Hereditary spherocytosis,Hereditary thrombocytopenia with early-onset myelofibrosis,Hereditary thrombophilia due to congenital antithrombin deficiency,Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,Heritable pulmonary arterial hypertension,Hermansky-Pudlak Syndrome,HERMANSKY-PUDLAK SYNDROME 1,Hermansky-Pudlak Syndrome 10,HERMANSKY-PUDLAK SYNDROME 11,HERMANSKY-PUDLAK SYNDROME 2,HERMANSKY-PUDLAK SYNDROME 3,HERMANSKY-PUDLAK SYNDROME 4,Hermansky-Pudlak syndrome 5,HERMANSKY-PUDLAK SYNDROME 6,HERMANSKY-PUDLAK SYNDROME 7,HERMANSKY-PUDLAK SYNDROME 8,Hermansky-Pudlak syndrome 9,Hermansky-Pudlak syndrome type 7,Hermansky-Pudlak syndrome type 8,Hermansky-Pudlak syndrome type 9,Hermansky-Pudlak syndrome with neutropenia,Hermansky-Pudlak syndrome with pulmonary fibrosis,Hermansky-Pudlak syndrome without pulmonary fibrosis,Herpes simplex virus encephalitis,HESX1-Related Combined Pituitary Hormone Deficiency,Heterotaxy Syndrome,HETEROTAXY VISCERAL 1 X-LINKED,HETEROTAXY VISCERAL 2 AUTOSOMAL,HETEROTAXY VISCERAL 4 AUTOSOMAL,HETEROTAXY VISCERAL 5 AUTOSOMAL,HETEROTAXY VISCERAL 6 AUTOSOMAL,HETEROTAXY VISCERAL 7 AUTOSOMAL,HETEROTAXY VISCERAL 8 AUTOSOMAL,HETEROTAXY VISCERAL 9 AUTOSOMAL WITH MALE INFERTILITY,HEYN-SPROUL-JACKSON SYNDROME,HIBCH deficiency,Hidrotic ectodermal dysplasia,High bone mass osteogenesis imperfecta,HIGH BONE MASS TRAIT,HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12,HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6,High grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement,HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY,High myopia-sensorineural deafness syndrome,Hip dysplasia beukes type,HIRA-related neurodevelopmental disorder,Hirschprung disease with intestinal pseudo-obstruction,Hirschsprung disease,HIRSCHSPRUNG DISEASE CARDIAC DEFECTS AND AUTONOMIC DYSFUNCTION,HIRSCHSPRUNG DISEASE SUSCEPTIBILITY TO 1,HIRSCHSPRUNG DISEASE SUSCEPTIBILITY TO 2,HIRSCHSPRUNG DISEASE SUSCEPTIBILITY TO 3,HIRSCHSPRUNG DISEASE SUSCEPTIBILITY TO 4,Hirschsprung disease-ganglioneuroblastoma syndrome,HIST1H2AC-related developmental disorder monoallelic,HIST1H4C,HISTIDINEMIA,Histiocytoid cardiomyopathy,HISTIOCYTOMA ANGIOMATOID FIBROUS,HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME,HIVEP2 associated syndromic developmental delay with intellectual disability,HK1-related developmental disorder monoallelic,HNF1B-related autosomal dominant tubulointerstitial kidney disease,HNF4A-Related Maturity-Onset Diabetes of the Young Type 1,HNRNPD-related developmental disorder monoallelic,HNRNPDL-related  limb-girdle muscular dystrophy D3,HNRNPH1-related neurodevelopmental disorder,HOLOCARBOXYLASE SYNTHETASE DEFICIENCY,Holoprosencephaly,Holoprosencephaly 11,HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS,HOLOPROSENCEPHALY 13 X-LINKED,HOLOPROSENCEPHALY 2,HOLOPROSENCEPHALY 3,HOLOPROSENCEPHALY 4,HOLOPROSENCEPHALY 5,HOLOPROSENCEPHALY 7,HOLOPROSENCEPHALY 9,HOLOPROSENCEPHALY TYPE 3,HOLOPROSENCEPHALY-7,HOLT-ORAM SYNDROME,Homeotic Arm-to-Leg Transformation Associated with Genomic Rearrangements at the PITX1 Locus,HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY,HOMOCYSTINURIA DUE TO DEFICIENCY OF N(510)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY,Homocystinuria due to methylene tetrahydrofolate reductase deficiency,Homocystinuria-megaloblastic anemia cbl E type,HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA cblE COMPLEMENTATION TYPE,HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA cblG COMPLEMENTATION TYPE,Homozygous familial hypercholesterolemia,Horizontal gaze palsy with progressive scoliosis,Hot water reflex epilepsy,HOYERAAL-HREIDARSSON SYNDROME,HPDL Neurodegenerative Disease,HS2ST1-related Developmental Disorder,HSD10 disease atypical type,HSD10 disease infantile type,HSD10 disease neonatal type,HSD10 MITOCHONDRIAL DISEASE,HTRA1-related autosomal dominant cerebral small vessel disease,HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 SUSCEPTIBILITY TO,human piebaldism,HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY,HUNTINGTON DISEASE,HUNTINGTON DISEASE-LIKE 1,HUNTINGTON DISEASE-LIKE 2,Huntington disease-like syndrome due to C9ORF72 expansions,Huriez syndrome,HURLER SYNDROME,HURLER-SCHEIE SYNDROME,HUTCHINSON-GILFORD PROGERIA SYNDROME,Hyaline body myopathy,HYALINE FIBROMATOSIS SYNDROME,Hyaluronidase deficiency,HYDATIDIFORM MOLE RECURRENT 1,HYDATIDIFORM MOLE RECURRENT 2,HYDATIDIFORM MOLE RECURRENT 3,HYDATIDIFORM MOLE RECURRENT 4,Hydranencephaly,HYDROCEPHALUS CONGENITAL 1,HYDROCEPHALUS CONGENITAL 2 WITH OR WITHOUT BRAIN OR EYE ANOMALIES,HYDROCEPHALUS CONGENITAL 3 WITH BRAIN ANOMALIES,HYDROCEPHALUS CONGENITAL COMMUNICATING 1,HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS,HYDROCEPHALUS DUE TO STENOSIS OF THE AQUEDUCT OF SYLVIUS,HYDROCEPHALUS NONSYNDROMIC AUTOSOMAL RECESSIVE,HYDROCEPHALUS NONSYNDROMIC AUTOSOMAL RECESSIVE 2,HYDROCEPHALUS NORMAL-PRESSURE 1,Hydrocephalus with stenosis of the aqueduct of Sylvius,Hydrolethalus,HYDROLETHALUS SYNDROME 1,HYDROLETHALUS SYNDROME 2,HYDROLETHALUS SYNDROME TYPE 1,HYDROPS LACTIC ACIDOSIS AND SIDEROBLASTIC ANEMIA,HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA,Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome,HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY,Hydroxykynureninuria,HYPER-IgD SYNDROME,HYPER-IgE RECURRENT INFECTION SYNDROME 1 AUTOSOMAL DOMINANT,HYPER-IgE RECURRENT INFECTION SYNDROME 2 AUTOSOMAL RECESSIVE,HYPER-IgE RECURRENT INFECTION SYNDROME 3 AUTOSOMAL RECESSIVE,HYPER-IgE RECURRENT INFECTION SYNDROME 4 AUTOSOMAL RECESSIVE,HYPER-IgE RECURRENT INFECTION SYNDROME 5 AUTOSOMAL RECESSIVE,Hyper-IgM syndrome type 2,Hyper-IgM syndrome type 3,Hyper-IgM syndrome type 5,Hyperaldosteronism familial type I,Hyperaldosteronism familial type II,HYPERALDOSTERONISM FAMILIAL TYPE III,HYPERALDOSTERONISM FAMILIAL TYPE IV,HYPERALPHALIPOPROTEINEMIA 1,Hyperammonemia due to carbonic anhydrase VA deficiency,Hyperammonemia due to N-acetylglutamate synthase deficiency,Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency,Hyperandrogenism due to cortisone reductase deficiency,HYPERBILIRUBINEMIA ROTOR TYPE,Hyperbilirubinemia transient familial neonatal,HYPERBILIVERDINEMIA,HYPERCALCEMIA INFANTILE 1,HYPERCALCEMIA INFANTILE 2,HYPERCALCIURIA ABSORPTIVE 2,HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY AUTOSOMAL DOMINANT,Hyperchlorhidrosis isolated,HYPERCHOLANEMIA FAMILIAL,Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency,HYPERCHOLESTEROLEMIA FAMILIAL 1,HYPERCHOLESTEROLEMIA FAMILIAL 2,HYPERCHOLESTEROLEMIA FAMILIAL 3,HYPERCHOLESTEROLEMIA FAMILIAL 4,Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency,Hyperekplexia,HYPEREKPLEXIA 1,HYPEREKPLEXIA 2,HYPEREKPLEXIA 3,HYPEREKPLEXIA 4,Hyperekplexia-epilepsy syndrome,HYPEREOSINOPHILIC SYNDROME IDIOPATHIC,HYPERFERRITINEMIA WITH OR WITHOUT CATARACT,HYPERGLYCINEMIA LACTIC ACIDOSIS AND SEIZURES,HYPERGLYCINURIA,HYPERIMMUNOGLOBULIN E RECURRENT INFECTION SYNDROME AUTOSOMAL RECESSIVE,Hyperimmunoglobulinemia D with periodic fever,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 1,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 2,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 3,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 4,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 5,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 6,HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 7,Hyperinsulinism due to glucokinase deficiency,Hyperinsulinism due to HNF1A deficiency,Hyperinsulinism due to HNF4A deficiency,Hyperinsulinism due to INSR deficiency,Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency,Hyperinsulinism due to UCP2 deficiency,Hyperinsulinism-hyperammonemia syndrome,HYPERKALEMIC PERIODIC PARALYSIS,Hyperkalemic Periodic Paralysis Type 1,Hyperlipidemia due to hepatic triacylglycerol lipase deficiency,HYPERLIPIDEMIA FAMILIAL COMBINED 1,HYPERLIPIDEMIA FAMILIAL COMBINED 3,Hyperlipoproteinemia type I,HYPERLIPOPROTEINEMIA TYPE ID,HYPERLIPOPROTEINEMIA TYPE III,HYPERLIPOPROTEINEMIA TYPE V,HYPERLYSINEMIA,HYPERLYSINEMIA TYPE I,HYPERMANGANESEMIA WITH DYSTONIA 1,HYPERMANGANESEMIA WITH DYSTONIA 2,HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY,Hypermethioninemia due to glycine N-methyltransferase deficiency,Hypermethioninemia encephalopathy due to adenosine kinase deficiency,HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY,Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome,HYPEROSTOSIS CORTICALIS GENERALISATA,HYPEROSTOSIS CRANIALIS INTERNA,Hyperoxaluria Primary Type 1,HYPEROXALURIA PRIMARY TYPE I,HYPEROXALURIA PRIMARY TYPE II,HYPEROXALURIA PRIMARY TYPE III,HYPERPARATHYROIDISM 1,HYPERPARATHYROIDISM 2 WITH JAW TUMORS,HYPERPARATHYROIDISM 4,HYPERPARATHYROIDISM NEONATAL SEVERE,HYPERPARATHYROIDISM TRANSIENT NEONATAL,HYPERPARATHYROIDISM-JAW TUMOR SYNDROME,HYPERPHENYLALANINEMIA BH4-DEFICIENT A,HYPERPHENYLALANINEMIA BH4-DEFICIENT B,HYPERPHENYLALANINEMIA BH4-DEFICIENT C,HYPERPHENYLALANINEMIA BH4-DEFICIENT D,Hyperphenylalaninemia due to DNAJC12 deficiency,Hyperphenylalaninemia Dystonia and Intellectual Disability,HYPERPHENYLALANINEMIA MILD NON-BH4-DEFICIENT,HYPERPHOSPHATASIA WITH MENTAL RETARDATION,HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1,HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2,HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3,Hyperphosphatasia with mental retardation syndrome 4,Hyperphosphatasia with mental retardation syndrome 5,Hyperphosphatasia with mental retardation syndrome 6,Hyperphosphatasia-intellectual disability syndrome,HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION FAMILIAL PROGRESSIVE,Hyperproinsulinemia,HYPERPROLACTINEMIA,Hyperprolinemia type 1,HYPERPROLINEMIA TYPE 2,HYPERPROLINEMIA TYPE I,HYPERPROLINEMIA TYPE II,HYPERTELORISM SEVERE WITH MIDFACE PROMINENCE MYOPIA MENTAL RETARDATION AND BONE FRAGILITY,Hypertelorism Teebi type,HYPERTENSION AND BRACHYDACTYLY SYNDROME,HYPERTENSION DIASTOLIC RESISTANCE TO,HYPERTENSION EARLY-ONSET AUTOSOMAL DOMINANT WITH SEVERE EXACERBATIONIN PREGNANCY,HYPERTENSION ESSENTIAL,HYPERTHYROIDISM FAMILIAL GESTATIONAL,HYPERTHYROIDISM NONAUTOIMMUNE,HYPERTHYROXINEMIA DYSTRANSTHYRETINEMIC,HYPERTHYROXINEMIA FAMILIAL DYSALBUMINEMIC,HYPERTRICHOSIS CONGENITAL GENERALIZED WITH OR WITHOUT GINGIVALHYPERPLASIA,Hypertrichosis-acromegaloid facial appearance syndrome,Hypertrichotic osteochondrodysplasia Cantu type,HYPERTRIGLYCERIDEMIA FAMILIAL,HYPERTRIGLYCERIDEMIA TRANSIENT INFANTILE,Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation,HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS,HYPERTROPHIC OSTEOARTHROPATHY PRIMARY AUTOSOMAL RECESSIVE 1,HYPERTROPHIC OSTEOARTHROPATHY PRIMARY AUTOSOMAL RECESSIVE 2,Hypertryptophanemia,HYPERURICEMIA HPRT-RELATED,HYPERURICEMIA PULMONARY HYPERTENSION RENAL FAILURE AND ALKALOSISSYNDROME,Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome,Hypervalinemia and hyperleucine-isoleucinemia,Hyperzincemia and hypercalprotectinemia,HYPOALPHALIPOPROTEINEMIA PRIMARY 1,HYPOALPHALIPOPROTEINEMIA PRIMARY 2,HYPOBETALIPOPROTEINEMIA FAMILIAL 1,HYPOBETALIPOPROTEINEMIA FAMILIAL 2,HYPOCALCEMIA AUTOSOMAL DOMINANT 1,Hypocalcemia autosomal dominant 2,Hypocalcemic vitamin D dependent rickets,Hypocalcemic vitamin D-resistant rickets,Hypocalcified amelogenesis imperfecta,HYPOCALCIURIC HYPERCALCEMIA FAMILIAL TYPE I,Hypocalciuric hypercalcemia familial type II,HYPOCALCIURIC HYPERCALCEMIA FAMILIAL TYPE III,Hypochondrogenesis,HYPOCHONDROPLASIA,Hypocomplementemic urticarial vasculitis,Hypodontia-dysplasia of nails syndrome,HYPOGLYCEMIA LEUCINE-INDUCED,HYPOGONADOTROPIC HYPOGONADISM,Hypogonadotropic hypogonadism 1 with or without anosmia,Hypogonadotropic hypogonadism 10 with or without anosmia,HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA,Hypogonadotropic hypogonadism 14 with or without anosmia,HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA,Hypogonadotropic hypogonadism 16 with or without anosmia,Hypogonadotropic hypogonadism 17 with or without anosmia,Hypogonadotropic hypogonadism 18 with or without anosmia,Hypogonadotropic hypogonadism 19 with or without anosmia,HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA,Hypogonadotropic hypogonadism 20 with or without anosmia,Hypogonadotropic hypogonadism 21 with or without anosmia,HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA,HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA,Hypogonadotropic hypogonadism 7 with or without anosmia,Hypogonadotropic hypogonadism 8 with or without anosmia,HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA,Hypogonadotropic hypogonadism with or without anosmia,Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome,Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome,Hypohidrotic ectodermal dysplasia with immunodeficiency,Hypoinsulinemic hypoglycemia and body hemihypertrophy,HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY,Hypokalemic periodic paralysis,HYPOKALEMIC PERIODIC PARALYSIS TYPE 1,HYPOKALEMIC PERIODIC PARALYSIS TYPE 2,HYPOMAGNESEMIA 1 INTESTINAL,HYPOMAGNESEMIA 2 RENAL,HYPOMAGNESEMIA 3 RENAL,HYPOMAGNESEMIA 4 RENAL,HYPOMAGNESEMIA 5 RENAL WITH OCULAR INVOLVEMENT,HYPOMAGNESEMIA 5 RENAL WITH OR WITHOUT OCULAR INVOLVEMENT,HYPOMAGNESEMIA 6 RENAL,HYPOMAGNESEMIA SEIZURES AND MENTAL RETARDATION 1,HYPOMAGNESEMIA SEIZURES AND MENTAL RETARDATION 2,Hypomaturation amelogenesis imperfecta,Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism,Hypomyelinating Leukodystrophy,Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome,Hypomyelination neuropathy-arthrogryposis syndrome,Hypomyelination with atrophy of basal ganglia and cerebellum,HYPOMYELINATION WITH ATROPHY OF THE BASAL GANGLIA AND CEREBELLUM,HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY,Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome,Hypomyelination-congenital cataract syndrome,Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome,HYPOPARATHYROIDISM FAMILIAL ISOLATED 1,HYPOPARATHYROIDISM FAMILIAL ISOLATED 2,HYPOPARATHYROIDISM SENSORINEURAL DEAFNESS AND RENAL DISEASE,HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME,Hypoparathyroidism-sensorineural deafness-renal disease syndrome,Hypophosphatasia,HYPOPHOSPHATASIA ADULT,HYPOPHOSPHATASIA CHILDHOOD,HYPOPHOSPHATASIA INFANTILE,Hypophosphatemic rickets AR,HYPOPHOSPHATEMIC RICKETS AUTOSOMAL DOMINANT,HYPOPHOSPHATEMIC RICKETS AUTOSOMAL RECESSIVE 1,HYPOPHOSPHATEMIC RICKETS AUTOSOMAL RECESSIVE 2,HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA HEREDITARY,HYPOPHOSPHATEMIC RICKETS X-LINKED DOMINANT,HYPOPHOSPHATEMIC RICKETS X-LINKED RECESSIVE,HYPOPIGMENTATION ORGANOMEGALY AND DELAYED MYELINATION AND DEVELOPMENT,Hypopigmentation-punctate palmoplantar keratoderma syndrome,Hypoplasminogenemia,Hypoplastic amelogenesis imperfecta,HYPOPLASTIC LEFT HEART SYNDROME,HYPOPLASTIC LEFT HEART SYNDROME 1,HYPOPLASTIC LEFT HEART SYNDROME 2,Hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome,Hypoplastic tibiae-postaxial polydactyly syndrome,Hypoprebetalipoproteinemia acanthocytosis retinitis pigmentosa and pallidal degeneration,Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome,HYPOSPADIAS 1 X-LINKED,HYPOSPADIAS 2 X-LINKED,Hypothryoidism congenital nongoitrous 4,HYPOTHYROIDISM CENTRAL WITH TESTICULAR ENLARGEMENT,HYPOTHYROIDISM CONGENITAL NONGOITROUS 1,HYPOTHYROIDISM CONGENITAL NONGOITROUS 2,HYPOTHYROIDISM CONGENITAL NONGOITROUS 4,HYPOTHYROIDISM CONGENITAL NONGOITROUS 5,HYPOTHYROIDISM CONGENITAL NONGOITROUS 6,HYPOTHYROIDISM CONGENITAL NONGOITROUS 7,HYPOTHYROIDISM CONGENITAL NONGOITROUS 8,HYPOTHYROIDISM CONGENITAL NONGOITROUS 9,Hypothyroidism due to deficient transcription factors involved in pituitary development or function,Hypothyroidism due to TSH receptor mutations,HYPOTHYROIDISM THYROIDAL OR ATHYROIDAL WITH SPIKY HAIR AND CLEFTPALATE,HYPOTONIA ATAXIA AND DELAYED DEVELOPMENT SYNDROME,HYPOTONIA ATAXIA DEVELOPMENTAL DELAY AND TOOTH ENAMEL DEFECT SYNDROME,HYPOTONIA HYPOVENTILATION IMPAIRED INTELLECTUAL DEVELOPMENT DYSAUTONOMIA EPILEPSY AND EYE ABNORMALITIES,HYPOTONIA INFANTILE WITH PSYCHOMOTOR RETARDATION,HYPOTONIA INFANTILE WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES,Hypotonia infantile with psychomotor retardation and characteristic facies 1,HYPOTONIA INFANTILE WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2,Hypotonia infantile with psychomotor retardation and characteristic facies 3,Hypotonia with lactic acidemia and hyperammonemia,HYPOTONIA-CYSTINURIA SYNDROME,Hypotonia-speech impairment-severe cognitive delay syndrome,HYPOTRICHOSIS 1,HYPOTRICHOSIS 11,Hypotrichosis 12,Hypotrichosis 13,HYPOTRICHOSIS 14,HYPOTRICHOSIS 2,HYPOTRICHOSIS 3,HYPOTRICHOSIS 4,HYPOTRICHOSIS 5,HYPOTRICHOSIS 6,HYPOTRICHOSIS 7,HYPOTRICHOSIS 8,HYPOTRICHOSIS AND RECURRENT SKIN VESICLES,HYPOTRICHOSIS CONGENITAL WITH JUVENILE MACULAR DYSTROPHY,Hypotrichosis simplex,Hypotrichosis simplex of the scalp,Hypotrichosis simplex of the scalp 2,Hypotrichosis with juvenile macular degeneration,HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME,HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME,HYPOURICEMIA RENAL 1,HYPOURICEMIA RENAL 2,Hypoxanthine guanine phosphoribosyltransferase partial deficiency,ICF syndrome,ichthyosis autosomal recessive with hypotrichosis,ICHTHYOSIS BULLOSA OF SIEMENS,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 1,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 10,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 11,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 12,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 13,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 14,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 2,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 3,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 4A,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 4B,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 5,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 6,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 8,ICHTHYOSIS CONGENITAL AUTOSOMAL RECESSIVE 9,ICHTHYOSIS CYCLIC WITH EPIDERMOLYTIC HYPERKERATOSIS,Ichthyosis follicularis-alopecia-photophobia syndrome,ICHTHYOSIS HYSTRIX CURTH-MACKLIN TYPE,Ichthyosis hystrix of Curth-Macklin,ICHTHYOSIS HYSTRIX-LIKE WITH DEAFNESS,Ichthyosis lamellar 4,ICHTHYOSIS LAMELLAR AUTOSOMAL DOMINANT,ICHTHYOSIS LEUKOCYTE VACUOLES ALOPECIA AND SCLEROSING CHOLANGITIS,ICHTHYOSIS PREMATURITY SYNDROME,Ichthyosis spastic quadriplegia and mental retardation,ICHTHYOSIS VULGARIS,ICHTHYOSIS X-LINKED,Ichthyosis-hypotrichosis syndrome,Ichthyosis-short stature-brachydactyly-microspherophakia syndrome,ICHTHYOTIC KERATODERMA SPASTICITY HYPOMYELINATION AND DYSMORPHIC FACIAL FEATURES,Id macrocephaly and cerebellar hypoplasia,Idiopathic achalasia,Idiopathic aplastic anemia,Idiopathic bronchiectasis,Idiopathic CD4 lymphocytopenia,Idiopathic central precocious puberty,Idiopathic hypercalciuria,Idiopathic juvenile osteoporosis,Idiopathic pulmonary fibrosis,Idiopathic ventricular fibrillation non Brugada type,IFAP SYNDROME 1 WITH OR WITHOUT BRESHECK SYNDROME,IFAP SYNDROME 2,IgA NEPHROPATHY SUSCEPTIBILITY TO 3,IgE RESPONSIVENESS ATOPIC,IL21-related infantile inflammatory bowel disease,IMAGAWA-MATSUMOTO SYNDROME,IMAGe syndrome,Imerslund-Grasbeck syndrome,Imerslund-Grasbeck syndrome 1,IMERSLUND-GRASBECK SYNDROME 2,IMINOGLYCINURIA,IMMUNE DYSREGULATION AND SYSTEMIC HYPERINFLAMMATION SYNDROME,Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome,Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome,Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome,Immune thrombocytopenia,IMMUNODEFICIENCY 10,IMMUNODEFICIENCY 11,IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS,Immunodeficiency 12,Immunodeficiency 13,IMMUNODEFICIENCY 14,IMMUNODEFICIENCY 15A,IMMUNODEFICIENCY 15B,IMMUNODEFICIENCY 16,IMMUNODEFICIENCY 17,IMMUNODEFICIENCY 18,IMMUNODEFICIENCY 19,IMMUNODEFICIENCY 20,IMMUNODEFICIENCY 21,Immunodeficiency 22,IMMUNODEFICIENCY 23,IMMUNODEFICIENCY 24,IMMUNODEFICIENCY 25,Immunodeficiency 26 with or without neurologic abnormalities,IMMUNODEFICIENCY 27A,Immunodeficiency 27b,IMMUNODEFICIENCY 28,Immunodeficiency 29,IMMUNODEFICIENCY 30,IMMUNODEFICIENCY 31A,IMMUNODEFICIENCY 31B,IMMUNODEFICIENCY 31C,IMMUNODEFICIENCY 32A,IMMUNODEFICIENCY 32B,IMMUNODEFICIENCY 33,IMMUNODEFICIENCY 34,IMMUNODEFICIENCY 35,Immunodeficiency 36,IMMUNODEFICIENCY 37,IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION,IMMUNODEFICIENCY 39,IMMUNODEFICIENCY 40,IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY,IMMUNODEFICIENCY 42,IMMUNODEFICIENCY 43,IMMUNODEFICIENCY 44,IMMUNODEFICIENCY 45,Immunodeficiency 46,IMMUNODEFICIENCY 47,IMMUNODEFICIENCY 48,IMMUNODEFICIENCY 49,IMMUNODEFICIENCY 50,IMMUNODEFICIENCY 51,IMMUNODEFICIENCY 52,IMMUNODEFICIENCY 53,IMMUNODEFICIENCY 54,IMMUNODEFICIENCY 55,IMMUNODEFICIENCY 56,IMMUNODEFICIENCY 57 WITH AUTOINFLAMMATION,IMMUNODEFICIENCY 58,IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA,IMMUNODEFICIENCY 60,IMMUNODEFICIENCY 61,IMMUNODEFICIENCY 62,IMMUNODEFICIENCY 63 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY,IMMUNODEFICIENCY 64,IMMUNODEFICIENCY 65 SUSCEPTIBILITY TO VIRAL INFECTIONS,IMMUNODEFICIENCY 66,IMMUNODEFICIENCY 67,IMMUNODEFICIENCY 68,IMMUNODEFICIENCY 69,IMMUNODEFICIENCY 70,IMMUNODEFICIENCY 71 WITH INFLAMMATORY DISEASE AND CONGENITAL THROMBOCYTOPENIA,IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION,IMMUNODEFICIENCY 73A WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LEUKOCYTOSIS,IMMUNODEFICIENCY 73B WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LYMPHOPENIA,IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA,IMMUNODEFICIENCY 74 COVID19-RELATED X-LINKED,IMMUNODEFICIENCY 75,IMMUNODEFICIENCY 76,IMMUNODEFICIENCY 77,IMMUNODEFICIENCY 78 WITH AUTOIMMUNITY AND DEVELOPMENTAL DELAY,IMMUNODEFICIENCY 79,Immunodeficiency 8,IMMUNODEFICIENCY 9,Immunodeficiency by defective expression of MHC class I,Immunodeficiency by defective expression of MHC class II,IMMUNODEFICIENCY COMMON VARIABLE 1,IMMUNODEFICIENCY COMMON VARIABLE 10,IMMUNODEFICIENCY COMMON VARIABLE 11,Immunodeficiency common variable 12,IMMUNODEFICIENCY COMMON VARIABLE 13,IMMUNODEFICIENCY COMMON VARIABLE 14,IMMUNODEFICIENCY COMMON VARIABLE 2,IMMUNODEFICIENCY COMMON VARIABLE 3,IMMUNODEFICIENCY COMMON VARIABLE 4,IMMUNODEFICIENCY COMMON VARIABLE 5,IMMUNODEFICIENCY COMMON VARIABLE 6,IMMUNODEFICIENCY COMMON VARIABLE 7,IMMUNODEFICIENCY COMMON VARIABLE 8 WITH AUTOIMMUNITY,IMMUNODEFICIENCY DEVELOPMENTAL DELAY AND HYPOHOMOCYSTEINEMIA,Immunodeficiency due to a classical component pathway complement deficiency,Immunodeficiency due to a late component of complement deficiency,Immunodeficiency due to CD25 deficiency,IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN,IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY,Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency,Immunodeficiency due to MASP-2 deficiency,IMMUNODEFICIENCY WITH CLEFT LIP/PALATE CATARACT HYPOPIGMENTATION AND ABSENT CORPUS CALLOSUM,Immunodeficiency with factor H anomaly,Immunodeficiency with factor I anomaly,IMMUNODEFICIENCY WITH HYPER-IgM TYPE 1,IMMUNODEFICIENCY WITH HYPER-IgM TYPE 2,IMMUNODEFICIENCY WITH HYPER-IgM TYPE 3,IMMUNODEFICIENCY WITH HYPER-IgM TYPE 5,Immunodeficiency X-Linked with magnesium defect Epstein-Barr virus infection and neoplasia,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4,IMMUNODYSREGULATION POLYENDOCRINOPATHY AND ENTEROPATHY X-LINKED,Immunoglobulin A deficiency 2,Immunoglobulin-mediated membranoproliferative glomerulonephritis,IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES,Impaired Cilia Orientation and Mucociliary Clearance,IMPDH2 ENZYME ACTIVITY VARIATION IN,INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1,Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2,Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3,Inclusion body myopathy with Paget disease of bone and frontotemporal dementia,Incontinentia pigmenti,Increased analgesia from kappa-opioid receptor agonist female-specific,Indifference to pain congenital autosomal recessive,Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy,Infant acute respiratory distress syndrome,Infantile ataxia with oculomotor and pyramidal signs,Infantile Bartter syndrome with sensorineural deafness,INFANTILE CATARACT SKIN ABNORMALITIES GLUTAMATE EXCESS AND IMPAIRED INTELLECTUAL DEVELOPMENT,Infantile cerebellar-retinal degeneration,Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,Infantile convulsions and choreoathetosis,Infantile dystonia-parkinsonism,Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum,Infantile Epilepsy Cataracts and Profound Developmental Delay,INFANTILE EPILEPTIC ENCEPHALOPATHY,INFANTILE EPILEPTIC ENCEPHALOPATHY AND/OR INTELLECTUAL DISABILITY,Infantile epileptic-dyskinetic encephalopathy,Infantile glycine encephalopathy,Infantile hypertrophic cardiomyopathy and lactic acidosis,Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency,Infantile hypertrophic cardiomyopathy lactic acidosis and isolated complex I deficiency,Infantile hypophosphatasia,Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome,Infantile inflammatory bowel disease with neurological involvement,Infantile Krabbe disease,INFANTILE LIVER FAILURE SYNDROME 1,INFANTILE LIVER FAILURE SYNDROME 2,INFANTILE LIVER FAILURE SYNDROME 3,Infantile multisystem neurologic-endocrine-pancreatic disease,Infantile myofibromatosis,Infantile nephronophthisis,INFANTILE NEPHRONOPHTHISIS AND INTELLECTUAL DISABILITY,Infantile nephropathic cystinosis,Infantile neuroaxonal dystrophy,Infantile neuroaxonal dystrophy 1,Infantile onset spinocerebellar ataxia,Infantile osteopetrosis with neuroaxonal dysplasia,Infantile Refsum disease,INFANTILE SIALIC ACID STORAGE DISEASE,Infantile spasms syndrome,Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome,INFANTILE STRIATONIGRAL DEGENERATION,INFANTILE SYSTEMIC HYALINOSIS,Infantile-onset ascending hereditary spastic paralysis,Infantile-onset generalized dyskinesia with orofacial involvement,Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression,Infantile-onset periodic fever-panniculitis-dermatosis syndrome,Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia,Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities,infantile-onset severe developmental delay and skeletal dysplasia,Infantile-onset X-linked spinal muscular atrophy,INFECTIONS RECURRENT WITH ENCEPHALOPATHY HEPATIC DYSFUNCTION AND CARDIOVASCULAR MALFORMATIONS,INFLAMMATORY BOWEL DISEASE 13,INFLAMMATORY BOWEL DISEASE 14,INFLAMMATORY BOWEL DISEASE 17,INFLAMMATORY BOWEL DISEASE 25 AUTOSOMAL RECESSIVE,INFLAMMATORY BOWEL DISEASE 28 AUTOSOMAL RECESSIVE,INFLAMMATORY BOWEL DISEASE 29,INFLAMMATORY BOWEL DISEASE CROHN DISEASE 1,INFLAMMATORY BOWEL DISEASE CROHN DISEASE 10,INFLAMMATORY BOWEL DISEASE CROHN DISEASE 19,INFLAMMATORY BOWEL DISEASE CROHN DISEASE 30,INFLAMMATORY BOWEL DISEASE IMMUNODEFICIENCY AND ENCEPHALOPATHY,Inflammatory bowel disease-recurrent sinopulmonary infections syndrome,Inflammatory myofibroblastic tumor,INFLAMMATORY SKIN AND BOWEL DISEASE NEONATAL 1,INFLAMMATORY SKIN AND BOWEL DISEASE NEONATAL 2,INFLUENZA SEVERE SUSCEPTIBILITY TO,Inherited acute myeloid leukemia,Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations,Inherited congenital spastic tetraplegia,Inherited Creutzfeldt-Jakob disease,Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality,Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency,Inherited Skin Fragility,INOSINE TRIPHOSPHATASE DEFICIENCY,INSENSITIVITY TO PAIN CONGENITAL WITH ANHIDROSIS,INSULIN RECEPTOR SUBSTRATE 1,INSULIN-LIKE GROWTH FACTOR I DEFICIENCY,INSULIN-LIKE GROWTH FACTOR I RESISTANCE TO,INSULIN-LIKE GROWTH FACTOR I RESISTANCE TO biallelic,Insulin-resistance syndrome type A,Insulinoma,INSULINOMATOSIS AND DIABETES MELLITUS,INTELLECTUAL DEVELOPMENTAL DISORDER 59,INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 44 WITH MICROCEPHALY,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 59,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 60 WITH SEIZURES,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 61,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 62,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 63 WITH MACROCEPHALY,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL DOMINANT 64,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 12,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 67,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 68,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 69,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 70,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 71,INTELLECTUAL DEVELOPMENTAL DISORDER AUTOSOMAL RECESSIVE 72,INTELLECTUAL DEVELOPMENTAL DISORDER WITH ABNORMAL BEHAVIOR MICROCEPHALY AND SHORT STATURE,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY WITH OR WITHOUT SEIZURES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA,Intellectual developmental disorder with cardiac defects and dysmorphic facies,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES SEIZURES AND DISTAL LIMB ANOMALIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH EPILEPSY BEHAVIORAL ABNORMALITIES AND COARSE FACIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY SEIZURES AND SPEECH DELAY,INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH DYSMORPHIC FACIES AND VARIABLE SKELETAL ANOMALIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA,INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN,INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE FACIALANOMALIES AND SPEECH DEFECTS,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AND AXONAL PERIPHERAL NEUROPATHY,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AUTISM AND DYSMORPHIC FACIES,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY DYSMORPHIC FACIES AND T-CELL ABNORMALITIES,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED 108,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED 50,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC ARMFIELD TYPE,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC HACKMANN-DI DONATO TYPE,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC LUJAN-FRYNS TYPE,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC RAYMOND TYPE,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC SNIJDERS BLOK TYPE,INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC WU TYPE,Intellectual disability,Intellectual Disability Accompanied by Epilepsy and Autistic Features,Intellectual Disability and Central Nervous System anomalies,Intellectual disability and epilepsy,Intellectual disability and iris abnormalities,Intellectual Disability Ataxia and Facial Dysmorphism,Intellectual disability Birk-Barel type,Intellectual Disability Central Nervous System anomalies and Scoliosis,Intellectual Disability Central Nervous System anomalies and Seizures,Intellectual Disability Congenital Malformations and Failure to Thrive,Intellectual Disability Developmental Delay and Short Stature,Intellectual disability encephalopathy impaired GPI-anchor maturation,Intellectual Disability Seizures Abnormal Gait and Distinctive Facial Features,Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features,Intellectual disability syndrome due to a DYRK1A point mutation,Intellectual disability with ataxia/spasticity,Intellectual disability with autism spectrum disorder,Intellectual Disability with Cerebellar Atrophy,Intellectual disability with epilepsy,Intellectual disability with facial dysmorphism,Intellectual Disability with or without Epileptic Encephalopathy,Intellectual Disability with or without Epileptic Encephalopathy activating,Intellectual disability with pigmentary mosaicism and storage disorder,Intellectual Disability with Seizures,Intellectual Disability with Seizures and Hypotonia,Intellectual Disability with Speech Delay Microcephaly Short Stature and Aggressive Behavior,Intellectual Disability with Variable Brain Anomalies,Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome,Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome,Intellectual disability-cataracts-calcified pinnae-myopathy syndrome,Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome,Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome,Intellectual disability-developmental delay-contractures syndrome,Intellectual disability-epilepsy-extrapyramidal syndrome,Intellectual disability-expressive aphasia-facial dysmorphism syndrome,Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency,Intellectual disability-hyperkinetic movement-truncal ataxia syndrome,Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome,Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome,Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome,Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome,Intellectual disability-severe speech delay-mild dysmorphism syndrome,Intellectual disability-strabismus syndrome,Intellectual disabiltiy,INTERLEUKIN 6 SERUM LEVEL OF QUANTITATIVE TRAIT LOCUS,Intermediate DEND syndrome,Intermediate epidermolysis bullosa simplex with cardiomyopathy,Intermediate generalized junctional epidermolysis bullosa,Intermediate maple syrup urine disease,Intermediate nemaline myopathy,Intermediate osteopetrosis,Intermediate severe Salla disease,Intermittent hydrarthrosis,Intermittent maple syrup urine disease,INTERSTITIAL LUNG AND LIVER DISEASE,Interstitial lung disease due to ABCA3 deficiency,Interstitial lung disease due to SP-C deficiency,Interstitial lung disease nephrotic syndrome and epidermolysis bullosa congenital,Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome,INTERSTITIAL NEPHRITIS KARYOMEGALIC,INTERVERTEBRAL DISC DISEASE,INTESTINAL ATRESIA MULTIPLE,Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency,Intestinal pseudoobstruction neuronal chronic idiopathic X-linked,INTRA-MITOCHONDRIAL METHYLATION DEFICIENCY,Intrahepatic cholestasis of pregnancy,Intraosseous Vascular Malformation,Intrauterine growth restriction-congenital multiple cafe-au-lait macules-increased sister chromatid exchange syndrome,Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome,Intrauterine growth retardation metaphyseal dysplasia adrenal hypoplasia congenita and genital anomalies,INTRAUTERINE GROWTH RETARDATION METAPHYSEAL DYSPLASIA ADRENAL HYPOPLASIA CONGENITA GENITAL ANOMALIES AND IMMUNODEFICIENCY,Intravascular large B-cell lymphoma,INTRINSIC FACTOR DEFICIENCY,IPEX Syndrome,IRIDA syndrome,IRON-REFRACTORY IRON DEFICIENCY ANEMIA,Ischio-vertebral syndrome,ISCHIOCOXOPODOPATELLAR SYNDROME WITH OR WITHOUT PULMONARY ARTERIALHYPERTENSION,ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY,Isolated anencephaly,Isolated aniridia,Isolated Arhinia/Bosma Arhinia syndrome,Isolated asymptomatic elevation of creatine phosphokinase,Isolated ATP synthase deficiency,Isolated autosomal dominant hypomagnesemia Glaudemans type,Isolated Biliary atresia,Isolated bone marrow mastocytosis,Isolated brachycephaly,Isolated cleft lip,Isolated cloverleaf skull syndrome,Isolated complex I deficiency,Isolated complex III deficiency,Isolated congenital adermatoglyphia,Isolated congenital anosmia,Isolated congenital breast hypoplasia/aplasia,Isolated congenital digital clubbing,Isolated congenital megalocornea,Isolated congenital sclerocornea,Isolated congenitally uncorrected transposition of the great arteries,Isolated cytochrome C oxidase deficiency,Isolated Dandy-Walker malformation,Isolated Dandy-Walker malformation with hydrocephalus,Isolated Dandy-Walker malformation without hydrocephalus,Isolated delta-storage pool disease,ISOLATED ECTOPIA LENTIS,Isolated exencephaly,Isolated focal cortical dysplasia type Ia,Isolated focal cortical dysplasia type IIa,Isolated focal cortical dysplasia type IIb,Isolated focal non-epidermolytic palmoplantar keratoderma,Isolated follicle-stimulating hormone deficiency,Isolated generalized anhidrosis with normal sweat glands,Isolated growth hormone deficiency type IA,Isolated growth hormone deficiency type IB,Isolated growth hormone deficiency type II,ISOLATED GROWTH HORMONE DEFICIENCY TYPE III WITH AGAMMAGLOBULINEMIA,ISOLATED GROWTH HORMONE DEFICIENCY TYPE IV,ISOLATED GROWTH HORMONE DEFICIENCY TYPE V,Isolated hemihyperplasia,Isolated hyperchlorhidrosis,Isolated Klippel-Feil syndrome,Isolated megalencephaly,Isolated microphthalmia-anophthalmia-coloboma,Isolated neonatal sclerosing cholangitis,Isolated Nonsyndromic Patent Ductus Arteriosus.,Isolated optic nerve hypoplasia/aplasia,Isolated osteopoikilosis,Isolated oxycephaly,Isolated Pierre Robin syndrome,Isolated plagiocephaly,Isolated polycystic liver disease,Isolated scaphocephaly,Isolated sedoheptulokinase deficiency,Isolated split hand-split foot malformation,Isolated succinate-CoQ reductase deficiency,Isolated sulfite oxidase deficiency,Isolated thyroid-stimulating hormone deficiency,Isolated thyrotropin-releasing hormone deficiency,Isolated trigonocephaly,ISOVALERIC ACIDEMIA,ISPD-related  limb-girdle muscular dystrophy R20,ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement,IVIC SYNDROME,JABERI-ELAHI SYNDROME,JACKSON-WEISS SYNDROME,Jacobsen syndrome,JALILI SYNDROME,JANSEN METAPHYSEAL CHONDRODYSPLASIA,JANSEN-DE VRIES SYNDROME,JARID2-related Neurodevelopmental Disorder,JAWAD SYNDROME,JENSEN SYNDROME,Jervell and Lange-Nielsen syndrome,JERVELL AND LANGE-NIELSEN SYNDROME 1,JERVELL AND LANGE-NIELSEN SYNDROME 2,Jervell and Lange-Nielsen syndrome type 1,Jervell and Lange-Nielsen syndrome type 2,Jeune syndrome,JOHANSON-BLIZZARD SYNDROME,JOINT LAXITY SHORT STATURE AND MYOPIA,Joubert Syndrome,JOUBERT SYNDROME 1,JOUBERT SYNDROME 10,JOUBERT SYNDROME 13,JOUBERT SYNDROME 14,Joubert syndrome 15,JOUBERT SYNDROME 16,JOUBERT SYNDROME 17,JOUBERT SYNDROME 18,Joubert syndrome 2,JOUBERT SYNDROME 20,JOUBERT SYNDROME 21,Joubert syndrome 22,Joubert syndrome 23,Joubert syndrome 24,Joubert syndrome 25,Joubert syndrome 26,JOUBERT SYNDROME 27,JOUBERT SYNDROME 28,JOUBERT SYNDROME 3,Joubert syndrome 30,JOUBERT SYNDROME 31,JOUBERT SYNDROME 32,JOUBERT SYNDROME 33,JOUBERT SYNDROME 35,JOUBERT SYNDROME 36,JOUBERT SYNDROME 37,JOUBERT SYNDROME 4,JOUBERT SYNDROME 5,JOUBERT SYNDROME 6,JOUBERT SYNDROME 7,JOUBERT SYNDROME 8,JOUBERT SYNDROME 9,Joubert Syndrome and Related Disorders,JOUBERT SYNDROME TYPE 1,JOUBERT SYNDROME TYPE 10,JOUBERT SYNDROME TYPE 5,Joubert Syndrome with Cranio-facial and Skeletal Defects,Joubert syndrome with hepatic defect,Joubert syndrome with Jeune asphyxiating thoracic dystrophy,Joubert syndrome with ocular defect,Joubert syndrome with oculorenal defect,Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy,Joubert syndrome with renal defect,Juberg-Hayward syndrome,Junctional epidermolysis bullosa with pyloric atresia,Juvenile absence epilepsy,Juvenile amyotrophic lateral sclerosis,JUVENILE ARTHRITIS,Juvenile cataract-microcornea-renal glucosuria syndrome,Juvenile glaucoma,Juvenile Huntington disease,JUVENILE HYALINE FIBROMATOSIS,Juvenile myelomonocytic leukemia,Juvenile myoclonic epilepsy,Juvenile nephronophthisis,Juvenile nephropathic cystinosis,Juvenile or adult CACH syndrome,Juvenile Paget disease,Juvenile polyposis of infancy,Juvenile polyposis syndrome,Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome,Juvenile primary lateral sclerosis,Juvenile sialidosis type 2,Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome,Kabuki syndrome,KABUKI SYNDROME 1,KABUKI SYNDROME 2,Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation,Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion,Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14,KAHRIZI SYNDROME,KALLIKREIN DECREASED URINARY ACTIVITY OF,Kallmann Syndrome,KANZAKI DISEASE,KAPOSI SARCOMA SUSCEPTIBILITY TO,Kaposiform hemangioendothelioma,Karyomegalic interstitial nephritis,KAT5-related Neurodevelopmental Syndrome,KATNB1- associated COMPLEX CEREBRAL MALFORMATIONS,KAUFMAN OCULOCEREBROFACIAL SYNDROME,KAYA-BARAKAT-MASSON SYNDROME,KBG syndrome,KCN4 related abnormal striatum congenital cataract and intellectual disability.,KCND3-related developmental disorder monoallelic,KCNK3-related developmental disorder monoallelic,KCNQ2-related epileptic encephalopathy,KCNQ3 syndrome,KDELR2-related Osteogenesis Imperfecta,KDM4B-related Developmental Disorder,KDM6B-related developmental disorder monoallelic,KEARNS-SAYRE SYNDROME,Keipert syndrome,Kennedy disease,KENNY-CAFFEY SYNDROME,Kenny-Caffey syndrome type 1,Kenny-Caffey syndrome type 2,Keppen-Lubinsky syndrome,KERATITIS HEREDITARY,KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME AUTOSOMAL DOMINANT,KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME AUTOSOMAL RECESSIVE,KERATOCONUS 1,KERATOCONUS 9,KERATOCONUS WITH CATARACT,Keratoderma hereditarium mutilans,Keratoderma hereditarium mutilans with ichthyosis,KERATODERMA PALMOPLANTAR WITH DEAFNESS,KERATOENDOTHELIITIS FUGAX HEREDITARIA,Keratolytic winter erythema,Keratosis follicularis spinulosa decalvans,KERATOSIS FOLLICULARIS SPINULOSA DECALVANS X-LINKED,KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA,Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome,KERATOSIS PALMOPLANTARIS STRIATA II,KERATOSIS PALMOPLANTARIS STRIATA III,KERATOSIS PILARIS ATROPHICANS,KERATOSIS SEBORRHEIC,Ketoacidosis due to monocarboxylate transporter-1 deficiency,Keutel syndrome,KHAN-KHAN-KATSANIS SYNDROME,KID syndrome,KIDINS220-related Developmental Disorder biallelic,KIF3B-related ciliopathy,KILQUIST SYNDROME,Kindler epidermolysis bullosa,KINDLER SYNDROME,King Denborough syndrome,Kleefstra syndrome,KLEEFSTRA SYNDROME 1,KLEEFSTRA SYNDROME 2,Kleefstra syndrome due to 9q34 microdeletion,Kleefstra syndrome due to a point mutation,KLF7-related developmental disorder,KLHL9-related early-onset distal myopathy,Klippel-Feil Anomaly,Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome,KLIPPEL-FEIL SYNDROME 1 AUTOSOMAL DOMINANT,KLIPPEL-FEIL SYNDROME 2 AUTOSOMAL RECESSIVE,KLIPPEL-FEIL SYNDROME 3 AUTOSOMAL DOMINANT,KLIPPEL-FEIL SYNDROME 4 AUTOSOMAL RECESSIVE WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM,Klippel-Trenaunay syndrome,KMT2D multiple malformations disorder,KMT5B syndrome,KNIEST DYSPLASIA,Knobloch syndrome,KNOBLOCH SYNDROME 1,Knobloch Syndrome Type I,KNOPS BLOOD GROUP SYSTEM,Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome,Kohlschutter-Tonz Syndrome,KOHLSCHUTTER-TONZ SYNDROME-LIKE,Koolen-de Vries syndrome,Koolen-De Vries syndrome due to a point mutation,Kosaki overgrowth syndrome,Kostmann syndrome,KOWARSKI SYNDROME,KRABBE DISEASE,KRABBE DISEASE ATYPICAL DUE TO SAPOSIN A DEFICIENCY,KRT1-related diffuse nonepidermolytic keratoderma,KUFOR-RAKEB SYNDROME,Kuru,KURU SUSCEPTIBILITY TO,Kuskokwim syndrome,Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome,Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency,Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency,Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome,L-2-HYDROXYGLUTARIC ACIDURIA,L-Arginine:glycine amidinotransferase deficiency,L-FERRITIN DEFICIENCY,Lacrimal duct defect,LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME,LACRIMOAURICULODENTODIGITAL SYNDROME,LACTASE DEFICIENCY CONGENITAL,LACTATE DEHYDROGENASE B DEFICIENCY,Lacticacidemia due to PDX1 deficiency,LACTOSE INTOLERANCE ADULT TYPE,LADD SYNDROME,Lafora disease,Laing early-onset distal myopathy,LAMA5-related multisystemic syndrome,Lamb-shaffer syndrome,Lamellar ichthyosis,Laminin subunit alpha 2-related congenital muscular dystrophy,Landau-Kleffner syndrome,LANGER MESOMELIC DYSPLASIA,Langerhans cell histiocytosis,LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA,Large congenital melanocytic nevus,LARON SYNDROME,Laron syndrome with immunodeficiency,LARSEN SYNDROME,Larsen-like syndrome B3GAT3 type,Laryngo-onycho-cutaneous syndrome,LARYNGOONYCHOCUTANEOUS SYNDROME,Late infantile CACH syndrome,Late-infantile/juvenile Krabbe disease,Late-onset distal myopathy Markesbery-Griggs type,Late-onset junctional epidermolysis bullosa,Late-onset nephronophthisis,Late-onset retinal degeneration,Lateral meningocele syndrome,Laterality defects,LATHOSTEROLOSIS,Lattice corneal dystrophy Type I,Laurence-Moon syndrome,Laurin-Sandrow syndrome,Leber congenital amaurosis,LEBER CONGENITAL AMAUROSIS 1,LEBER CONGENITAL AMAUROSIS 10,LEBER CONGENITAL AMAUROSIS 11,LEBER CONGENITAL AMAUROSIS 12,LEBER CONGENITAL AMAUROSIS 13,LEBER CONGENITAL AMAUROSIS 14,LEBER CONGENITAL AMAUROSIS 15,LEBER CONGENITAL AMAUROSIS 16,Leber congenital amaurosis 17,LEBER CONGENITAL AMAUROSIS 19,Leber congenital amaurosis 2,LEBER CONGENITAL AMAUROSIS 3,LEBER CONGENITAL AMAUROSIS 4,LEBER CONGENITAL AMAUROSIS 5,LEBER CONGENITAL AMAUROSIS 6,LEBER CONGENITAL AMAUROSIS 7,LEBER CONGENITAL AMAUROSIS 8,LEBER CONGENITAL AMAUROSIS 9,LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS,Leber hereditary optic neuropathy,LEBER HEREDITARY OPTIC NEUROPATHY MODIFIER OF,LEBER OPTIC ATROPHY,Leber plus disease,LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY,Left ventricular noncompaction,LEFT VENTRICULAR NONCOMPACTION 1,Left ventricular noncompaction 10,LEFT VENTRICULAR NONCOMPACTION 7,LEFT VENTRICULAR NONCOMPACTION 8,LEFT VENTRICULAR OUTFLOW TRACT OBSTRUCTION,Legg-Calve-Perthes disease,LEGIONNAIRE DISEASE SUSCEPTIBILITY TO,LEGIUS SYNDROME,Leigh syndrome,LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY,LEIGH SYNDROME DUP,LEIGH SYNDROME FRENCH CANADIAN TYPE,Leigh syndrome with cardiomyopathy,Leigh Syndrome with Instability of the Small Mitoribosomal Subunit,Leigh syndrome with leukodystrophy,Leigh syndrome with nephrotic syndrome,Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase.,Lennox-Gastaut syndrome,Lenz-Majewski hyperostotic dwarfism,LEOPARD syndrome 1,LEOPARD SYNDROME 2,LEOPARD SYNDROME 3,LEOPARD syndrome type 1,Leprechaunism,LEPROSY SUSCEPTIBILITY TO 3,LEPROSY SUSCEPTIBILITY TO 4,LEPROSY SUSCEPTIBILITY TO 5,LEPTIN DEFICIENCY OR DYSFUNCTION,LEPTIN RECEPTOR DEFICIENCY,Leri-Weill dyschondrosteosis,LESCH-NYHAN SYNDROME,LESSEL-KREIENKAMP SYNDROME,LESSEL-KUBISCH SYNDROME,Lethal acantholytic erosive disorder,Lethal arteriopathy syndrome due to Fibulin-4 deficiency,Lethal arthroogryposis,Lethal ataxia with deafness and optic atrophy,Lethal brain and heart developmental defects,LETHAL CONGENITAL CONTRACTURE SYNDROME 1,LETHAL CONGENITAL CONTRACTURE SYNDROME 10,LETHAL CONGENITAL CONTRACTURE SYNDROME 11,LETHAL CONGENITAL CONTRACTURE SYNDROME 2,LETHAL CONGENITAL CONTRACTURE SYNDROME 3,LETHAL CONGENITAL CONTRACTURE SYNDROME 4,Lethal congenital contracture syndrome 5,Lethal congenital contracture syndrome 6,LETHAL CONGENITAL CONTRACTURE SYNDROME 7,LETHAL CONGENITAL CONTRACTURE SYNDROME 8,LETHAL CONGENITAL CONTRACTURE SYNDROME 9,Lethal congenital contracture syndrome type 1,lethal congenital contracture syndrome type 2,lethal congenital contracture syndrome type 3,Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome,Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome,Lethal hydranencephaly-diaphragmatic hernia syndrome,Lethal Infantile Epileptic Encephalopathy,Lethal infantile mitochondrial myopathy,Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome,Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome,Lethal multiple pterygium syndrome,Lethal neonatal rigidity and seizure syndrome,Lethal neonatal spasticity-epileptic encephalopathy syndrome,Lethal Neurometabolic Disorder of Early Childhood,Lethal occipital encephalocele-skeletal dysplasia syndrome,Lethal osteosclerotic bone dysplasia,Lethal polymalformative syndrome Boissel type,Lethal Restrictive Dermopathy ZMPSTE24-Related,Letrozole toxicity,LEUKEMIA ACUTE LYMPHOBLASTIC,Leukemia acute lymphoblastic susceptibility to 3,LEUKEMIA ACUTE MYELOID,LEUKEMIA CHRONIC MYELOID,Leukocyte adhesion deficiency type I,Leukocyte adhesion deficiency type II,Leukocyte adhesion deficiency type III,LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA,LEUKODYSTROPHY DEMYELINATING ADULT-ONSET AUTOSOMAL DOMINANT,LEUKODYSTROPHY HYPOMYELINATING 10,LEUKODYSTROPHY HYPOMYELINATING 11,Leukodystrophy hypomyelinating 12,LEUKODYSTROPHY HYPOMYELINATING 13,LEUKODYSTROPHY HYPOMYELINATING 14,LEUKODYSTROPHY HYPOMYELINATING 15,LEUKODYSTROPHY HYPOMYELINATING 16,LEUKODYSTROPHY HYPOMYELINATING 17,LEUKODYSTROPHY HYPOMYELINATING 18,LEUKODYSTROPHY HYPOMYELINATING 19 TRANSIENT INFANTILE,LEUKODYSTROPHY HYPOMYELINATING 2,LEUKODYSTROPHY HYPOMYELINATING 20,LEUKODYSTROPHY HYPOMYELINATING 3,LEUKODYSTROPHY HYPOMYELINATING 4,LEUKODYSTROPHY HYPOMYELINATING 5,LEUKODYSTROPHY HYPOMYELINATING 6,LEUKODYSTROPHY HYPOMYELINATING 7 WITH OR WITHOUT OLIGODONTIAAND/OR HYPOGONADOTROPIC HYPOGONADISM,LEUKODYSTROPHY HYPOMYELINATING 8 WITH OR WITHOUT OLIGODONTIAAND/OR HYPOGONADOTROPIC HYPOGONADISM,LEUKODYSTROPHY HYPOMYELINATING 9,LEUKODYSTROPHY HYPOMYELINATING TYPE 1,LEUKODYSTROPHY HYPOMYELINATING TYPE 4,LEUKODYSTROPHY HYPOMYELINATING TYPE 5,LEUKODYSTROPHY PROGRESSIVE EARLY CHILDHOOD-ONSET,LEUKOENCEPHALOPATHY ACUTE REVERSIBLE WITH INCREASED URINARY ALPHA-KETOGLUTARATE,LEUKOENCEPHALOPATHY BRAIN CALCIFICATIONS AND CYSTS,LEUKOENCEPHALOPATHY CYSTIC WITHOUT MEGALENCEPHALY,LEUKOENCEPHALOPATHY DEVELOPMENTAL DELAY AND EPISODIC NEUROLOGIC REGRESSION SYNDROME,LEUKOENCEPHALOPATHY HEREDITARY DIFFUSE WITH SPHEROIDS,LEUKOENCEPHALOPATHY MEGALENCEPHALIC WITH SUBCORTICAL CYSTS,LEUKOENCEPHALOPATHY MOTOR DELAY SPASTICITY AND DYSARTHRIA SYNDROME,LEUKOENCEPHALOPATHY PROGRESSIVE INFANTILE-ONSET WITH OR WITHOUT DEAFNESS,LEUKOENCEPHALOPATHY PROGRESSIVE WITH OVARIAN FAILURE,LEUKOENCEPHALOPATHY WITH ATAXIA,Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome,LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION,Leukoencephalopathy with calcifications and cysts,Leukoencephalopathy with cerebral calcification and cysts,LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY,Leukoencephalopathy with mild cerebellar ataxia and white matter edema,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER,Leukoencephalopathy-dystonia-motor neuropathy syndrome,Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome,Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome,Leukonychia totalis,LEUKOTRIENE C4 SYNTHASE DEFICIENCY,Leydig cell hypoplasia due to complete LH resistance,Leydig cell hypoplasia due to LHB deficiency,Leydig cell hypoplasia due to partial LH resistance,LEYDIG CELL HYPOPLASIA TYPE I,LHERMITTE-DUCLOS DISEASE,LHX4-Related Combined Pituitary Hormone Deficiency,LI-CAMPEAU SYNDROME,Li-Fraumeni syndrome,LI-FRAUMENI SYNDROME 2,LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME,LIANG-WANG SYNDROME,LIBERFARB SYNDROME,Lichtenstein-Knorr syndrome,LIDDLE SYNDROME,LIDDLE SYNDROME 1,LIDDLE SYNDROME 2,LIDDLE SYNDROME 3,LIEBENBERG SYNDROME,LIG4 SYNDROME,Limb-girdle muscular dystrophy due to POMK deficiency,LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2H,LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2L,LIMB-MAMMARY SYNDROME,Limbic encephalitis with LGI1 antibodies,Limited cutaneous systemic sclerosis,Limited systemic sclerosis,LIMS2-related limb-girdle muscular dystrophy,Linear nevus sebaceus syndrome,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 1,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3,LINGO1 related intellectual disability with microcephaly speech and motor delay,Lipase deficiency combined,LIPE-related familial partial lipodystrophy,LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY,LIPODYSTROPHY CONGENITAL GENERALIZED TYPE 1,LIPODYSTROPHY CONGENITAL GENERALIZED TYPE 2,LIPODYSTROPHY CONGENITAL GENERALIZED TYPE 3,LIPODYSTROPHY CONGENITAL GENERALIZED TYPE 4,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 2,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 3,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 4,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 5,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 6,LIPODYSTROPHY FAMILIAL PARTIAL TYPE 7,LIPODYSTROPHY PARTIAL ACQUIRED SUSCEPTIBILITY TO,Lipoic acid synthetase deficiency,LIPOID CONGENITAL ADRENAL HYPERPLASIA,Lipoid proteinosis,LIPOID PROTEINOSIS OF URBACH AND WIETHE,LIPOPROTEIN GLOMERULOPATHY,LIPOPROTEINa QUANTITATIVE TRAIT LOCUS,Lipoyl transferase 2 deficiency,LIPOYLTRANSFERASE 1 DEFICIENCY,LISSENCEPHALY 1,LISSENCEPHALY 10,Lissencephaly 2,LISSENCEPHALY 3,Lissencephaly 4,LISSENCEPHALY 5,Lissencephaly 6 with microcephaly,LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA,LISSENCEPHALY 8,LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION,Lissencephaly due to LIS1 mutation,Lissencephaly due to TUBA1A mutation,Lissencephaly Subcortical Heterotopia and Global Developmental Delay,Lissencephaly syndrome Norman-Roberts type,LISSENCEPHALY TYPE 1,Lissencephaly type 1 due to doublecortin gene mutation,LISSENCEPHALY TYPE 3,LISSENCEPHALY X-LINKED 1,LISSENCEPHALY X-LINKED 2,LISSENCEPHALY X-LINKED TYPE 1,LIVER FAILURE INFANTILE TRANSIENT,LMNA-related cardiocutaneous progeria syndrome,LMNB1-associated developmental disorder,LMNB2-related Primary Microcephaly,Lobar holoprosencephaly,Localized dystrophic epidermolysis bullosa acral form,Localized dystrophic epidermolysis bullosa nails only,Localized dystrophic epidermolysis bullosa pretibial form,Localized epidermolysis bullosa simplex,Localized junctional epidermolysis bullosa,Loeys-Dietz syndrome,LOEYS-DIETZ SYNDROME 1,LOEYS-DIETZ SYNDROME 2,LOEYS-DIETZ SYNDROME 3,LOEYS-DIETZ SYNDROME 4,LOEYS-DIETZ SYNDROME 5,LOEYS-DIETZ SYNDROME TYPE 4,Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,LONG QT SYNDROME 1,LONG QT SYNDROME 10,LONG QT SYNDROME 11,LONG QT SYNDROME 12,Long QT syndrome 13,LONG QT SYNDROME 14,LONG QT SYNDROME 15,LONG QT SYNDROME 16,LONG QT SYNDROME 2,LONG QT SYNDROME 3,LONG QT SYNDROME 5,LONG QT SYNDROME 6,Long QT syndrome 8,LONG QT SYNDROME 9,LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY,LOPES-MACIEL-RODAN SYNDROME,Low density lipoprotein cholesterol level quantitative trait locus 6,LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 7,LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 8,Low isolated anorectal malformation,Low phospholipid associated cholelithiasis,LOWE OCULOCEREBRORENAL SYNDROME,Lower motor neuron syndrome with late-adult onset,LOWER URINARY TRACT OBSTRUCTION CONGENITAL,Lowry-Wood syndrome,LRP5-related primary osteoporosis,LUBS X-LINKED MENTAL RETARDATION SYNDROME,LUJAN-FRYNS SYNDROME,Lumbosacral spina bifida aperta,Lumbosacral spina bifida cystica,LUNG CANCER ALVEOLAR CELL CARCINOMA INCLUDED,LUNG DISEASE IMMUNODEFICIENCY AND CHROMOSOME BREAKAGE SYNDROME,LUSCAN-LUMISH SYNDROME,LUTHERAN NULL,LYMPHANGIOLEIOMYOMATOSIS,LYMPHATIC MALFORMATION 1,LYMPHATIC MALFORMATION 3,LYMPHATIC MALFORMATION 4,LYMPHATIC MALFORMATION 6,LYMPHATIC MALFORMATION 7,LYMPHATIC MALFORMATION 8,Lymphedema hereditary ic,LYMPHEDEMA PRIMARY WITH MYELODYSPLASIA,LYMPHEDEMA-DISTICHIASIS SYNDROME,Lymphedema-posterior choanal atresia syndrome,LYMPHOID ENHANCER-BINDING FACTOR 1,LYMPHOMA HODGKIN CLASSIC,LYMPHOMA MUCOSA-ASSOCIATED LYMPHOID TYPE,LYMPHOMA NON-HODGKIN FAMILIAL,Lymphomatoid papulosis,LYMPHOPROLIFERATIVE SYNDROME 1,LYMPHOPROLIFERATIVE SYNDROME 2,LYMPHOPROLIFERATIVE SYNDROME 3,LYMPHOPROLIFERATIVE SYNDROME X-LINKED 1,LYMPHOPROLIFERATIVE SYNDROME X-LINKED 2,Lynch syndrome,Lynch syndrome I,LYSINURIC PROTEIN INTOLERANCE,Lysosomal acid lipase deficiency,LYSOSOMAL ALPHA-MANNOSIDOSIS,LYSOSOMAL BETA-MANNOSIDOSIS,LYSYL HYDROXYLASE 3 DEFICIENCY,MACHADO-JOSEPH DISEASE,Machado-Joseph disease type 1,Machado-Joseph disease type 2,Machado-Joseph disease type 3,MACROCEPHALY ACQUIRED WITH IMPAIRED INTELLECTUAL DEVELOPMENT,MACROCEPHALY ALOPECIA CUTIS LAXA AND SCOLIOSIS TALL FOREHEAD SPARSE HAIR SKIN HYPEREXTENSIBILITY AND SCOLIOSIS,Macrocephaly and impaired speech and language,MACROCEPHALY DYSMORPHIC FACIES AND PSYCHOMOTOR RETARDATION,Macrocephaly macrosomia facial dysmorphism syndrome,Macrocephaly Neurodevelopmental Delay and Seizures,Macrocephaly with intellectual disability,Macrocephaly-developmental delay syndrome,Macrocephaly-intellectual disability-autism syndrome,Macrocephaly-intellectual disability-left ventricular non compaction syndrome,Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome,MACROCEPHALY/AUTISM SYNDROME,Macrocephaly/megalencephaly syndrome autosomal recessive,MACRODACTYLY,Macrodactyly of fingers unilateral,Macrodactyly of toes unilateral,MACROGLOBULINEMIA WALDENSTROM SUSCEPTIBILITY TO 1,Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss,MACROTHROMBOCYTOPENIA AUTOSOMAL DOMINANT TUBB1-RELATED,Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome,MACS syndrome,Macular corneal dystrophy,MACULAR DEGENERATION AGE-RELATED 1,MACULAR DEGENERATION AGE-RELATED 11,MACULAR DEGENERATION AGE-RELATED 12,MACULAR DEGENERATION AGE-RELATED 13,MACULAR DEGENERATION AGE-RELATED 14,MACULAR DEGENERATION AGE-RELATED 15,MACULAR DEGENERATION AGE-RELATED 2,MACULAR DEGENERATION AGE-RELATED 4,MACULAR DEGENERATION AGE-RELATED 5,MACULAR DEGENERATION AGE-RELATED 6,MACULAR DEGENERATION AGE-RELATED 7,MACULAR DEGENERATION AGE-RELATED 8,MACULAR DEGENERATION AGE-RELATED 9,MACULAR DEGENERATION EARLY-ONSET,MACULAR DEGENERATION X-LINKED ATROPHIC,MACULAR DYSTROPHY CORNEAL,MACULAR DYSTROPHY PATTERNED 1,MACULAR DYSTROPHY PATTERNED 2,MACULAR DYSTROPHY PATTERNED 3,MACULAR DYSTROPHY RETINAL 2,MACULAR DYSTROPHY VITELLIFORM 2,MACULAR DYSTROPHY VITELLIFORM 4,MACULAR DYSTROPHY VITELLIFORM 5,MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT,MADD-related developmental disorder,Maffucci syndrome,MAGEL2-related Prader-Willi-like syndrome,Mainzer-Saldino Syndrome,MAJEED SYNDROME,MAJOR AFFECTIVE DISORDER 7,MAJOR DEPRESSIVE DISORDER,MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I B,MAL DE MELEDA,Malan overgrowth syndrome,MALARIA MILD SUSCEPTIBILITY TO,MALARIA SUSCEPTIBILITY TO MALARIA RESISTANCE TO INCLUDED,Malate-Aspartate Shuttle-Related Encephalopathy,Male infertility due to acephalic spermatozoa,Male infertility due to globozoospermia,Male infertility due to large-headed multiflagellar polyploid spermatozoa,Male infertility with azoospermia or oligozoospermia due to single gene mutation,Male infertility with teratozoospermia due to single gene mutation,MALEYLACETOACETATE ISOMERASE DEFICIENCY,Malformations of cortical development and microcephaly.,Maligant granulosa cell tumor of the ovary,Malignant epithelial tumor of salivary glands,Malignant hyperthermia of anesthesia,MALIGNANT HYPERTHERMIA SUSCEPTIBILITY TO 1,MALIGNANT HYPERTHERMIA SUSCEPTIBILITY TO 5,Malignant migrating focal seizures of infancy,Malignant migrating partial seizures of infancy,Malignant peripheral nerve sheath tumor,Malignant Sertoli-Leydig cell tumor of the ovary,Malonic aciduria,MALONYL-CoA DECARBOXYLASE DEFICIENCY,MALT lymphoma,MAN1B1-CDG,Mandibular hypoplasia deafness progeroid features and lipodystrophy syndrome,Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome,MANDIBULOACRAL DYSPLASIA PROGEROID SYNDROME,MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY,MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY,MANDIBULOFACIAL DYSOSTOSIS GUION-ALMEIDA TYPE,MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA,MANDIBULOFACIAL DYSOSTOSIS WITH MICROCEPHALY,Mandibulofacial dysostosis-microcephaly syndrome,Manitoba oculotrichoanal syndrome,MANNOSE-BINDING LECTIN DEFICIENCY,MANNOSIDOSIS ALPHA B LYSOSOMAL,MANNOSIDOSIS BETA A LYSOSOMAL,MANTLE CELL LYMPHOMA,MAPK1-related Neurodevelopmental Disorder,MAPKAPK5-associated syndrome with synpolydactyly,Maple Syrup Urine Disease,MAPLE SYRUP URINE DISEASE MILD VARIANT,Marden-Walker syndrome,Marfan Syndrome,Marfan syndrome type 1,Marfan syndrome type 2,Marfanoid Habitus and Cognitive Impairment,MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME,Marie Unna hereditary hypotrichosis,MARINESCO-SJOEGREN SYNDROME,Marinesco-Sjogren syndrome,MARSHALL SYNDROME,MARSHALL-SMITH SYNDROME,MARSILI SYNDROME,Martinez-Frias syndrome,Martinique crinkled retinal pigment epitheliopathy,MARTSOLF SYNDROME,MASA SYNDROME,MASP2 DEFICIENCY,MASS syndrome,MAST SYNDROME,MAST1-related developmental disorder monoallelic,MASTOCYTOSIS CUTANEOUS,Maternal phenylketonuria,Maternal riboflavin deficiency,Maternally inherited diabetes and deafness,Matthew-Wood syndrome,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 1,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 10,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 11,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 13,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 14,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 2,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 3,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 4,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 6,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 7,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 8 WITH EXOCRINE DYSFUNCTION,MATURITY-ONSET DIABETES OF THE YOUNG TYPE 9,MAU2 neurodevelopmental disorder,Mazabraud syndrome,McCune-Albright syndrome,McKusick-Kaufman syndrome,McLeod neuroacanthocytosis syndrome,MCLEOD SYNDROME,MCT8 (SLC16A2)-Specific Thyroid Hormone Cell Transporter Deficiency,MEACHAM SYNDROME,Meckel syndrome,Meckel syndrome 12,Meckel syndrome 13,Meckel syndrome 9,MECKEL SYNDROME TYPE 1,MECKEL SYNDROME TYPE 10,Meckel syndrome type 11,MECKEL SYNDROME TYPE 2,MECKEL SYNDROME TYPE 3,MECKEL SYNDROME TYPE 4,MECKEL SYNDROME TYPE 5,MECKEL SYNDROME TYPE 6,MECKEL SYNDROME TYPE 7,MECKEL SYNDROME TYPE 8,MECKEL SYNDROME TYPE 9,Meconium Ileus,MED12-related Developmental Disorder,MED13 - Neurodevelopment disorder,MED27-related neurodevelopmental disorder,Medium chain acyl-CoA dehydrogenase deficiency,Medium-chain acyl-coenzyme A dehydrogenase deficiency,MEDNIK syndrome,MEDNIK-like Syndrome,Medullary sponge kidney,Medulloblastoma,Medulloblastoma with extensive nodularity,MEESMANN CORNEAL DYSTROPHY,MEESTER-LOEYS SYNDROME,MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS,MEGABLADDER CONGENITAL,Megaconial congenital muscular dystrophy,Megacystis-microcolon-intestinal hypoperistalsis syndrome,Megakaryoblastic acute myeloid leukemia with t1,Megalencephalic leukoencephalopathy with subcortical cysts,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A,Megalencephalic leukoencephalopathy with subcortical cysts 2b remitting with or without mental retardation,Megalencephaly-capillary malformation-polymicrogyria syndrome,Megalencephaly-Capillary malformation-Polymicrogyria syndrome somatic  3,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2,Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3,Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome,Megalencephaly-severe kyphoscoliosis-overgrowth syndrome,Megaloblastic anemia due to dihydrofolate reductase deficiency,MEGALOCORNEA,Megalocornea X-linked,MEGDEL syndrome,MEHMO syndrome,Meier-Gorlin syndrome 1,Meier-Gorlin syndrome 2,Meier-Gorlin syndrome 3,Meier-Gorlin syndrome 4,Meier-Gorlin syndrome 5,MEIER-GORLIN SYNDROME 6,MEIER-GORLIN SYNDROME 7,MEIER-GORLIN SYNDROME 8,Meier-Gorlin Syndrome and Craniosynostosis,MEIS2-related developmental disorder monoallelic,Melanocytic nevus syndrome congenital,Melanoma and neural system tumor syndrome,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 1,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 10,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 2,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 3,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 5,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 6,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 8,MELANOMA CUTANEOUS MALIGNANT SUSCEPTIBILITY TO 9,Melanoma of soft tissue,MELANOMA-ASTROCYTOMA SYNDROME,Melanoma-pancreatic cancer syndrome,Melanosis neurocutaneous,MELAS,MELIOIDOSIS SUSCEPTIBILITY TOMELIOIDOSIS RESISTANCE TO INCLUDED,MELNICK-NEEDLES SYNDROME,MELORHEOSTOSIS ISOLATED,Melorheostosis with osteopoikilosis,MEMORY QUANTITATIVE TRAIT LOCUS,MEND syndrome,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency,Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency,Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency,Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency,Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency,Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency,Meningioma,MENINGIOMA FAMILIAL SUSCEPTIBILITY TO,Menke-Hennekam syndrome 1,MENKE-HENNEKAM SYNDROME 2,MENKES DISEASE,Menstrual cycle-dependent periodic fever,Mental retardation and distinctive facial features with or without cardiac defects,Mental retardation and microcephaly with pontine and cerebellar hypoplasia,Mental retardation anterior maxillary protrusion and strabismus,Mental retardation autosomal dominant 1,MENTAL RETARDATION AUTOSOMAL DOMINANT 10,MENTAL RETARDATION AUTOSOMAL DOMINANT 11,MENTAL RETARDATION AUTOSOMAL DOMINANT 13,MENTAL RETARDATION AUTOSOMAL DOMINANT 19,MENTAL RETARDATION AUTOSOMAL DOMINANT 20,MENTAL RETARDATION AUTOSOMAL DOMINANT 21,Mental retardation autosomal dominant 22,Mental retardation autosomal dominant 23,Mental retardation autosomal dominant 24,MENTAL RETARDATION AUTOSOMAL DOMINANT 26,MENTAL RETARDATION AUTOSOMAL DOMINANT 27,MENTAL RETARDATION AUTOSOMAL DOMINANT 28,MENTAL RETARDATION AUTOSOMAL DOMINANT 29,MENTAL RETARDATION AUTOSOMAL DOMINANT 3,MENTAL RETARDATION AUTOSOMAL DOMINANT 30,Mental retardation autosomal dominant 31,MENTAL RETARDATION AUTOSOMAL DOMINANT 32,MENTAL RETARDATION AUTOSOMAL DOMINANT 33,MENTAL RETARDATION AUTOSOMAL DOMINANT 34,MENTAL RETARDATION AUTOSOMAL DOMINANT 35,MENTAL RETARDATION AUTOSOMAL DOMINANT 36,MENTAL RETARDATION AUTOSOMAL DOMINANT 38,Mental retardation autosomal dominant 39,MENTAL RETARDATION AUTOSOMAL DOMINANT 40,MENTAL RETARDATION AUTOSOMAL DOMINANT 41,MENTAL RETARDATION AUTOSOMAL DOMINANT 42,MENTAL RETARDATION AUTOSOMAL DOMINANT 43,MENTAL RETARDATION AUTOSOMAL DOMINANT 45,MENTAL RETARDATION AUTOSOMAL DOMINANT 46,MENTAL RETARDATION AUTOSOMAL DOMINANT 47,MENTAL RETARDATION AUTOSOMAL DOMINANT 48,MENTAL RETARDATION AUTOSOMAL DOMINANT 5,MENTAL RETARDATION AUTOSOMAL DOMINANT 50,MENTAL RETARDATION AUTOSOMAL DOMINANT 51,MENTAL RETARDATION AUTOSOMAL DOMINANT 52,MENTAL RETARDATION AUTOSOMAL DOMINANT 53,MENTAL RETARDATION AUTOSOMAL DOMINANT 54,MENTAL RETARDATION AUTOSOMAL DOMINANT 55 WITH SEIZURES,MENTAL RETARDATION AUTOSOMAL DOMINANT 56,MENTAL RETARDATION AUTOSOMAL DOMINANT 57,MENTAL RETARDATION AUTOSOMAL DOMINANT 58,MENTAL RETARDATION AUTOSOMAL DOMINANT 6,MENTAL RETARDATION AUTOSOMAL DOMINANT 6 WITH OR WITHOUT SEIZURES,MENTAL RETARDATION AUTOSOMAL DOMINANT 7,MENTAL RETARDATION AUTOSOMAL DOMINANT TYPE 3,MENTAL RETARDATION AUTOSOMAL DOMINANT TYPE 4,MENTAL RETARDATION AUTOSOMAL DOMINANT TYPE 5,mental retardation autosomal dominant type 7,Mental retardation autosomal recessive 1,MENTAL RETARDATION AUTOSOMAL RECESSIVE 12,MENTAL RETARDATION AUTOSOMAL RECESSIVE 13,MENTAL RETARDATION AUTOSOMAL RECESSIVE 14,MENTAL RETARDATION AUTOSOMAL RECESSIVE 18,MENTAL RETARDATION AUTOSOMAL RECESSIVE 2,Mental retardation autosomal recessive 27,MENTAL RETARDATION AUTOSOMAL RECESSIVE 3,MENTAL RETARDATION AUTOSOMAL RECESSIVE 34 WITH VARIANT LISSENCEPHALY,Mental retardation autosomal recessive 36,MENTAL RETARDATION AUTOSOMAL RECESSIVE 37,Mental retardation autosomal recessive 38,Mental retardation autosomal recessive 39,Mental retardation autosomal recessive 40,MENTAL RETARDATION AUTOSOMAL RECESSIVE 41,Mental retardation autosomal recessive 42,Mental retardation autosomal recessive 43,Mental retardation autosomal recessive 44,Mental retardation autosomal recessive 45,Mental retardation autosomal recessive 46,Mental retardation autosomal recessive 47,MENTAL RETARDATION AUTOSOMAL RECESSIVE 48,MENTAL RETARDATION AUTOSOMAL RECESSIVE 5,MENTAL RETARDATION AUTOSOMAL RECESSIVE 50,Mental retardation autosomal recessive 51,MENTAL RETARDATION AUTOSOMAL RECESSIVE 52,MENTAL RETARDATION AUTOSOMAL RECESSIVE 53,MENTAL RETARDATION AUTOSOMAL RECESSIVE 54,MENTAL RETARDATION AUTOSOMAL RECESSIVE 56,MENTAL RETARDATION AUTOSOMAL RECESSIVE 57,MENTAL RETARDATION AUTOSOMAL RECESSIVE 58,MENTAL RETARDATION AUTOSOMAL RECESSIVE 59,MENTAL RETARDATION AUTOSOMAL RECESSIVE 6,MENTAL RETARDATION AUTOSOMAL RECESSIVE 60,MENTAL RETARDATION AUTOSOMAL RECESSIVE 61,MENTAL RETARDATION AUTOSOMAL RECESSIVE 63,MENTAL RETARDATION AUTOSOMAL RECESSIVE 64,MENTAL RETARDATION AUTOSOMAL RECESSIVE 65,MENTAL RETARDATION AUTOSOMAL RECESSIVE 66,MENTAL RETARDATION AUTOSOMAL RECESSIVE 7,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 1,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 13,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 18,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 2A,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 3,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 6,MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 7,MENTAL RETARDATION ENTEROPATHY DEAFNESS PERIPHERAL NEUROPATHY ICHTHYOSIS AND KERATODERMA,MENTAL RETARDATION FRA12A TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED CABEZAS TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED CHRISTIANSON TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED JARID1C-RELATED,MENTAL RETARDATION SYNDROMIC X-LINKED LUBS TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED SIDERIUS TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED TURNER TYPE,MENTAL RETARDATION SYNDROMIC X-LINKED TYPE 10,MENTAL RETARDATION SYNDROMIC X-LINKED TYPE 14,MENTAL RETARDATION SYNDROMIC X-LINKED ZDHHC9-RELATED,MENTAL RETARDATION TRUNCAL OBESITY RETINAL DYSTROPHY AND MICROPENISSYNDROME,Mental retardation with language impairment and autistic features,MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES,MENTAL RETARDATION X-LINKED 1,Mental retardation X-linked 100,Mental retardation X-linked 101,MENTAL RETARDATION X-LINKED 102,MENTAL RETARDATION X-LINKED 103,MENTAL RETARDATION X-LINKED 104,MENTAL RETARDATION X-LINKED 105,MENTAL RETARDATION X-LINKED 106,MENTAL RETARDATION X-LINKED 107,MENTAL RETARDATION X-LINKED 12,MENTAL RETARDATION X-LINKED 19,MENTAL RETARDATION X-LINKED 21,MENTAL RETARDATION X-LINKED 3,MENTAL RETARDATION X-LINKED 30,MENTAL RETARDATION X-LINKED 41,MENTAL RETARDATION X-LINKED 58,MENTAL RETARDATION X-LINKED 63,MENTAL RETARDATION X-LINKED 72,MENTAL RETARDATION X-LINKED 9,MENTAL RETARDATION X-LINKED 90,MENTAL RETARDATION X-LINKED 93,MENTAL RETARDATION X-LINKED 96,MENTAL RETARDATION X-LINKED 97,Mental retardation X-linked 98,Mental retardation X-linked 99,MENTAL RETARDATION X-LINKED 99 SYNDROMIC FEMALE-RESTRICTED,MENTAL RETARDATION X-LINKED ARX-RELATED,MENTAL RETARDATION X-LINKED ASSOCIATED WITH FRAGILE SITE FRAXE,MENTAL RETARDATION X-LINKED CASK-RELATED,MENTAL RETARDATION X-LINKED OPHN1-RELATED,MENTAL RETARDATION X-LINKED SYNDROMIC 11,MENTAL RETARDATION X-LINKED SYNDROMIC 13,MENTAL RETARDATION X-LINKED SYNDROMIC 14,MENTAL RETARDATION X-LINKED SYNDROMIC 32,Mental retardation X-linked syndromic 33,MENTAL RETARDATION X-LINKED SYNDROMIC 34,MENTAL RETARDATION X-LINKED SYNDROMIC 35,MENTAL RETARDATION X-LINKED SYNDROMIC BAIN TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC CABEZAS TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC CHRISTIANSON TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC CLAES-JENSEN TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC HEDERA TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC HOUGE TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC NASCIMENTO TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC SNYDER-ROBINSON TYPE,MENTAL RETARDATION X-LINKED SYNDROMIC TURNER TYPE,MENTAL RETARDATION X-LINKED SYP-RELATED,MENTAL RETARDATION X-LINKED TYPE 1,MENTAL RETARDATION X-LINKED TYPE 21,MENTAL RETARDATION X-LINKED TYPE 30,MENTAL RETARDATION X-LINKED TYPE 41,MENTAL RETARDATION X-LINKED TYPE 44,MENTAL RETARDATION X-LINKED TYPE 46,mental retardation X-linked type 58,MENTAL RETARDATION X-LINKED TYPE 59,MENTAL RETARDATION X-LINKED TYPE 63,Mental retardation x-Linked type 72 (MRX72) +/- parkinsons,MENTAL RETARDATION X-LINKED TYPE 90,MENTAL RETARDATION X-LINKED TYPE 91,MENTAL RETARDATION X-LINKED TYPE 93,MENTAL RETARDATION X-LINKED TYPE 94,MENTAL RETARDATION X-LINKED TYPE 95,MENTAL RETARDATION X-LINKED WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE,MENTAL RETARDATION X-LINKED WITH EPILEPSY,MENTAL RETARDATION X-LINKED WITH ISOLATED GROWTH HORMONE DEFICIENCY,MENTAL RETARDATION X-LINKED WITH OR WITHOUT SEIZURES ARX-RELATED,MENTAL RETARDATION X-LINKED WITH PANHYPOPITUITARISM MENTAL RETARDATION X-LINKED WITH ISOLATED GROWTH HORMONE DEFICIENCY INCLUDED,MENTAL RETARDATION X-LINKED ZNF711-RELATED,MENTAL RETARDATION-ANTERIOR MAXILLARY PROTRUSION-STRABISMUS,MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME X-LINKED 1,MENTAL RETARDATION-JOINT HYPERMOBILITY-SKIN LAXITY WITH OR WITHOUT METABOLIC ABNORMALITIES,MENTAL RETARDATION-STEREOTYPIC MOVEMENTS-EPILEPSY AND/OR CEREBRAL MALFORMATIONS,MENTAL RETARDATION-TRUNCAL OBESITY-RETINAL DYSTROPHY-MICROPENIS,MEPAN syndrome,MERRF,Mesoaxial synostotic syndactyly with phalangeal reduction,Mesoaxial synostotic syndactyly with phalangeal reduction malik-Percin type,MESOTHELIOMA MALIGNANT,METABOLIC CRISES RECURRENT WITH RHABDOMYOLYSIS CARDIAC ARRHYTHMIAS AND NEURODEGENERATION,METABOLIC CRISES RECURRENT WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION,Metabolic myopathy due to lactate transporter defect,METACARPAL 4-5 FUSION,Metachondromatosis,METACHROMATIC LEUKODYSTROPHY,Metachromatic leukodystrophy adult form,METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY,Metachromatic leukodystrophy juvenile form,Metachromatic leukodystrophy late infantile form,Metaphyseal anadysplasia,Metaphyseal anadysplasia 2,METAPHYSEAL ANADYSPLASIA TYPE 1,Metaphyseal chondrodysplasia Jansen type,METAPHYSEAL CHONDRODYSPLASIA SCHMID TYPE,Metaphyseal chondrodysplasia Spahr type,Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria,METAPHYSEAL DYSPLASIA SPAHR TYPE,METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY,Metaphyseal dysplasia without hypotrichosis,Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome,METATROPIC DYSPLASIA,METHEMOGLOBINEMIA ALPHA TYPE,METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA,METHEMOGLOBINEMIA BETA TYPE,METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE,methionine adenosyltransferase deficiency,METHIONINE ADENOSYLTRANSFERASE I/III DEFICIENCY,Methylcobalamin deficiency type cblDv1,Methylcobalamin deficiency type cblE,Methylcobalamin deficiency type cblG,METHYLCOBALAMIN DEFICIENCY TYPE G,Methylenetetrahydrofolate reductase deficiency,METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY,METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA cblX TYPE,Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency,Methylmalonic acidemia with homocystinuria type cblC,Methylmalonic acidemia with homocystinuria type cblD,Methylmalonic acidemia with homocystinuria type cblF,Methylmalonic acidemia with homocystinuria type cblJ,Methylmalonic acidemia with homocystinuria type cblX,METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA cblC TYPE,METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA cblD TYPE,METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA cblF TYPE,METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA cblJ TYPE,METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA TYPE CBLD,methylmalonic aciduria and homocystinuria type cblF,METHYLMALONIC ACIDURIA cblA TYPE,METHYLMALONIC ACIDURIA cblB TYPE,METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY,METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT,METHYLMALONIC ACIDURIA TRANSIENT DUE TO TRANSCOBALAMIN RECEPTOR DEFECT,methylmalonic aciduria type cblA,Methylmalonic aciduria type cblB,methylmalonic aciduria type mut,METHYLMALONYL-CoA EPIMERASE DEFICIENCY,Metopic ridging-ptosis-facial dysmorphism syndrome,METTL23-related Intellectual Disability,MEVALONIC ACIDURIA,MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect,MFN2-related developmental disorder,MFSD8-Related Neuronal Ceroid-Lipofuscinosis,MGAT2-CDG,MIB1-related developmental disorder monoallelic,Micro syndrome,MICROANGIOPATHY AND LEUKOENCEPHALOPATHY PONTINE AUTOSOMAL DOMINANT,Microcephalic cortical malformations-short stature due to RTTN deficiency,Microcephalic dwarfism,Microcephalic osteodysplastic dysplasia Saul-Wilson type,MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM TYPE I,Microcephalic osteodysplastic primordial dwarfism type II,Microcephalic osteodysplastic primordial dwarfism types I and III,Microcephalic primordial dwarfism,Microcephalic primordial dwarfism Dauber type,Microcephalic primordial dwarfism due to ZNF335 deficiency,Microcephalic primordial dwarfism-insulin resistance syndrome,Microcephaly,MICROCEPHALY 1 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 10 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 11 PRIMARY AUTOSOMAL RECESSIVE,Microcephaly 12 primary autosomal recessive,Microcephaly 13 primary autosomal recessive,MICROCEPHALY 14 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 15 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 16 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 17 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 18 PRIMARY AUTOSOMAL DOMINANT,MICROCEPHALY 19 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 2 PRIMARY AUTOSOMAL RECESSIVE WITH OR WITHOUT CORTICAL MALFORMATIONS,MICROCEPHALY 20 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 21 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 22 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 23 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 24 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 25 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 26 PRIMARY AUTOSOMAL DOMINANT,MICROCEPHALY 27 PRIMARY AUTOSOMAL DOMINANT,MICROCEPHALY 3 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 4 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 5 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 6 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 7 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 8 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY 9 PRIMARY AUTOSOMAL RECESSIVE,MICROCEPHALY AMISH TYPE,MICROCEPHALY AND CHORIORETINOPATHY AUTOSOMAL RECESSIVE 1,Microcephaly and chorioretinopathy autosomal recessive 2,MICROCEPHALY AND CHORIORETINOPATHY AUTOSOMAL RECESSIVE 3,Microcephaly and chorioretinopathy with or without mental retardation,Microcephaly and Lissencephaly Spectrum Disorders,MICROCEPHALY CATARACTS IMPAIRED INTELLECTUAL DEVELOPMENT AND DYSTONIA WITH ABNORMAL STRIATUM,MICROCEPHALY CONGENITAL CATARACT AND PSORIASIFORM DERMATITIS,MICROCEPHALY CORTICAL MALFORMATIONS AND MENTAL RETARDATION,Microcephaly Developmental Delay and Brittle Hair and Nails,MICROCEPHALY DEVELOPMENTAL DELAY AND BRITTLE HAIR SYNDROME,MICROCEPHALY EPILEPSY AND DIABETES SYNDROME,MICROCEPHALY FACIAL DYSMORPHISM RENAL AGENESIS AND AMBIGUOUS GENITALIA SYNDROME,MICROCEPHALY GROWTH DEFICIENCY SEIZURES AND BRAIN MALFORMATIONS,Microcephaly growth failure and retinopathy,MICROCEPHALY GROWTH RESTRICTION AND INCREASED SISTER CHROMATID EXCHANGE 2,Microcephaly hearing loss and dysmorphic features,Microcephaly postnatal progressive with seizures and brain atrophy,MICROCEPHALY PRIMARY TYPE 1,microcephaly primary type 7,Microcephaly progressive seizures and cerebral and cerebellar atrophy,Microcephaly progressive with seizures and cerebral and cerebellar atrophy,MICROCEPHALY SEIZURES AND DEVELOPMENTAL DELAY,MICROCEPHALY SHORT STATURE AND IMPAIRED GLUCOSE METABOLISM 1,MICROCEPHALY SHORT STATURE AND IMPAIRED GLUCOSE METABOLISM 2,MICROCEPHALY SHORT STATURE AND LIMB ABNORMALITIES,MICROCEPHALY SHORT STATURE AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES,Microcephaly with or without chorioretinopathy lymphedema or mental retardation,Microcephaly with short stature,MICROCEPHALY-CAPILLARY MALFORMATION MIC-CAP SYNDROME,Microcephaly-capillary malformation syndrome,Microcephaly-complex motor and sensory axonal neuropathy syndrome,Microcephaly-congenital cataract-psoriasiform dermatitis syndrome,Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom,Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome,Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome,Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome,Microcephaly-lymphedema-chorioretinopathy syndrome,Microcephaly-micromelia syndrome,Microcephaly-polymicrogyria-corpus callosum agenesis syndrome,Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome,Microcephaly-short stature-limb abnormalities syndrome,Microcephaly-thin corpus callosum-intellectual disability syndrome,Microcornea myopic chorioretinal atrophy and telecanthus,MICROCORNEA ROD-CONE DYSTROPHY CATARACT AND POSTERIOR STAPHYLOMA 1,Microcornea-myopic chorioretinal atrophy-telecanthus syndrome,Microcystic stromal tumor,Microcytic anemia with liver iron overload,Microduplication Xp11.22-p11.23 syndrome,Microform holoprosencephaly,Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome,MICROHYDRANENCEPHALY,Microlissencephaly,Microphthalmia and Diaphragmatic Hernia,MICROPHTHALMIA ISOLATED 2,MICROPHTHALMIA ISOLATED 3,MICROPHTHALMIA ISOLATED 4,MICROPHTHALMIA ISOLATED 5,MICROPHTHALMIA ISOLATED 6,MICROPHTHALMIA ISOLATED 7,MICROPHTHALMIA ISOLATED 8,microphthalmia isolated type 2,MICROPHTHALMIA ISOLATED TYPE 3,MICROPHTHALMIA ISOLATED TYPE 5,MICROPHTHALMIA ISOLATED TYPE 6,MICROPHTHALMIA ISOLATED WITH CATARACT 2,MICROPHTHALMIA ISOLATED WITH CATARACT TYPE 4,MICROPHTHALMIA ISOLATED WITH COLOBOMA 10,MICROPHTHALMIA ISOLATED WITH COLOBOMA 3,MICROPHTHALMIA ISOLATED WITH COLOBOMA 5,MICROPHTHALMIA ISOLATED WITH COLOBOMA 6,Microphthalmia isolated with coloboma 7,MICROPHTHALMIA ISOLATED WITH COLOBOMA 9,microphthalmia isolated with coloboma type 5,Microphthalmia Lenz type,MICROPHTHALMIA SYNDROMIC 1,MICROPHTHALMIA SYNDROMIC 11,Microphthalmia syndromic 12,Microphthalmia syndromic 13,MICROPHTHALMIA SYNDROMIC 14,MICROPHTHALMIA SYNDROMIC 14 biallelic,MICROPHTHALMIA SYNDROMIC 2,MICROPHTHALMIA SYNDROMIC 3,MICROPHTHALMIA SYNDROMIC 5,MICROPHTHALMIA SYNDROMIC 6,MICROPHTHALMIA SYNDROMIC 9,MICROPHTHALMIA SYNDROMIC TYPE 2,MICROPHTHALMIA SYNDROMIC TYPE 3,MICROPHTHALMIA SYNDROMIC TYPE 5,MICROPHTHALMIA SYNDROMIC TYPE 7,MICROPHTHALMIA SYNDROMIC TYPE 8,MICROPHTHALMIA SYNDROMIC TYPE 9,Microphthalmia with brain and digit anomalies,MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES,MICROPHTHALMIA WITH LIMB ANOMALIES,MICROPHTHALMIA WITH LINEAR SKIN DEFECTS SYNDROME,Microphthalmia with Linear Skin Lesions,Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome,MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME,Microspherophakia,MICROSPHEROPHAKIA AND/OR MEGALOCORNEA WITH ECTOPIA LENTIS AND WITHOR WITHOUT SECONDARY GLAUCOMA,Microtia,MICROTIA HEARING IMPAIRMENT AND CLEFT PALATE MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT INCLUDED,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 1,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 2,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 3,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 4,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 5,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 6,MICROVASCULAR COMPLICATIONS OF DIABETES SUSCEPTIBILITY TO 7,MICROVILLUS INCLUSION DISEASE,Midface hypoplasia hearing impairment elliptocytosis and nephrocalcinosis,Midline interhemispheric variant of holoprosencephaly,Midline-bridging neuronal commissure disruption horizontal gaze palsy scoliosis and intellectual disability,MIGRAINE FAMILIAL HEMIPLEGIC 1,MIGRAINE FAMILIAL HEMIPLEGIC 2,MIGRAINE FAMILIAL HEMIPLEGIC 3,MIGRAINE FAMILIAL HEMIPLEGIC ATP1A2-related,MIGRAINE WITH OR WITHOUT AURA SUSCEPTIBILITY TO 1,MIGRAINE WITH OR WITHOUT AURA SUSCEPTIBILITY TO 13,Mild Canavan disease,Mild hemophilia A,Mild hemophilia B,Mild hyperphenylalaninemia,Mild phenylketonuria,Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis,Miller-Dieker syndrome,Milroy Disease,MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA,Minimal pigment oculocutaneous albinism type 1,MIRAGE - myelodysplasia infection restriction of growth adrenal hypoplasia genital phenotypes enteropathy,MIRAGE SYNDROME,MIRROR MOVEMENTS 1,MIRROR MOVEMENTS 2,MIRROR MOVEMENTS 3,MIRROR MOVEMENTS 4,Mirror-image polydactyly,MISMATCH REPAIR CANCER SYNDROME,MISMATCH REPAIR CANCER SYNDROME 1,MISMATCH REPAIR CANCER SYNDROME 2,MISMATCH REPAIR CANCER SYNDROME 3,MISMATCH REPAIR CANCER SYNDROME 4,MiT family translocation renal cell carcinoma,MITCHELL SYNDROME,Mitchell-Riley syndrome,MITF-related melanoma and renal cell carcinoma predisposition syndrome,Mitochondrial complex I deficiency,Mitochondrial complex I deficiency nuclear type 1,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 10,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 11,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 12,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 13,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 14,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 15,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 16,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 17,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 18,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 19,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 2,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 20,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 21,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 22,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 23,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 24,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 25,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 26,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 27,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 28,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 29,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 3,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 30,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 31,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 32,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 33,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 34,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 35,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 36,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 4,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 5,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 6,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 7,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 8,MITOCHONDRIAL COMPLEX I DEFICIENCY NUCLEAR TYPE 9,Mitochondrial complex II deficiency,MITOCHONDRIAL COMPLEX II DEFICIENCY NUCLEAR TYPE 1,MITOCHONDRIAL COMPLEX II DEFICIENCY NUCLEAR TYPE 2,MITOCHONDRIAL COMPLEX II DEFICIENCY NUCLEAR TYPE 3,MITOCHONDRIAL COMPLEX II DEFICIENCY NUCLEAR TYPE 4,MITOCHONDRIAL COMPLEX III DEFICIENCY,Mitochondrial Complex III Deficiency Cardiomyopathy and Alopecia Totalis,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 1,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 10,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 2,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 3,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 4,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 5,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 6,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 7,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 8,MITOCHONDRIAL COMPLEX III DEFICIENCY NUCLEAR TYPE 9,MITOCHONDRIAL COMPLEX IV DEFICIENCY,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 1,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 10,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 11,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 12,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 13,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 14,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 15,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 16,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 17,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 18,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 19,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 2,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 20,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 21,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 3,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 4,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 5,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 6,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 7,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 8,MITOCHONDRIAL COMPLEX IV DEFICIENCY NUCLEAR TYPE 9,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 1,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 2,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 3,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 4,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 5,MITOCHONDRIAL COMPLEX V ATP SYNTHASE DEFICIENCY NUCLEAR TYPE 6,Mitochondrial depletion syndrome,MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE),MITOCHONDRIAL DNA DEPLETION SYNDROME 11,MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE) AUTOSOMAL DOMINANT,MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE) AUTOSOMAL RECESSIVE,Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type),Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type),MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE),MITOCHONDRIAL DNA DEPLETION SYNDROME 16 HEPATIC TYPE,MITOCHONDRIAL DNA DEPLETION SYNDROME 17,MITOCHONDRIAL DNA DEPLETION SYNDROME 18,MITOCHONDRIAL DNA DEPLETION SYNDROME 19,MITOCHONDRIAL DNA DEPLETION SYNDROME 2 MYOPATHIC TYPE,MITOCHONDRIAL DNA DEPLETION SYNDROME 3 HEPATOCEREBRAL TYPE,Mitochondrial DNA depletion syndrome 4A,MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE),Mitochondrial DNA depletion syndrome 4B MNGIE type,Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria),MITOCHONDRIAL DNA DEPLETION SYNDROME 6,MITOCHONDRIAL DNA DEPLETION SYNDROME 6 HEPATOCEREBRAL TYPE,MITOCHONDRIAL DNA DEPLETION SYNDROME 7 HEPATOCEREBRAL TYPE,MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY),MITOCHONDRIAL DNA DEPLETION SYNDROME 9 ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA,Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria,Mitochondrial DNA depletion syndrome encephalomyopathic form with renal tubulopathy,Mitochondrial DNA depletion syndrome encephalomyopathic form with variable craniofacial anomalies,Mitochondrial DNA depletion syndrome hepatocerebral form due to DGUOK deficiency,Mitochondrial DNA depletion syndrome hepatocerebrorenal form,Mitochondrial DNA Depletion Syndrome Myopathic Form,Mitochondrial DNA-associated Leigh syndrome,Mitochondrial DNA-related cardiomyopathy and hearing loss,Mitochondrial DNA-related progressive external ophthalmoplegia,Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency,Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy,Mitochondrial membrane protein-associated neurodegeneration,Mitochondrial myopathy and sideroblastic anemia,MITOCHONDRIAL MYOPATHY ENCEPHALOPATHY LACTIC ACIDOSIS AND STROKE-LIKE EPISODES,MITOCHONDRIAL MYOPATHY EPISODIC WITH OR WITHOUT OPTIC ATROPHY ANDREVERSIBLE LEUKOENCEPHALOPATHY,Mitochondrial myopathy with lactic acidosis,Mitochondrial myopathy with reversible cytochrome C oxidase deficiency,Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome,Mitochondrial neurogastrointestinal encephalomyopathy,Mitochondrial non-syndromic sensorineural deafness,MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY,MITOCHONDRIAL PROGRESSIVE MYOPATHY WITH CONGENITAL CATARACT HEARING LOSS AND DEVELOPMENTAL DELAY (MPMCHD,MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY,MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX I DEFICIENCY,Mitochondrial Respiratory Chain Complex III Deficiency UQCRB-Related,Mitochondrial Respiratory Chain Complex III Deficiency UQCRQ Related,Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies,MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY,Mitochondrial translation defect associated with hypertrophic cardiomyopathy lactic acidosis and encephalopathy,Mitochondrial trifunctional protein deficiency,MITRAL VALVE PROLAPSE 2,MITRAL VALVE PROLAPSE 3,Mixed phenotype acute leukemia,MIYOSHI MUSCULAR DYSTROPHY 1,MIYOSHI MUSCULAR DYSTROPHY 3,MIYOSHI MYOPATHY,MME-related autosomal dominant Charcot Marie Tooth disease type 2,MMGT1-related developmental disorder,MMP21-associated heterotaxy,MN1 C-terminal truncation syndrome,Moderate multiminicore disease with hand involvement,Moderate Sensorineural Hearing Loss,Moderately severe hemophilia A,Moderately severe hemophilia B,MODY,Moebius syndrome,MOGS-CDG,Mohr-Majewski Syndrome,MOHR-TRANEBJAERG SYNDROME,Molybdenum Cofactor Deficiency,MOLYBDENUM COFACTOR DEFICIENCY COMPLEMENTATION GROUP A,MOLYBDENUM COFACTOR DEFICIENCY COMPLEMENTATION GROUP B,Molybdenum cofactor deficiency complementation group C,MONILETHRIX,Monoamine oxidase A deficiency,MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY,Monocytopenia with susceptibility to infections,Monomelic amyotrophy,MONONEUROPATHY OF THE MEDIAN NERVE MILD,Monosomy 13q14,Monosomy 22q13.3,Monosomy 5p,MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 1,MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 2,Monosomy 9q22.3,Monostotic fibrous dysplasia,Morbid obesity and spermatogenic failure,MORC2 - axonal neuropathy and neurodevelopmental disorder,MORM syndrome,Morning glory disc anomaly,Mosaic Variegated Aneuploidy and Wilms Tumour,Mosaic variegated aneuploidy syndrome,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1,Mosaic variegated aneuploidy syndrome 2,Mosaic variegated aneuploidy syndrome 3,Motile Cilia Defects and Situs Inversus,Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry,MOWAT-WILSON SYNDROME,Mowat-Wilson syndrome due to a ZEB2 point mutation,Mowat-Wilson syndrome due to monosomy 2q22,Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome,Moyamoya disease,MOYAMOYA DISEASE 2,Moyamoya disease 5,MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA,Moyamoya disease with early-onset achalasia,MPDU1-CDG,MPI-CDG,MRCS syndrome,MRX with/without nystagmus,MSH3-related attenuated familial adenomatous polyposis,MSI1-associated Microcephaly,MSL2-related developmental disorder monoallelic,MSL3 syndrome,MT-ATP6-related mitochondrial spastic paraplegia,MUC1-related autosomal dominant tubulointerstitial kidney disease,MUCKLE-WELLS SYNDROME,Mucociliary Clearance and Laterality Defects,MUCOCUTANEOUS ULCERATION CHRONIC,Mucocutaneous venous malformations,MUCOEPITHELIAL DYSPLASIA HEREDITARY,MUCOLIPIDOSIS II ALPHA/BETA,MUCOLIPIDOSIS III ALPHA/BETA,MUCOLIPIDOSIS III GAMMA,MUCOLIPIDOSIS IV,MUCOLIPIDOSIS TYPE II,Mucolipidosis Type III Alpha/Beta,Mucolipidosis type III complementation group A,MUCOLIPIDOSIS TYPE III COMPLEMENTATION GROUP C,Mucolipidosis type III gamma,Mucolipidosis type IV,MUCOPOLYSACCHARIDOSIS TYPE 1S,MUCOPOLYSACCHARIDOSIS TYPE 2,Mucopolysaccharidosis type 2 attenuated form,Mucopolysaccharidosis type 2 severe form,MUCOPOLYSACCHARIDOSIS TYPE 3A,MUCOPOLYSACCHARIDOSIS TYPE 3B,MUCOPOLYSACCHARIDOSIS TYPE 3C,MUCOPOLYSACCHARIDOSIS TYPE 3D,Mucopolysaccharidosis type 4A,Mucopolysaccharidosis type 4B,MUCOPOLYSACCHARIDOSIS TYPE 6,Mucopolysaccharidosis type 6 rapidly progressing,Mucopolysaccharidosis type 6 slowly progressing,Mucopolysaccharidosis type 7,MUCOPOLYSACCHARIDOSIS TYPE 9,MUCOPOLYSACCHARIDOSIS TYPE II,MUCOPOLYSACCHARIDOSIS TYPE IIIA,MUCOPOLYSACCHARIDOSIS TYPE IIIB,MUCOPOLYSACCHARIDOSIS TYPE IIIC,MUCOPOLYSACCHARIDOSIS TYPE IIID,MUCOPOLYSACCHARIDOSIS TYPE IVA,MUCOPOLYSACCHARIDOSIS TYPE IVB,MUCOPOLYSACCHARIDOSIS TYPE IX,MUCOPOLYSACCHARIDOSIS TYPE VI,MUCOPOLYSACCHARIDOSIS TYPE VII,Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders,MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME,MUENKE SYNDROME,Muir-Torre syndrome,MULIBREY NANISM,MULLEGAMA-KLEIN-MARTINEZ SYNDROME,Mullerian aplasia and hyperandrogenism,Multicentric carpo-tarsal osteolysis with or without nephropathy,MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME,MULTICENTRIC OSTEOLYSIS NODULOSIS AND ARTHROPATHY,Multicentric osteolysis-nodulosis-arthropathy spectrum,Multifocal pattern dystrophy simulating fundus flavimaculatus,MULTINUCLEATED NEURONS ANHYDRAMNIOS RENAL DYSPLASIA CEREBELLAR HYPOPLASIA AND HYDRANENCEPHALY,Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome,MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY,Multiple acyl-CoA dehydrogenase deficiency mild type,Multiple acyl-CoA dehydrogenase deficiency severe neonatal type,Multiple benign circumferential skin creases on limbs,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4,Multiple congenital anomalies-hypotonia-seizures syndrome type 2,MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME X-LINKED,Multiple endocrine neoplasia IIB,Multiple endocrine neoplasia type 1,Multiple endocrine neoplasia type 2A,Multiple endocrine neoplasia type 2B,Multiple endocrine neoplasia type 4,MULTIPLE ENDOCRINE NEOPLASIA TYPE I,MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA,MULTIPLE ENDOCRINE NEOPLASIA TYPE IIB,MULTIPLE ENDOCRINE NEOPLASIA TYPE IV,Multiple epiphyseal dysplasia Al-Gazali type,Multiple epiphyseal dysplasia Beighton type,Multiple epiphyseal dysplasia due to collagen 9 anomaly,Multiple epiphyseal dysplasia type 1,MULTIPLE EPIPHYSEAL DYSPLASIA TYPE 2,MULTIPLE EPIPHYSEAL DYSPLASIA TYPE 3,Multiple epiphyseal dysplasia type 4,Multiple epiphyseal dysplasia type 5,MULTIPLE EPIPHYSEAL DYSPLASIA TYPE 6,MULTIPLE FIBROADENOMAS OF THE BREAST,Multiple intestinal atresia,MULTIPLE JOINT DISLOCATIONS SHORT STATURE AND CRANIOFACIAL DYSMORPHISMWITH OR WITHOUT CONGENITAL HEART DEFECTS,Multiple malformations of neural tube ear genitourinary and gastrointestinal systems,Multiple mitochondrial dysfunctions syndrome 1,Multiple mitochondrial dysfunctions syndrome 2,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6,Multiple mitochondrial dysfunctions syndrome type 1,Multiple mitochondrial dysfunctions syndrome type 2,Multiple mitochondrial dysfunctions syndrome type 3,Multiple mitochondrial dysfunctions syndrome type 4,Multiple mitochondrial dysfunctions syndrome type 5,Multiple mitochondrial dysfunctions syndrome type 6,Multiple myeloma,Multiple osteochondromas,Multiple paragangliomas associated with polycythemia,MULTIPLE PTERYGIUM SYNDROME ESCOBAR VARIANT,MULTIPLE PTERYGIUM SYNDROME LETHAL TYPE,MULTIPLE SCLEROSIS SUSCEPTIBILITY TO,MULTIPLE SCLEROSIS SUSCEPTIBILITY TO 5,Multiple self-healing squamous epithelioma,MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA SUSCEPTIBILITY TO,MULTIPLE SULFATASE DEFICIENCY,Multiple symmetric lipomatosis,Multiple synostoses syndrome,MULTIPLE SYNOSTOSES SYNDROME 1,MULTIPLE SYNOSTOSES SYNDROME 2,MULTIPLE SYNOSTOSES SYNDROME 3,MULTIPLE SYNOSTOSES SYNDROME 4,multiple synostoses syndrome type 3,MULTIPLE SYSTEM ATROPHY 1 SUSCEPTIBILITY TO,Multiple system atrophy cerebellar type,Multiple system atrophy parkinsonian type,MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME,MUNGAN SYNDROME,Muscle filaminopathy,MUSCLE HYPERTROPHY,Muscle Weakness and Isolated Complex I Deficiency,Muscle-eye-brain disease,Muscle-eye-brain disease with bilateral multicystic leucodystrophy,MUSCULAR DYSTROPHY AUTOSOMAL RECESSIVE WITH CARDIOMYOPATHY AND TRIANGULAR TONGUE,MUSCULAR DYSTROPHY BECKER TYPE,Muscular dystrophy congenital davignon-chauveau type,MUSCULAR DYSTROPHY CONGENITAL DUE TO INTEGRIN ALPHA-7 DEFICIENCY,MUSCULAR DYSTROPHY CONGENITAL LMNA-RELATED,Muscular dystrophy congenital megaconial type,MUSCULAR DYSTROPHY CONGENITAL MEROSIN-DEFICIENT 1A,MUSCULAR DYSTROPHY CONGENITAL WITH CATARACTS AND INTELLECTUAL DISABILITY,MUSCULAR DYSTROPHY DUCHENNE TYPE,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL DOMINANT 1,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL DOMINANT 2,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL DOMINANT 3,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL DOMINANT 4,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 1,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 10,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 12,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 17,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 18,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 2,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 21,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 23,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 25,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 26,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 3,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 4,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 5,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 6,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 7,MUSCULAR DYSTROPHY LIMB-GIRDLE AUTOSOMAL RECESSIVE 8,Muscular dystrophy limb-girdle type 2Q,Muscular dystrophy limb-girdle type 2S,Muscular dystrophy Selcen type,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 1,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 11,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 12,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 13,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 14,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 2,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 3,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 4,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 5,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 6,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 7,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A 9,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A1,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A2,muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies type A3 (MDDGA3,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A5,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYEANOMALIES TYPE A 10,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYEANOMALIES TYPE A 8,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 14,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 15,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 2,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 3,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 6,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH IMPAIRED INTELLECTUAL IMPAIRMENT TYPE B 1,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH MENTAL RETARDATION TYPE B6,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 5,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT TYPE B 4,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 1,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 12,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 14,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 15,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 2,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 3,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 4,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 5,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 7,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 8,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C 9,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C3,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C4,MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C7,Musculocontractural Ehlers-Danlos syndrome,Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal Recessive Cutis Laxa,Mutilating hereditary sensory neuropathy with spastic paraplegia,Mutilating palmoplantar keratoderma with periorificial keratotic plaques,MUTYH-related attenuated familial adenomatous polyposis,MYASTHENIC SYNDROME CONGENITAL 10,MYASTHENIC SYNDROME CONGENITAL 11 ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY,MYASTHENIC SYNDROME CONGENITAL 12,MYASTHENIC SYNDROME CONGENITAL 13,MYASTHENIC SYNDROME CONGENITAL 14,Myasthenic syndrome congenital 15,MYASTHENIC SYNDROME CONGENITAL 16,MYASTHENIC SYNDROME CONGENITAL 17,MYASTHENIC SYNDROME CONGENITAL 18,Myasthenic syndrome congenital 19,MYASTHENIC SYNDROME CONGENITAL 1A SLOW-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 1B FAST-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 20 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 21 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 22,MYASTHENIC SYNDROME CONGENITAL 23 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 24 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 25 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 2A SLOW-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 2C ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY,MYASTHENIC SYNDROME CONGENITAL 3A SLOW-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 3B FAST-CHANNEL,Myasthenic syndrome congenital 3c associated with acetylcholine receptor deficiency,MYASTHENIC SYNDROME CONGENITAL 4A SLOW-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 4B FAST-CHANNEL,MYASTHENIC SYNDROME CONGENITAL 4C ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY,MYASTHENIC SYNDROME CONGENITAL 5,MYASTHENIC SYNDROME CONGENITAL 6 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 7 PRESYNAPTIC,MYASTHENIC SYNDROME CONGENITAL 8,MYASTHENIC SYNDROME CONGENITAL 9 ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY,MYASTHENIC SYNDROME CONGENITAL WITH TUBULAR AGGREGATES 2,MYBPC1-related arthrogryposis and myopathy,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome,MYCOBACTERIUM TUBERCULOSIS SUSCEPTIBILITY TO MYCOBACTERIUM TUBERCULOSIS PROTECTION AGAINST INCLUDED,MYELODYSPLASTIC SYNDROME,Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality,MYELOFIBROSIS MYELOFIBROSIS WITH MYELOID METAPLASIA INCLUDED,Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement,Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement,Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement,MYELOMA MULTIPLE AMYLOIDOSIS SYSTEMIC INCLUDED,MYELOPEROXIDASE DEFICIENCY,MYELOPROLIFERATIVE DISORDER CHRONIC WITH EOSINOPHILIA,MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS FAMILIAL (MULTIPLE TYPES) SUSCEPTIBILITY TO,MYH10-related Multiple congenital anomalies,MYH7-related late-onset scapuloperoneal muscular dystrophy,MYH9-related disease,Myhre syndrome,MYLPF arthrogryposis biallelic,MYLPF arthrogryposis monoallelic,MYO5B-related progressive familial intrahepatic cholestasis,MYOCARDIAL INFARCTION SUSCEPTIBILITY TO MYOCARDIAL INFARCTION SUSCEPTIBILITY TO 1 INCLUDED,MYOCLONIC EPILEPSY FAMILIAL INFANTILE,Myoclonic epilepsy infantile familial,MYOCLONIC EPILEPSY OF LAFORA,MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG,Myoclonic-astatic epilepsy,MYOCLONIC-ATONIC EPILEPSY,MYOCLONUS FAMILIAL 1,MYOCLONUS FAMILIAL 2,MYOCLONUS INTRACTABLE NEONATAL,MYOCLONUS-DYSTONIA SYNDROME,MYOFIBRILLAR MYOPATHY 10,MYOFIBRILLAR MYOPATHY 11,MYOFIBROMATOSIS INFANTILE 1,MYOFIBROMATOSIS INFANTILE 2,Myoglobinuria acute recurrent autosomal recessive,Myopathic Ehlers-Danlos syndrome,Myopathic intestinal pseudoobstruction,Myopathy and diabetes mellitus,Myopathy areflexia respiratory distress and dysphagia early-onset,MYOPATHY AUTOSOMAL RECESSIVE WITH RIGID SPINE AND DISTAL JOINT CONTRACTURES,MYOPATHY CENTRONUCLEAR 1,MYOPATHY CENTRONUCLEAR 2,MYOPATHY CENTRONUCLEAR 4,Myopathy centronuclear 5,MYOPATHY CENTRONUCLEAR 6 WITH FIBER-TYPE DISPROPORTION,MYOPATHY CENTRONUCLEAR X-LINKED,MYOPATHY CONGENITAL BAILEY-BLOCH,MYOPATHY CONGENITAL COMPTON-NORTH,MYOPATHY CONGENITAL PROGRESSIVE WITH SCOLIOSIS,MYOPATHY CONGENITAL PROXIMAL WITH MINICORE LESIONS,MYOPATHY CONGENITAL WITH DIAPHRAGMATIC DEFECTS RESPIRATORY INSUFFICIENCY AND DYSMORPHIC FACIES,MYOPATHY CONGENITAL WITH FAST-TWITCH (TYPE II) FIBER ATROPHY,MYOPATHY CONGENITAL WITH FIBER-TYPE DISPROPORTION,MYOPATHY CONGENITAL WITH RESPIRATORY INSUFFICIENCY AND BONE FRACTURES,MYOPATHY CONGENITAL WITH STRUCTURED CORES AND Z-LINE ABNORMALITIES,MYOPATHY CONGENITAL WITH TREMOR,MYOPATHY DISTAL 1,MYOPATHY DISTAL 4,MYOPATHY DISTAL 5,MYOPATHY DISTAL 6 ADULT-ONSET AUTOSOMAL DOMINANT,MYOPATHY DISTAL TATEYAMA TYPE,MYOPATHY DISTAL WITH ANTERIOR TIBIAL ONSET,MYOPATHY DISTAL WITH RIMMED VACUOLES,MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY,Myopathy early-onset areflexia respiratory distress and dysphagia,MYOPATHY EPILEPSY AND PROGRESSIVE CEREBRAL ATROPHY,Myopathy isolated mitochondrial autosomal dominant,MYOPATHY LACTIC ACIDOSIS AND SIDEROBLASTIC ANEMIA 1,MYOPATHY LACTIC ACIDOSIS AND SIDEROBLASTIC ANEMIA 2,MYOPATHY MITOCHONDRIAL AND ATAXIA,MYOPATHY MITOCHONDRIAL PROGRESSIVE WITH CONGENITAL CATARACT AND DEVELOPMENTAL DELAY,MYOPATHY MYOFIBRILLAR 1,Myopathy myofibrillar 2,MYOPATHY MYOFIBRILLAR 3,MYOPATHY MYOFIBRILLAR 4,MYOPATHY MYOFIBRILLAR 5,Myopathy myofibrillar 6,MYOPATHY MYOFIBRILLAR 7,MYOPATHY MYOFIBRILLAR 8,MYOPATHY MYOFIBRILLAR 9 WITH EARLY RESPIRATORY FAILURE,Myopathy myofibrillar fatal infantile hypertonic alpha-B crystallin-related,MYOPATHY MYOFIBRILLAR TYPE 4,MYOPATHY MYOSIN STORAGE AUTOSOMAL DOMINANT,MYOPATHY MYOSIN STORAGE AUTOSOMAL RECESSIVE,MYOPATHY PROXIMAL WITH OPHTHALMOPLEGIA,MYOPATHY SCAPULOHUMEROPERONEAL,MYOPATHY SPHEROID BODY,MYOPATHY TUBULAR AGGREGATE 1,Myopathy tubular aggregate 2,Myopathy vacuolar with casq1 aggregates,Myopathy with extrapyramidal signs,MYOPATHY WITH LACTIC ACIDOSIS HEREDITARY,MYOPATHY X-LINKED WITH EXCESSIVE AUTOPHAGY,MYOPATHY X-LINKED WITH POSTURAL MUSCLE ATROPHY,MYOPIA 21 AUTOSOMAL DOMINANT,MYOPIA 22 AUTOSOMAL DOMINANT,Myopia 23 autosomal recessive,MYOPIA 24 AUTOSOMAL DOMINANT,MYOPIA 25 AUTOSOMAL DOMINANT,MYOPIA 26 X-LINKED FEMALE-LIMITED,MYOPIA 27,Myopia 6,MYOPIA HIGH WITH CATARACT AND VITREORETINAL DEGENERATION,Myosclerosis,MYOSCLEROSIS AUTOSOMAL RECESSIVE,Myostatin-related muscle hypertrophy,MYOTONIA CONGENITA AUTOSOMAL DOMINANT,MYOTONIA CONGENITA AUTOSOMAL RECESSIVE,MYOTONIA FLUCTUANS,MYOTONIA PERMANENS,MYOTONIA POTASSIUM-AGGRAVATED,MYOTONIC DYSTROPHY 1,MYOTONIC DYSTROPHY 2,MYOTUBULAR MYOPATHY X-LINKED,MYSM1-related congenital bone marrow failure,MYT1L syndrome,Myxofibrosarcoma,Myxoid/round cell liposarcoma,MYXOMA INTRACARDIAC,N-ACETYLASPARTATE DEFICIENCY,N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY,NABAIS SA-DE VRIES SYNDROME TYPE 1,NABAIS SA-DE VRIES SYNDROME TYPE 2,NADPH DEHYDROGENASE QUINONE 1,NADPHX dehydratase deficiency,NADPHX epimerase deficiency,NADSYN1-related Congenital NAD Deficiency Disorder,Naegeli-Franceschetti-Jadassohn syndrome,Nager syndrome,Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome,NAIL DISORDER NON-SYNDROMIC CONGENITAL TYPE 10,NAIL DISORDER NONSYNDROMIC CONGENITAL 1,NAIL DISORDER NONSYNDROMIC CONGENITAL 3,NAIL DISORDER NONSYNDROMIC CONGENITAL 4,NAIL DISORDER NONSYNDROMIC CONGENITAL 8,NAIL-PATELLA SYNDROME,Nail-patella-like renal disease,Nakajo syndrome,NANCE-HORAN SYNDROME,Nanophthalmos,NANOPHTHALMOS 2,Nanophthalmos 4,NAPB-related Neurodevelopmental Disorder,NARCOLEPSY 1,NARCOLEPSY 7,Narcolepsy type 1,Narcolepsy type 2,NARP syndrome,NARS1 Neurodevelopmental Disorder biallelic,NARS1 Neurodevelopmental Disorder monoallelic,NASOPHARYNGEAL CARCINOMA,NASOPHARYNGEAL CARCINOMA SUSCEPTIBILITY TO 3,Nasu-Hakola disease,NATIVE AMERICAN MYOPATHY,Navajo neurohepatopathy,NAXOS DISEASE,NBEA Neurodevelopment disorder with seizures,NCDN-associated neurodevelopmental disorder with seizures biallelic,NCDN-associated neurodevelopmental disorder with seizures monoallelic,NCKAP1-related Neurodevelopmental Disorder,NCOR1-related developmental disorder,NDE1-related microhydranencephaly,NDNF-related Congenital Hypogonadotrophic Hypogonadism,NDUFA8-related developmental disorder,NDUFAF8-related Leigh Syndrome,NDUFB7-associated lactic acidosis and hypertrophic cardiomyopathy,NEK9-related lethal skeletal dysplasia,NEMALINE MYOPATHY 1,Nemaline myopathy 10,NEMALINE MYOPATHY 11 AUTOSOMAL RECESSIVE,Nemaline myopathy 2,NEMALINE MYOPATHY 3,NEMALINE MYOPATHY 4,NEMALINE MYOPATHY 5,Nemaline myopathy 6,NEMALINE MYOPATHY 7,Nemaline myopathy 8,Nemaline myopathy 8 autosomal recessive,NEMALINE MYOPATHY 9,Neonatal acute respiratory distress due to SP-B deficiency,NEONATAL ADRENOLEUKODYSTROPHY,Neonatal alloimmune neutropenia,Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome,Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome,Neonatal epilepsy spectrum,Neonatal epileptic encephalopathy due to glutaminase deficiency,Neonatal glycine encephalopathy,Neonatal ichthyosis-sclerosing cholangitis syndrome,Neonatal inflammatory skin and bowel disease,Neonatal intrahepatic cholestasis due to citrin deficiency,Neonatal Marfan syndrome,Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect,Neonatal severe primary hyperparathyroidism,Neonatal-onset epilepsy defective mitochondrial energy metabolism and glycine elevation,Nephroblastoma,Nephrogenic diabetes insipidus,NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS,NEPHROLITHIASIS CALCIUM OXALATE,NEPHROLITHIASIS URIC ACID SUSCEPTIBILITY TO,NEPHROLITHIASIS X-LINKED RECESSIVE WITH RENAL FAILURE,NEPHROLITHIASIS/OSTEOPOROSIS HYPOPHOSPHATEMIC 1,NEPHROLITHIASIS/OSTEOPOROSIS HYPOPHOSPHATEMIC 2,NEPHRONOPHTHISIS 1,NEPHRONOPHTHISIS 11,NEPHRONOPHTHISIS 12,NEPHRONOPHTHISIS 13,Nephronophthisis 14,NEPHRONOPHTHISIS 15,Nephronophthisis 16,NEPHRONOPHTHISIS 18,Nephronophthisis 19,NEPHRONOPHTHISIS 2,NEPHRONOPHTHISIS 20,NEPHRONOPHTHISIS 3,NEPHRONOPHTHISIS 4,Nephronophthisis 7,NEPHRONOPHTHISIS 9,Nephronophthisis Related Ciliopathy,NEPHRONOPHTHISIS TYPE 1,NEPHRONOPHTHISIS TYPE 11,NEPHRONOPHTHISIS TYPE 3,NEPHRONOPHTHISIS TYPE 4,NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1,NEPHRONOPHTHISIS-LIKE NEPHROPATHY TYPE 1,nephropathy with pretibial epidermolysis bullosa and deafness,NEPHROTIC SYNDROME TYPE 1,Nephrotic syndrome type 10,Nephrotic syndrome type 11,NEPHROTIC SYNDROME TYPE 12,NEPHROTIC SYNDROME TYPE 13,NEPHROTIC SYNDROME TYPE 14,NEPHROTIC SYNDROME TYPE 15,NEPHROTIC SYNDROME TYPE 16,NEPHROTIC SYNDROME TYPE 17,NEPHROTIC SYNDROME TYPE 18,NEPHROTIC SYNDROME TYPE 19,NEPHROTIC SYNDROME TYPE 2,NEPHROTIC SYNDROME TYPE 20,NEPHROTIC SYNDROME TYPE 21,NEPHROTIC SYNDROME TYPE 22,NEPHROTIC SYNDROME TYPE 23,NEPHROTIC SYNDROME TYPE 3,NEPHROTIC SYNDROME TYPE 4,Nephrotic syndrome type 5 with or without ocular abnormalities,NEPHROTIC SYNDROME TYPE 6,NEPHROTIC SYNDROME TYPE 7,NEPHROTIC SYNDROME TYPE 8,Nephrotic syndrome type 9,Nephrotic syndrome with primary microcephaly,Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome,NESCAV SYNDROME,Nestor-Guillermo progeria syndrome,NETHERTON SYNDROME,NEU-LAXOVA,Neu-Laxova syndrome,NEU-LAXOVA SYNDROME 1,Neu-laxova syndrome 2,Neural tube defect,NEURAL TUBE DEFECTS,Neural tube defects folate-sensitive,Neural tube defects susceptibility to,Neuralgic amyotrophy,NEURAMINIDASE DEFICIENCY,Neuro immuno skeletal Dysplasia Syndrome,Neuroblastoma,NEUROBLASTOMA SUSCEPTIBILITY TO 1,NEUROBLASTOMA SUSCEPTIBILITY TO 2,NEUROBLASTOMA SUSCEPTIBILITY TO 3,NEURODEGENERATION CHILDHOOD-ONSET STRESS-INDUCED WITH VARIABLE ATAXIA AND SEIZURES,NEURODEGENERATION CHILDHOOD-ONSET WITH ATAXIA TREMOR OPTIC ATROPHY AND COGNITIVE DECLINE,NEURODEGENERATION CHILDHOOD-ONSET WITH BRAIN ATROPHY,NEURODEGENERATION CHILDHOOD-ONSET WITH CEREBELLAR ATROPHY,NEURODEGENERATION CHILDHOOD-ONSET WITH HYPOTONIA RESPIRATORY INSUFFICIENCY AND BRAIN IMAGING ABNORMALITIES,Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency,NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY,NEURODEGENERATION EARLY-ONSET WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA,Neurodegeneration in Early Childhood,NEURODEGENERATION INFANTILE-ONSET BIOTIN-RESPONSIVE,NEURODEGENERATION WITH ATAXIA DYSTONIA AND GAZE PALSY CHILDHOOD-ONSET,Neurodegeneration with brain iron accumulation,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4,Neurodegeneration with brain iron accumulation 5,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8,Neurodegeneration with Developmental Delay Ataxia and Axonal Neuropathy,Neurodegenerative disorder exacerbated by febrile illnesses,Neurodegenerative syndrome due to cerebral folate transport deficiency,Neurodevelopment disorder,Neurodevelopmental Cardiac and Renal Syndrome,Neurodevelopmental Delay Congenital Heart Defects and Distinct Facial Dysmorphism,Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome,Neurodevelopmental Disease Associated with Mild Dysmorphism,Neurodevelopmental disorder,NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES,NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY,Neurodevelopmental Disorder in Females,NEURODEVELOPMENTAL DISORDER MITOCHONDRIAL WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS WITH OR WITHOUT SEIZURES,Neurodevelopmental Disorder of Hypusination,NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES,NEURODEVELOPMENTAL DISORDER WITH ATAXIA HYPOTONIA AND MICROCEPHALY,NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT ABSENT SPEECH AND DECREASED CORTICAL WHITE MATTER,NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES ABSENT SPEECH AND HYPOTONIA,NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES SEIZURES AND SCOLIOSIS,NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY SPASTICITY AND BRAIN ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH CATARACTS POOR GROWTH AND DYSMORPHIC FACIES,NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY,NEURODEVELOPMENTAL DISORDER WITH COARSE FACIES AND MILD DISTAL SKELETAL ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES IMPAIRED SPEECH AND HYPOTONIA,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES SLEEP DISTURBANCE AND BRAIN ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM,Neurodevelopmental disorder with epilepsy cataracts feeding difficulties and delayed brain myelination,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY SPASTICITY AND BRAIN ATROPHY,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY WITH OR WITHOUT SEIZURES,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND IMPAIRED EXPRESSIVE LANGUAGE AND WITH OR WITHOUT SEIZURES,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA MICROCEPHALY AND SEIZURES,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA NEONATAL RESPIRATORY INSUFFICIENCY AND THERMODYSREGULATION,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA NEUROPATHY AND DEAFNESS,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA SEIZURES AND ABSENT LANGUAGE,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT HYPOTONIA AND ATAXIA,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS,NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY ARTHROGRYPOSIS AND STRUCTURAL BRAIN ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY ATAXIA AND SEIZURES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY CATARACTS AND RENAL ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY CORTICAL MALFORMATIONS AND SPASTICITY,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY EPILEPSY AND BRAIN ATROPHY,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY EPILEPSY AND HYPOMYELINATION,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY HYPOTONIA AND VARIABLE BRAIN ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY IMPAIRED LANGUAGE AND GAIT ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY IMPAIRED LANGUAGE EPILEPSY AND GAIT ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SEIZURES AND BRAIN ATROPHY,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SEIZURES AND CORTICAL ATROPHY,Neurodevelopmental disorder with midbrain and hindbrain malformations,NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES ABNORMAL GAIT AND AUTISTIC FEATURES,NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN EYE OR HEART,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND/OR STRUCTURAL BRAIN ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY,Neurodevelopmental disorder with or without hyperkinetic movements and seizures autosomal dominant,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES AUTOSOMAL RECESSIVE,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY SPASTICITY AND BRAIN ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY SPASTICITY AND BRAIN IMAGING ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE SPASTICITY AND BRAIN WHITE MATTER ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH REGRESSION ABNORMAL MOVEMENTS LOSS OF SPEECH AND SEIZURES,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT,NEURODEVELOPMENTAL DISORDER WITH SEIZURES HYPOTONIA AND BRAIN IMAGING ABNORMALITIES,NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE,NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS,NEURODEVELOPMENTAL DISORDER WITH SPASTIC PARAPLEGIA AND MICROCEPHALY,NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES,NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA OPTIC ATROPHY SEIZURES AND STRUCTURAL BRAIN ANOMALIES,NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH,NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES,NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES,NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES,Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion,Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation,NEURODEVELOPMENTAL JAW EYE AND DIGITAL SYNDROME,Neuroectodermal melanolysosomal disease,Neuroendocrine tumor of stomach,NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS,Neuroferritinopathy,NEUROFIBROMATOSIS FAMILIAL SPINAL,NEUROFIBROMATOSIS TYPE 1,Neurofibromatosis type 1 due to NF1mutation or intragenic deletion,Neurofibromatosis type 2,NEUROFIBROMATOSIS TYPE I,NEUROFIBROMATOSIS TYPE II,Neurofibromatosis-Noonan syndrome,Neurogenic arthrogryposis multiplex congenita,Neurogenic scapuloperoneal syndrome Kaeser type,NEUROLOGIC ENDOCRINE AND PANCREATIC DISEASE MULTISYSTEM INFANTILE-ONSET,Neurological conditions associated with aminoacylase 1 deficiency,Neurological Phenotypes,Neurological Syndrome Fetal Akinesia /Epileptic Encephalopathy,Neurometabolic disorder due to FARS2 deficiency,NEUROMUSCULAR OCULOAUDITORY SYNDROME,Neuromyotonia and axonal neuropathy autosomal recessive,Neuronal Ceroid Lipofuscinosis,NEURONAL CEROID LIPOFUSCINOSIS TYPE 1,NEURONAL CEROID LIPOFUSCINOSIS TYPE 10,NEURONAL CEROID LIPOFUSCINOSIS TYPE 2,NEURONAL CEROID LIPOFUSCINOSIS TYPE 3,NEURONAL CEROID LIPOFUSCINOSIS TYPE 5,NEURONAL CEROID LIPOFUSCINOSIS TYPE 8,Neuronal intestinal pseudoobstruction,Neuronal intranuclear inclusion disease,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE IIA,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE IIB,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE IIC,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE IID,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE IX,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VA,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VB,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VC,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VIIA,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VIIB,NEURONOPATHY DISTAL HEREDITARY MOTOR TYPE VIII,NEUROOCULOCARDIOGENITOURINARY SYNDROME,NEUROPATHY ATAXIA AND RETINITIS PIGMENTOSA,Neuropathy congenital hypomyelinating 1,NEUROPATHY CONGENITAL HYPOMYELINATING 1 AUTOSOMAL RECESSIVE,NEUROPATHY CONGENITAL HYPOMYELINATING 2,NEUROPATHY CONGENITAL HYPOMYELINATING 3,Neuropathy hereditary motor and sensory Okinawa type,NEUROPATHY HEREDITARY MOTOR AND SENSORY RUSSE TYPE,NEUROPATHY HEREDITARY MOTOR AND SENSORY TYPE VIA WITH OPTIC ATROPHY,NEUROPATHY HEREDITARY MOTOR AND SENSORY TYPE VIB WITH OPTIC ATROPHY,NEUROPATHY HEREDITARY MOTOR AND SENSORY TYPE VIC WITH OPTIC ATROPHY,NEUROPATHY HEREDITARY MOTOR WITH MYOPATHIC FEATURES,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE IA,Neuropathy hereditary sensory and autonomic type IC,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE IIA,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE IIB,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE III,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE V,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE VI,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE VII,NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE VIII,Neuropathy hereditary sensory type ID,NEUROPATHY HEREDITARY SENSORY TYPE IE,NEUROPATHY HEREDITARY SENSORY TYPE IF,Neuropathy hereditary sensory type IIC,NEUROPATHY HEREDITARY SENSORY WITH SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE,NEUROPATHY HEREDITARY WITH LIABILITY TO PRESSURE PALSIES,NEUROPATHY HEREDITARY WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION,Neuropathy with hearing impairment,Neutral lipid storage disease with ichthyosis,NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY,Neutral lipid storage myopathy,NEUTROPENIA NONIMMUNE CHRONIC IDIOPATHIC OF ADULTS,NEUTROPENIA SEVERE CONGENITAL 1 AUTOSOMAL DOMINANT,NEUTROPENIA SEVERE CONGENITAL 2 AUTOSOMAL DOMINANT,NEUTROPENIA SEVERE CONGENITAL 3 AUTOSOMAL RECESSIVE,NEUTROPENIA SEVERE CONGENITAL 4 AUTOSOMAL RECESSIVE,NEUTROPENIA SEVERE CONGENITAL 5 AUTOSOMAL RECESSIVE,NEUTROPENIA SEVERE CONGENITAL 6 AUTOSOMAL RECESSIVE,Neutropenia severe congenital 7 autosomal recessive,NEUTROPENIA SEVERE CONGENITAL 8 AUTOSOMAL DOMINANT,NEUTROPENIA SEVERE CONGENITAL X-LINKED,NEUTROPHIL IMMUNODEFICIENCY SYNDROME,NEUTROPHILIC DERMATOSIS ACUTE FEBRILE,NEVUS COMEDONICUS,Nevus comedonicus syndrome,NEVUS EPIDERMAL,NEWFOUNDLAND ROD-CONE DYSTROPHY,NEXMIF-related Intellectual disability and epilepsy XLD,NEXMIF-related Intellectual disability and epilepsy XLR,NFE2L2-related leukoencephalopathy immune deficiency and hypohomocysteinaemia,NICOLAIDES-BARAITSER SYNDROME,Niemann-Pick disease type A,Niemann-Pick disease type B,Niemann-Pick disease type C adult neurologic onset,Niemann-Pick disease type C juvenile neurologic onset,Niemann-Pick disease type C late infantile neurologic onset,Niemann-Pick disease type C severe early infantile neurologic onset,Niemann-Pick disease type C severe perinatal form,NIEMANN-PICK DISEASE TYPE C1,NIEMANN-PICK DISEASE TYPE C2,NIGHT BLINDNESS CONGENITAL STATIONARY AUTOSOMAL DOMINANT 1,NIGHT BLINDNESS CONGENITAL STATIONARY AUTOSOMAL DOMINANT 2,NIGHT BLINDNESS CONGENITAL STATIONARY AUTOSOMAL DOMINANT 3,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1A,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1B,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1C,Night blindness congenital stationary type 1D,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1E,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1F,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1G,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 1H,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE 2A,NIGHT BLINDNESS CONGENITAL STATIONARY TYPE1I,NIJMEGEN BREAKAGE SYNDROME,NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER,NIK deficiency,NITRIC OXIDE SYNTHASE 3,NIVELON-NIVELON-MABILLE SYNDROME,NIZON-ISIDOR SYNDROME,NKX6-2-related autosomal recessive hypomyelinating leukodystrophy,NLRC4-related familial cold autoinflammatory syndrome,NLRP12-associated hereditary periodic fever syndrome,NOCTURNAL FRONTAL LOBE EPILEPSY TYPE 1,Nodular fasciitis,Nodular urticaria pigmentosa,NOG-related-symphalangism spectrum disorder,NON RARE IN EUROPE: Age-related macular degeneration,NON RARE IN EUROPE: Aldosterone-producing adenoma,NON RARE IN EUROPE: Alzheimer disease,NON RARE IN EUROPE: Ankylosing spondylitis,NON RARE IN EUROPE: Asperger syndrome,NON RARE IN EUROPE: Autism,NON RARE IN EUROPE: Autosomal dominant ichthyosis vulgaris,NON RARE IN EUROPE: Barrett esophagus,NON RARE IN EUROPE: Benign familial hematuria,NON RARE IN EUROPE: Berger disease,NON RARE IN EUROPE: Brachydactyly type D,NON RARE IN EUROPE: Celiac disease,NON RARE IN EUROPE: Congenital isolated thyroxine-binding globulin deficiency,NON RARE IN EUROPE: Crohn disease,NON RARE IN EUROPE: Dementia with Lewy body,NON RARE IN EUROPE: Diabetes mellitus type 1,NON RARE IN EUROPE: Essential hypertension,NON RARE IN EUROPE: Exfoliation syndrome,NON RARE IN EUROPE: Familial dysalbuminemic hyperthyroxinemia,NON RARE IN EUROPE: Familial hypobetalipoproteinemia,NON RARE IN EUROPE: Familial isolated hypertrophic cardiomyopathy,NON RARE IN EUROPE: FG syndrome phenotypic spectrum,NON RARE IN EUROPE: Gilbert syndrome,NON RARE IN EUROPE: Glucose-6-phosphate-dehydrogenase deficiency,NON RARE IN EUROPE: Hemochromatosis type 1,NON RARE IN EUROPE: Hereditary essential tremor,NON RARE IN EUROPE: Heterozygous familial hypercholesterolemia,NON RARE IN EUROPE: Hidradenitis suppurativa,NON RARE IN EUROPE: Hyperlipoproteinemia type 4,NON RARE IN EUROPE: Hypodontia,NON RARE IN EUROPE: Idiopathic infantile nystagmus,NON RARE IN EUROPE: Immunoglobulin A deficiency,NON RARE IN EUROPE: Infantile capillary hemangioma,NON RARE IN EUROPE: Isolated keratoconus,NON RARE IN EUROPE: Lactase non-persistence in adulthood,NON RARE IN EUROPE: Melanoma,NON RARE IN EUROPE: Metabolic syndrome,NON RARE IN EUROPE: Multiple sclerosis,NON RARE IN EUROPE: Non rare obesity,NON RARE IN EUROPE: Non rare thrombophilia,NON RARE IN EUROPE: Non-alcoholic fatty liver disease,NON RARE IN EUROPE: Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency,NON RARE IN EUROPE: Obesity due to MC3R deficiency,NON RARE IN EUROPE: Paget disease of bone,NON RARE IN EUROPE: Parkinson disease,NON RARE IN EUROPE: Partial color blindness deutan type,NON RARE IN EUROPE: Partial color blindness protan type,NON RARE IN EUROPE: Patent arterial duct,NON RARE IN EUROPE: Primary adult open-angle glaucoma,NON RARE IN EUROPE: Primary bile acid malabsorption,NON RARE IN EUROPE: Primary ovarian failure,NON RARE IN EUROPE: Pseudoarylsulfatase A deficiency,NON RARE IN EUROPE: Psoriatic arthritis,NON RARE IN EUROPE: Recurrent acute pancreatitis,NON RARE IN EUROPE: Rheumatoid arthritis,NON RARE IN EUROPE: Specific language impairment,NON RARE IN EUROPE: Tourette syndrome,NON RARE IN EUROPE: Trimethylaminuria,NON RARE IN EUROPE: Ulcerative colitis,NON RARE IN EUROPE: Ventricular septal defect,NON RARE IN EUROPE: Vitiligo,NON RARE IN EUROPE: Wolff-Parkinson-White syndrome,Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome,Non-acquired panhypopituitarism,Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency,Non-degenerative Pontocerebellar Hypoplasia,Non-epidermolytic palmoplantar keratoderma,Non-hereditary retinoblastoma,Non-immune hydrops fetalis,Non-phenylketonuria hyperphenylalaninemia,Non-photosensitive trichothiodystrophy,Non-progressive cerebellar ataxia with intellectual disability,Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy,Non-seminomatous germ cell tumor of testis,Non-specific early-onset epileptic encephalopathy,Non-specific syndromic intellectual disability,Non-syndromic craniosynostosis,Non-syndromic male infertility due to sperm motility disorder,NONAKA MYOPATHY,NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY SUSCEPTIBILITY TO,Nonpecific severe ID,Nonspecific severe ID,Nonspherocytic hemolytic anemia due to hexokinase deficiency,Nonsyndromic autosomal-Recessive intellectual disability,Nonsyndromic deafness DFNB48,NONSYNDROMIC MENTAL RETARDATION,Noonan Syndrome,NOONAN SYNDROME 1,NOONAN SYNDROME 10,NOONAN SYNDROME 11,NOONAN SYNDROME 12,NOONAN SYNDROME 13,NOONAN SYNDROME 3,NOONAN SYNDROME 4,NOONAN SYNDROME 5,NOONAN SYNDROME 6,NOONAN SYNDROME 7,Noonan syndrome 8,NOONAN SYNDROME 9,NOONAN SYNDROME TYPE 3,Noonan syndrome type 6,Noonan syndrome with multiple lentigines,Noonan syndrome-like disorder with juvenile myelomonocytic leukemia,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2,Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia,Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia,Noonan-like syndrome with loose anagen hair,Normosmic congenital hypogonadotropic hypogonadism,NORRIE DISEASE,NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS,NOT IN OMIM,NPHP3-related Meckel-like syndrome,NR4A2-related developmental disorder monoallelic,NRROS-related Infantile-Onset Neurodegeneration with Intracranial Calcification,NSD2-related developmental disorder monoallelic,NTHL1-related attenuated familial adenomatous polyposis,Nuclear Envelopathy with Early Progeroid Appearance,NUDT2-related Developmental Disorder,Null pituitary adenoma,Null syndrome,NUT midline carcinoma,NYSTAGMUS 1 CONGENITAL X-LINKED,NYSTAGMUS 6 CONGENITAL X-LINKED,OAVS/Goldenhar syndrome,Obesity due to CEP19 deficiency,Obesity due to congenital leptin deficiency,Obesity due to leptin receptor gene deficiency,Obesity due to melanocortin 4 receptor deficiency,Obesity due to pro-opiomelanocortin deficiency,Obesity due to prohormone convertase-I deficiency,Obesity due to SIM1 deficiency,OBESITY EARLY-ONSET WITH ADRENAL INSUFFICIENCY AND RED HAIR,OBESITY HYPERPHAGIA AND DEVELOPMENTAL DELAY,OBESITY LEANNESS INCLUDED,Obsessive-compulsive disorder,OBSOLETE: Alpha-1-antichymotrypsin deficiency,occipital cortical malformations,Occipital encephalocele,Occipital horn syndrome,Occipital pachygyria and polymicrogyria,OCCULT MACULAR DYSTROPHY,Ochoa syndrome,OCLN-associated Band-like Calcification with Simplified Gyration and Polymicrogyria,Ocular albinism,Ocular albinism with congenital sensorineural deafness,Ocular anomalies-axonal neuropathy-developmental delay syndrome,Ocular cystinosis,Oculoauricular syndrome,Oculoauricular syndrome Schorderet type,Oculocerebrodental syndrome,Oculocerebrofacial syndrome Kaufman type,Oculocerebrorenal syndrome of Lowe,Oculocutaneous Albinism Type 1,Oculocutaneous albinism type 1A,Oculocutaneous albinism type 1B,Oculocutaneous albinism type 2,Oculocutaneous albinism type 3,Oculocutaneous albinism type 4,Oculocutaneous albinism type 6,Oculocutaneous albinism type 7,OCULOCUTANEOUS ALBINISM TYPE VIII,OCULODENTODIGITAL DYSPLASIA,OCULODENTODIGITAL DYSPLASIA AUTOSOMAL RECESSIVE,Oculoectodermal syndrome,Oculofaciocardiodental syndrome,OCULOMOTOR-ABDUCENS SYNKINESIS,Oculootodental syndrome,OCULOPHARYNGEAL MUSCULAR DYSTROPHY,OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1,OCULOPHARYNGODISTAL MYOPATHY 1,OCULOPHARYNGODISTAL MYOPATHY 2,OCULOSKELETODENTAL SYNDROME,Oculotrichoanal syndrome,ODC1-related developmental disorder monoallelic,ODONNELL-LURIA-RODAN SYNDROME,Odonto-onycho-dermal dysplasia,ODONTOCHONDRODYSPLASIA,ODONTOHYPOPHOSPHATASIA,Odontoleukodystrophy,ODONTOONYCHODERMAL DYSPLASIA,OGDEN SYNDROME,OGT-related developmental disorder hemizygous,OGT-related developmental disorder X-linked dominant,Oguchi disease,OGUCHI DISEASE 1,OGUCHI DISEASE 2,OHDO SYNDROME SBBYS VARIANT,OHDO SYNDROME X-LINKED,Okihiro syndrome due to 20q13 microdeletion,Okihiro syndrome due to a point mutation,OKT4 EPITOPE DEFICIENCY,OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME,Oligoarticular juvenile idiopathic arthritis,Oligoastrocytoma,Oligodendroglioma,Oligodontia,Oligodontia-cancer predisposition syndrome,Oligodontia-colorectal cancer syndrome,OLIVER-MCFARLANE SYNDROME,Ollier disease,Olmsted syndrome,Olmsted syndrome 1,OLMSTED SYNDROME 2,OLMSTED SYNDROME X-LINKED,OMENN SYNDROME,OMODYSPLASIA 1,OMODYSPLASIA 2,omodysplasia type 1 (OMOD1),Ondine syndrome,Oocyte maturation defect 1,OOCYTE MATURATION DEFECT 10,Oocyte maturation defect 2,OOCYTE MATURATION DEFECT 3,OOCYTE MATURATION DEFECT 4,OOCYTE MATURATION DEFECT 5,OOCYTE MATURATION DEFECT 6,OOCYTE MATURATION DEFECT 7,OOCYTE MATURATION DEFECT 8,OOCYTE MATURATION DEFECT 9,OPHTHALMOACROMELIC SYNDROME,OPHTHALMOPLEGIA EXTERNAL WITH RIB AND VERTEBRAL ANOMALIES,Opitz G/BBB Syndrome X-Linked,OPITZ GBBB SYNDROME TYPE I,OPITZ GBBB SYNDROME TYPE II,OPITZ-KAVEGGIA SYNDROME,Opsismodysplasia,OPTIC ATROPHY 1,OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA MENTAL RETARDATION AND SEIZURES,OPTIC ATROPHY 11,OPTIC ATROPHY 12,OPTIC ATROPHY 13 WITH RETINAL AND FOVEAL ABNORMALITIES,OPTIC ATROPHY 3 AUTOSOMAL DOMINANT,OPTIC ATROPHY 5,OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY,OPTIC ATROPHY 9,OPTIC ATROPHY WITH OR WITHOUT DEAFNESS OPHTHALMOPLEGIA MYOPATHY ATAXIA AND NEUROPATHY,Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome,Optic atrophy-intellectual disability syndrome,OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY,OPTIC NERVE HYPOPLASIA BILATERALOPTIC NERVE APLASIA BILATERAL INCLUDED,ORAL-FACIAL-DIGITAL SYNDROME TYPE 1,Oral-facial-digital syndrome with short stature and brachymesophalangy,ORNITHINE TRANSCARBAMYLASE DEFICIENCY,ORNITHINE TRANSCARBAMYLASE DEFICIENCY HYPERAMMONEMIA DUE TO,OROFACIAL CLEFT 10,OROFACIAL CLEFT 11,Orofacial cleft 15,OROFACIAL CLEFT 5,OROFACIAL CLEFT 6 SUSCEPTIBILITY TO,OROFACIAL CLEFT 8,Orofaciodigital syndrome,OROFACIODIGITAL SYNDROME I,OROFACIODIGITAL SYNDROME IV,Orofaciodigital syndrome type 1,Orofaciodigital syndrome type 14,Orofaciodigital syndrome type 2,Orofaciodigital syndrome type 3,Orofaciodigital syndrome type 4,Orofaciodigital syndrome type 5,Orofaciodigital syndrome type 6,OROFACIODIGITAL SYNDROME V,OROFACIODIGITAL SYNDROME VI,OROFACIODIGITAL SYNDROME XIV,Orofaciodigital syndrome XV,OROFACIODIGITAL SYNDROME XVI,OROFACIODIGITAL SYNDROME XVII,OROFACIODIGITAL SYNDROME XVIII,OROTIC ACIDURIA,OROTIC ACIDURIA TYPE 1,ORTHOSTATIC HYPOTENSION 1,ORTHOSTATIC HYPOTENSION 2,ORTHOSTATIC INTOLERANCE,OSSEOUS HETEROPLASIA PROGRESSIVE,OSTEOARTHRITIS SUSCEPTIBILITY 1,OSTEOARTHRITIS SUSCEPTIBILITY 2,OSTEOARTHRITIS SUSCEPTIBILITY 3,OSTEOARTHRITIS SUSCEPTIBILITY 5,OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA,OSTEOCHONDRODYSPLASIA BRACHYDACTYLY AND OVERLAPPING MALFORMED DIGITS,OSTEOCHONDRODYSPLASIA COMPLEX LETHAL SYMOENS-BARNES-GISTELINCK TYPE,Osteocraniostenosis,Osteofibrous dysplasia,OSTEOFIBROUS DYSPLASIA SUSCEPTIBILITY TO,OSTEOGENESIS IMPERFECTA,Osteogenesis imperfecta type 1,Osteogenesis imperfecta type 2,Osteogenesis imperfecta type 3,Osteogenesis imperfecta type 4,Osteogenesis imperfecta type 5,OSTEOGENESIS IMPERFECTA TYPE I,OSTEOGENESIS IMPERFECTA TYPE II,OSTEOGENESIS IMPERFECTA TYPE III,OSTEOGENESIS IMPERFECTA TYPE IV,OSTEOGENESIS IMPERFECTA TYPE IX,OSTEOGENESIS IMPERFECTA TYPE V,OSTEOGENESIS IMPERFECTA TYPE VI,OSTEOGENESIS IMPERFECTA TYPE VII,OSTEOGENESIS IMPERFECTA TYPE VIII,OSTEOGENESIS IMPERFECTA TYPE X,OSTEOGENESIS IMPERFECTA TYPE XI,OSTEOGENESIS IMPERFECTA TYPE XII,OSTEOGENESIS IMPERFECTA TYPE XIII,OSTEOGENESIS IMPERFECTA TYPE XIV,OSTEOGENESIS IMPERFECTA TYPE XIX,OSTEOGENESIS IMPERFECTA TYPE XV,OSTEOGENESIS IMPERFECTA TYPE XVI,OSTEOGENESIS IMPERFECTA TYPE XVII,OSTEOGENESIS IMPERFECTA TYPE XVIII,OSTEOGENESIS IMPERFECTA TYPE XX,OSTEOGENESIS IMPERFECTA TYPE XXI,OSTEOGENIC SARCOMA,OSTEOGLOPHONIC DYSPLASIA,Osteoglosphonic dysplasia,Osteomyelitis sterile multifocal with periostitis and pustulosis,OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS,Osteopathia striata-cranial sclerosis syndrome,OSTEOPETROSIS AUTOSOMAL DOMINANT 1,OSTEOPETROSIS AUTOSOMAL DOMINANT 2,OSTEOPETROSIS AUTOSOMAL DOMINANT 3,Osteopetrosis autosomal dominant type 1,OSTEOPETROSIS AUTOSOMAL RECESSIVE 1,OSTEOPETROSIS AUTOSOMAL RECESSIVE 2,OSTEOPETROSIS AUTOSOMAL RECESSIVE 3,OSTEOPETROSIS AUTOSOMAL RECESSIVE 4,OSTEOPETROSIS AUTOSOMAL RECESSIVE 5,OSTEOPETROSIS AUTOSOMAL RECESSIVE 6,OSTEOPETROSIS AUTOSOMAL RECESSIVE 7,OSTEOPETROSIS AUTOSOMAL RECESSIVE 8,OSTEOPETROSIS AUTOSOMAL RECESSIVE TYPE 3,Osteopetrosis with renal tubular acidosis,Osteopetrosis-hypogammaglobulinemia syndrome,OSTEOPOROSIS,OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME,OSTEOSARCOMA,Osteosclerosis-developmental delay-craniosynostosis syndrome,Osteosclerotic metaphyseal dysplasia,OTITIS MEDIA SUSCEPTIBILITY TO,Otodental syndrome,OTOFACIOCERVICAL SYNDROME,OTOFACIOCERVICAL SYNDROME 1,OTOFACIOCERVICAL SYNDROME 2,Otopalatodigital Syndrome,Otopalatodigital syndrome type 1,Otopalatodigital syndrome type 2,OTOPALATODIGITAL SYNDROME TYPE I,OTOPALATODIGITAL SYNDROME TYPE II,Otospondylomegaepiphyseal dysplasia,OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA AUTOSOMAL DOMINANT,OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA AUTOSOMAL RECESSIVE,Otulin-related auto inflammatory syndrome,OVALOCYTOSIS SOUTHEAST ASIAN,OVARIAN CANCER OVARIAN CANCER EPITHELIAL INCLUDED,OVARIAN DYSGENESIS 1,OVARIAN DYSGENESIS 2,OVARIAN DYSGENESIS 3,OVARIAN DYSGENESIS 4,OVARIAN DYSGENESIS 5,OVARIAN DYSGENESIS 6,OVARIAN DYSGENESIS 7,OVARIAN DYSGENESIS 8,OVARIAN HYPERSTIMULATION SYNDROME,OVARIOLEUKODYSTROPHY,Overgrowth-macrocephaly-facial dysmorphism syndrome,Overhydrated hereditary stomatocytosis,Oxoglutaric aciduria,Pachydermoperiostosis,PACHYGYRIA MICROCEPHALY DEVELOPMENTAL DELAY AND DYSMORPHIC FACIES WITH OR WITHOUT SEIZURES,Pachyonychia congenita,Pachyonychia congenita 1,Pachyonychia congenita 2,PACHYONYCHIA CONGENITA 3,PACHYONYCHIA CONGENITA 4,PAGANINI-MIOZZO SYNDROME,PAGET DISEASE OF BONE 2 EARLY-ONSET,PAGET DISEASE OF BONE 3,PAGET DISEASE OF BONE 5 JUVENILE-ONSET,PAGET DISEASE OF BONE 6,Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome,PALLISTER-HALL SYNDROME,PALLISTER-HALL-LIKE SYNDROME,PALMOPLANTAR CARCINOMA MULTIPLE SELF-HEALING,PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46XX SEX REVERSAL PALMOPLANTAR HYPERKERATOSIS AND TRUE HERMAPHRODITISM INCLUDED,PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1,Palmoplantar keratoderma and woolly hair,PALMOPLANTAR KERATODERMA BOTHNIAN TYPE,PALMOPLANTAR KERATODERMA EPIDERMOLYTIC,PALMOPLANTAR KERATODERMA I STRIATE FOCAL OR DIFFUSE,PALMOPLANTAR KERATODERMA NAGASHIMA TYPE,PALMOPLANTAR KERATODERMA NONEPIDERMOLYTIC,PALMOPLANTAR KERATODERMA NONEPIDERMOLYTIC FOCAL 1,PALMOPLANTAR KERATODERMA NONEPIDERMOLYTIC FOCAL 2,Palmoplantar keratoderma nonepidermolytic focal or diffuse,PALMOPLANTAR KERATODERMA PUNCTATE TYPE IA,Palmoplantar keratoderma-deafness syndrome,Palmoplantar keratoderma-esophageal carcinoma syndrome,Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome,Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome,PANCREATIC AGENESIS,PANCREATIC AGENESIS 1,PANCREATIC AGENESIS 2,Pancreatic agenesis diaphragmatic hernia and congenital heart defects,Pancreatic agenesis-holoprosencephaly syndrome,PANCREATIC AND CEREBELLAR AGENESIS,Pancreatic Cancer,PANCREATIC CANCER SUSCEPTIBILITY TO 1,PANCREATIC CANCER SUSCEPTIBILITY TO 2,PANCREATIC CANCER SUSCEPTIBILITY TO 3,PANCREATIC CANCER SUSCEPTIBILITY TO 4,PANCREATIC CANCER SUSCEPTIBILITY TO 5,Pancreatic hypoplasia-diabetes-congenital heart disease syndrome,Pancreatic insufficiency-anemia-hyperostosis syndrome,PANCREATIC LIPASE DEFICIENCY,PANCREATITIS HEREDITARY,Pancytopenia due to IKZF1 mutations,Pancytopenia-developmental delay syndrome,PANHYPOPITUITARISM X-LINKED,PANIC DISORDER 1,Papillary renal cell carcinoma,PAPILLOMA OF CHOROID PLEXUS,Papillon-Lefevre syndrome,PAPILLORENAL SYNDROME,PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA,PARAGANGLIOMAS 1,PARAGANGLIOMAS 2,Paragangliomas 3,PARAGANGLIOMAS 4,PARAGANGLIOMAS 5,PARAGANGLIOMAS 6,PARAGANGLIOMAS 7,PARAMYOTONIA CONGENITA OF VON EULENBURG,PARAOXONASE 1,Parastremmatic dwarfism,PARATHYROID CARCINOMA,PARIETAL FORAMINA 1,PARIETAL FORAMINA 2,Parietal foramina with clavicular hypoplasia,PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA,Paris-Trousseau thrombocytopenia,PARKES WEBER SYNDROME,PARKINSON DISEASE 1 AUTOSOMAL DOMINANT,PARKINSON DISEASE 11 AUTOSOMAL DOMINANT SUSCEPTIBILITY TO,PARKINSON DISEASE 13 AUTOSOMAL DOMINANT SUSCEPTIBILITY TO,PARKINSON DISEASE 14 AUTOSOMAL RECESSIVE,PARKINSON DISEASE 15 AUTOSOMAL RECESSIVE EARLY-ONSET,PARKINSON DISEASE 17,PARKINSON DISEASE 18 AUTOSOMAL DOMINANT SUSCEPTIBILITY TO,PARKINSON DISEASE 19A JUVENILE-ONSET,PARKINSON DISEASE 2 AUTOSOMAL RECESSIVE JUVENILE,Parkinson disease 20 early-onset,PARKINSON DISEASE 22 AUTOSOMAL DOMINANT,PARKINSON DISEASE 23 AUTOSOMAL RECESSIVE EARLY-ONSET,PARKINSON DISEASE 4 AUTOSOMAL DOMINANT,PARKINSON DISEASE 5 AUTOSOMAL DOMINANT SUSCEPTIBILITY TO,PARKINSON DISEASE 6 AUTOSOMAL RECESSIVE EARLY-ONSET,PARKINSON DISEASE 7 AUTOSOMAL RECESSIVE EARLY-ONSET,PARKINSON DISEASE 8 AUTOSOMAL DOMINANT,Parkinson disease 9,Parkinson disease late-onset,Parkinson-dementia complex of Guam,PARKINSON-DEMENTIA SYNDROME SUPRANUCLEAR PALSY PROGRESSIVE 1 ATYPICAL INCLUDED,Parkinsonian-pyramidal syndrome,PARKINSONISM WITH SPASTICITY X-LINKED,Parkinsonism-Dystonia Infantile,PARKINSONISM-DYSTONIA INFANTILE 1,PARKINSONISM-DYSTONIA INFANTILE 2,Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity,Paroxysmal exertion-induced dyskinesia,PAROXYSMAL EXTREME PAIN DISORDER,Paroxysmal kinesigenic dyskinesia,Paroxysmal nocturnal hemoglobinuria,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2,Paroxysmal non-kinesigenic dyskinesia,PAROXYSMAL NONKINESIGENIC DYSKINESIA 1,PAROXYSMAL NONKINESIGENIC DYSKINESIA 3 WITH OR WITHOUT GENERALIZED EPILEPSY,Partial androgen insensitivity syndrome,Partial atrioventricular septal defect,Partial chromosome Y deletion,Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome,Partial hydatidiform mole,Partial pancreatic agenesis,Partington syndrome,PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME,PATENT DUCTUS ARTERIOSUS 2,PATENT DUCTUS ARTERIOSUS 3,Paternal uniparental disomy of chromosome 6,PBX1-related developmental disorder monoallelic,PCBP2-related developmental disorder monoallelic,PCNA-related progressive neurodegenerative photosensitivity syndrome,PDE4D haploinsufficiency syndrome,Pediatric hepatocellular carcinoma,Pediatric multiple sclerosis,Pediatric systemic lupus erythematosus,PEELING SKIN SYNDROME 1,PEELING SKIN SYNDROME 2,Peeling skin syndrome 3,PEELING SKIN SYNDROME 4,PEELING SKIN SYNDROME 5,PEELING SKIN SYNDROME 6,Peeling skin syndrome type A,Peeling skin syndrome type B,PEELING SKIN WITH LEUKONYCHIA ACRAL PUNCTATE KERATOSES CHEILITIS AND KNUCKLE PADS,Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome,PEHO Like condition,PEHO syndrome,PEHO-like syndrome,PELGER-HUET ANOMALY,PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES,PELIZAEUS-MERZBACHER DISEASE,Pelizaeus-Merzbacher disease classic form,Pelizaeus-Merzbacher disease connatal form,Pelizaeus-Merzbacher disease in female carriers,Pelizaeus-Merzbacher disease transitional form,Pelizaeus-Merzbacher-like disease due to AIMP1 mutation,Pelizaeus-Merzbacher-like disease due to GJC2 mutation,Pelizaeus-Merzbacher-like disease due to HSPD1 mutation,Pelviscapular dysplasia,PENDRED SYNDROME,Pentosuria,PEPSINOGEN 3 GROUP I,PERCHING syndrome,Perinatal lethal hypophosphatasia,PERIODIC FEVER FAMILIAL AUTOSOMAL DOMINANT,PERIODIC FEVER IMMUNODEFICIENCY AND THROMBOCYTOPENIA SYNDROME,PERIODIC FEVER MENSTRUAL CYCLE-DEPENDENT,Periodic fever-infantile enterocolitis-autoinflammatory syndrome,Periodic paralysis with later-onset distal motor neuropathy,Periodic paralysis with transient compartment-like syndrome,Periodontal Ehlers-Danlos syndrome,PERIODONTITIS AGGRESSIVE 1,PERIPHERAL DEMYELINATING NEUROPATHY CENTRAL DYSMYELINATING LEUKODYSTROPHY WAARDENBURG SYNDROME AND HIRSCHSPRUNG DISEASE,PERIPHERAL DEMYELINATING NEUROPATHY CENTRAL DYSMYELINATION WAARDENBURG SYNDROME AND HIRSCHSPRUNG DISEASE,Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease,PERIPHERAL NEUROPATHY AUTOSOMAL RECESSIVE WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT,PERIPHERAL NEUROPATHY MYOPATHY HOARSENESS AND HEARING LOSS,Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome,Peripheral primitive neuroectodermal tumor,Periventricular Heterotopia,Periventricular Heterotopia with Microcephaly,Periventricular Heterotopia with Microcephaly autosomal recessive,periventricular neuronal heterotopia,Periventricular nodular heterotopia,Periventricular nodular heterotopia 1,Periventricular nodular heterotopia 6,PERIVENTRICULAR NODULAR HETEROTOPIA 7,PERIVENTRICULAR NODULAR HETEROTOPIA 8,PERIVENTRICULAR NODULAR HETEROTOPIA 9,Periventricular nodular heterotopia with ID cleft palate and 2.3 toe syndactyly,Perlman syndrome,Permanent neonatal diabetes mellitus,Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome,PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY,Peroxisomal fatty acyl-coa reductase 1 disorder,PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER),PEROXISOME BIOGENESIS DISORDER 10B,PEROXISOME BIOGENESIS DISORDER 11A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 11B,PEROXISOME BIOGENESIS DISORDER 12A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER),PEROXISOME BIOGENESIS DISORDER 14B,PEROXISOME BIOGENESIS DISORDER 1A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 1B,PEROXISOME BIOGENESIS DISORDER 2A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 2B,PEROXISOME BIOGENESIS DISORDER 3A ZELLWEGER,Peroxisome biogenesis disorder 3B,PEROXISOME BIOGENESIS DISORDER 4A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 4B,PEROXISOME BIOGENESIS DISORDER 5A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 5B,PEROXISOME BIOGENESIS DISORDER 6A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 6B,PEROXISOME BIOGENESIS DISORDER 7A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 7B,PEROXISOME BIOGENESIS DISORDER 8A ZELLWEGER,PEROXISOME BIOGENESIS DISORDER 8B,PEROXISOME BIOGENESIS DISORDER 9B,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 1,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 11,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 12,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 13,Peroxisome biogenesis disorder complementation group 3,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 4,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 5,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 7,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 9,PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP K,PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-ALPHA,Perrault syndrome,PERRAULT SYNDROME 1,PERRAULT SYNDROME 2,PERRAULT SYNDROME 3,Perrault syndrome 4,PERRAULT SYNDROME 5,PERRAULT SYNDROME 6,PERRY SYNDROME,Persistent hyperplastic primary vitreous,Persistent hyperplastic primary vitreous autosomal recessive,Persistent Hypotonia Encephalopathy Growth Retardation and Severe Intellectual Disability,Persistent Mullerian duct syndrome,PERSISTENT MULLERIAN DUCT SYNDROME TYPES I AND II,Persistent polyclonal B-cell lymphocytosis,PETERS ANOMALY,Peters plus syndrome,PETERS-PLUS SYNDROME,PETTIGREW SYNDROME,Peutz-Jeghers Syndrome,PFEIFFER SYNDROME,Pfeiffer syndrome type 1,Pfeiffer syndrome type 2,Pfeiffer syndrome type 3,PGM1-CDG,PGM3-CDG,PHACTR1-associated neurodevelopment disorder,Phakomatosis cesioflammea,Phakomatosis cesiomarmorata,Phakomatosis pigmentokeratotica,Phelan-McDermid syndrome,Phenocopy of Proximal 1p36 Deletions,PHENYLKETONURIA,Pheochromocytoma,Phocomelia Schinzel type,Phosphoenolpyruvate carboxykinase deficiency,PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY CYTOSOLIC,PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY MITOCHONDRIAL,PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY,PHOSPHOGLYCERATE KINASE 1 DEFICIENCY,Phosphohydroxylysinuria,PHOSPHOLIPID TRANSFER PROTEIN,PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY,PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY,Phosphoserine aminotransferase deficiency infantile/juvenile form,PHOSPHOSERINE PHOSPHATASE DEFICIENCY,PICK DISEASE OF BRAIN,PIDD1-related neurodevelopmental disorder,Piebald trait,PIEBALDISM,PIERPONT SYNDROME,PIERRE ROBIN SEQUENCE,PIERSON SYNDROME,PIGK-associated Neurodevelopmental Syndrome,Pigmentary disorder reticulate with systemic manifestations X-linked,Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome,PIGMENTED NODULAR ADRENOCORTICAL DISEASE PRIMARY 1,PIGMENTED NODULAR ADRENOCORTICAL DISEASE PRIMARY 2,PIGMENTED NODULAR ADRENOCORTICAL DISEASE PRIMARY 3,PIGMENTED NODULAR ADRENOCORTICAL DISEASE PRIMARY 4,PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY,Pigmented paravenous retinochoroidal atrophy,PILAROWSKI-BJORNSSON SYNDROME,Pilomatrixoma,Pilomyxoid astrocytoma,PINEAL HYPERPLASIA INSULIN-RESISTANT DIABETES MELLITUS AND SOMATIC ABNORMALITIES,Pitt Hopkins 2,PITT-HOPKINS SYNDROME,Pitt-Hopkins-like syndrome,Pitt-Hopkins-like syndrome 1,Pitt-Hopkins-like syndrome 2,PITUITARY ADENOMA 1 MULTIPLE TYPES,PITUITARY ADENOMA 2 GROWTH HORMONE-SECRETING,PITUITARY ADENOMA 3 MULTIPLE TYPES,PITUITARY ADENOMA 4 ACTH-SECRETING,PITUITARY ADENOMA 5 MULTIPLE TYPES,Pituitary Dwarfism II,Pituitary gigantism,PITUITARY HORMONE DEFICIENCY COMBINED 1,PITUITARY HORMONE DEFICIENCY COMBINED 2,PITUITARY HORMONE DEFICIENCY COMBINED 3,PITUITARY HORMONE DEFICIENCY COMBINED 4,PITUITARY HORMONE DEFICIENCY COMBINED 6,pituitary hormone deficiency combined type 3,Pituitary stalk interruption syndrome,Pityriasis rubra pilaris,PLAA-associated neurodevelopmental disorder,Plaque-form urticaria pigmentosa,PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS,PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY,PLASMINOGEN DEFICIENCY TYPE I LIGNEOUS CONJUNCTIVITIS INCLUDED,PLATELET DISORDER FAMILIAL WITH ASSOCIATED MYELOID MALIGNANCY,PLATELET GLYCOPROTEIN IV DEFICIENCY,PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY,Platyspondylic dysplasia Torrance type,PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA TORRANCE TYPE,Platyspondyly with amelogenesis imperfecta,PLCG2-associated antibody deficiency and immune dysregulation,PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement,Plectin-related  limb-girdle muscular dystrophy R17,Pleomorphic salivary gland adenoma,PLEUROPULMONARY BLASTOMA,Pleuropulmonary blastoma familial tumor susceptibility syndrome,PLG-related hereditary angioedema with normal C1Inh,PLIN1-related familial partial lipodystrophy,PMM2-CDG,PMP2-related Charcot-Marie-Tooth disease type 1,PMP22-RAI1 contiguous gene duplication syndrome,Pneumothorax primary spontaneous,PNPLA6-related Disorder,POGLUT1-related  limb-girdle muscular dystrophy R21,Poikiloderma hereditary fibrosing with tendon contractures myopathy and pulmonary fibrosis,POIKILODERMA WITH NEUTROPENIA,POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME,POLR1C-related Leukodystrophy,POLR3B-related neurodevelopmental disorder,POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,POLYCYSTIC KIDNEY DISEASE 2 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,POLYCYSTIC KIDNEY DISEASE 5,POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,POLYCYSTIC KIDNEY DISEASE AUTOSOMAL RECESSIVE,Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2,POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS,POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS,POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS,POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS,POLYCYTHEMIA VERA,Polydactyly of a biphalangeal thumb,Polydactyly of a triphalangeal thumb,POLYDACTYLY POSTAXIAL TYPE A1,POLYDACTYLY POSTAXIAL TYPE A10,POLYDACTYLY POSTAXIAL TYPE A6,POLYDACTYLY POSTAXIAL TYPE A7,POLYDACTYLY POSTAXIAL TYPE A8,POLYDACTYLY POSTAXIAL TYPE A9,POLYDACTYLY PREAXIAL I,POLYDACTYLY PREAXIAL II,POLYDACTYLY PREAXIAL IV,Polyendocrine-polyneuropathy syndrome,POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY,POLYGLUCOSAN BODY MYOPATHY 2,Polyglucosan body myopathy type 1,Polyglucosan body myopathy type 2,POLYGLUCOSAN BODY NEUROPATHY ADULT FORM,POLYHYDRAMNIOS MEGALENCEPHALY AND SYMPTOMATIC EPILEPSY,Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome,Polymerase proofreading-related adenomatous polyposis,Polymicrogyria,POLYMICROGYRIA AND CORPUS CALLOSUM AGENESIS,POLYMICROGYRIA ASYMMETRIC,POLYMICROGYRIA BILATERAL FRONTOPARIETAL,Polymicrogyria bilateral perisylvian autosomal recessive,Polymicrogyria bilateral temporooccipital,Polymicrogyria due to TUBB2B mutation,POLYMICROGYRIA PERISYLVIAN WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS,POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA,POLYMICROGYRIA WITH OR WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME,Polyneuropathy hearing loss ataxia retinitis pigmentosa and cataract,Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome,Polyostotic fibrous dysplasia,POLYPOSIS SYNDROME HEREDITARY MIXED 2,POLYSUBSTANCE ABUSE SUSCEPTIBILITY TO,Polysyndactyly,Polyvalvular heart disease syndrome,POMGNT1-related  limb-girdle muscular dystrophy R15,POMT1-related  limb-girdle muscular dystrophy R11,POMT2-related  limb-girdle muscular dystrophy R14,Pontine autosomal dominant microangiopathy with leukoencephalopathy,Pontocerebellar hypoplasia,Pontocerebellar hypoplasia and microcephaly,Pontocerebellar Hypoplasia and Progressive Microcephaly,PONTOCEREBELLAR HYPOPLASIA HYPOTONIA AND RESPIRATORY INSUFFICIENCY SYNDROME NEONATAL LETHAL,Pontocerebellar hypoplasia type 1,Pontocerebellar hypoplasia type 10,PONTOCEREBELLAR HYPOPLASIA TYPE 11,PONTOCEREBELLAR HYPOPLASIA TYPE 12,PONTOCEREBELLAR HYPOPLASIA TYPE 13,PONTOCEREBELLAR HYPOPLASIA TYPE 1A,PONTOCEREBELLAR HYPOPLASIA TYPE 1B,PONTOCEREBELLAR HYPOPLASIA TYPE 1C,PONTOCEREBELLAR HYPOPLASIA TYPE 1D,Pontocerebellar hypoplasia type 2,Pontocerebellar Hypoplasia Type 2 and Type 4,PONTOCEREBELLAR HYPOPLASIA TYPE 2A,PONTOCEREBELLAR HYPOPLASIA TYPE 2B,PONTOCEREBELLAR HYPOPLASIA TYPE 2C,PONTOCEREBELLAR HYPOPLASIA TYPE 2D,Pontocerebellar hypoplasia type 2e,PONTOCEREBELLAR HYPOPLASIA TYPE 2F,Pontocerebellar hypoplasia type 3,Pontocerebellar hypoplasia type 4,PONTOCEREBELLAR HYPOPLASIA TYPE 5,Pontocerebellar hypoplasia type 6,Pontocerebellar hypoplasia type 7,Pontocerebellar hypoplasia type 8,Pontocerebellar hypoplasia type 9,POPLITEAL PTERYGIUM SYNDROME,Popliteal pterygium syndrome lethal type,PORENCEPHALY 1,Porencephaly 2,Porencephaly-microcephaly-bilateral congenital cataract syndrome,Poretti-boltshauser syndrome,POROKERATOSIS 1 MULTIPLE TYPES,POROKERATOSIS 3 MULTIPLE TYPES,Porokeratosis 7 multiple types,POROKERATOSIS 8 DISSEMINATED SUPERFICIAL ACTINIC TYPE,POROKERATOSIS 9 MULTIPLE TYPES,Porokeratosis of Mibelli,Porokeratotic eccrine ostial and dermal duct nevus,PORPHYRIA ACUTE HEPATIC,PORPHYRIA ACUTE INTERMITTENT,PORPHYRIA CONGENITAL ERYTHROPOIETIC,PORPHYRIA CUTANEA TARDA,Porphyria due to ALA dehydratase deficiency,PORPHYRIA VARIEGATA,Portal hypertension noncirrhotic,Postaxial acrofacial dysostosis,Postaxial Polydactyly Type A,Postaxial polydactyly type B,Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome,Posterior Amelia with Pelvic and Pulmonary Hypoplasia,POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA,Posterior column ataxia-retinitis pigmentosa syndrome,Posterior hypospadias,Posterior polymorphous corneal dystrophy,Posterior urethral valve,Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome,Posteriorly predominant pachygyria and severe microcephaly,Postnatal microcephaly hypomyelination and reduced cerebral white-Matter volume,Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome,Postsynaptic congenital myasthenic syndromes,Postural orthostatic tachycardia syndrome due to NET deficiency,POTOCKI-LUPSKI SYNDROME,Potocki-Shaffer syndrome,POU1F1-Related Combined Pituitary Hormone Deficiency,PPARG-related familial partial lipodystrophy,PPIL1-related Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly,PPM1D syndrome,PPP1R12A-related Holoprosencephaly Spectrum and Urogenital Malformations,PPP1R13L-related dilated cardiomyopathy,PPP1R21-related neurodevelopmental disorder,PRADER-WILLI SYNDROME,Prader-Willi syndrome due to imprinting mutation,Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2,Prader-Willi syndrome due to translocation,PRDM15-related renal and neurodevelopmental disorder,PREAXIAL DEFICIENCY POSTAXIAL POLYDACTYLY AND HYPOSPADIAS,PRECOCIOUS PUBERTY CENTRAL 1,Precocious puberty central 2,PRECOCIOUS PUBERTY MALE-LIMITED,Precursor B-cell acute lymphoblastic leukemia,Precursor T-cell acute lymphoblastic leukemia,Predisposition to invasive fungal disease due to CARD9 deficiency,Predisposition to severe viral infection due to IRF7 deficiency,Preeclampsia,PREECLAMPSIA/ECLAMPSIA 1,PREECLAMPSIA/ECLAMPSIA 4,PREECLAMPSIA/ECLAMPSIA 5,PREGNANCY LOSS RECURRENT SUSCEPTIBILITY TO 1,PREGNANCY LOSS RECURRENT SUSCEPTIBILITY TO 2,PREGNANCY LOSS RECURRENT SUSCEPTIBILITY TO 3,PREIMPLANTATION EMBRYONIC LETHALITY 1,PREIMPLANTATION EMBRYONIC LETHALITY 2,PREKALLIKREIN DEFICIENCY,PREMATURE AGING SYNDROME PENTTINEN TYPE,PREMATURE CHROMATID SEPARATION TRAIT,PREMATURE OVARIAN FAILURE 1,Premature ovarian failure 10,Premature ovarian failure 11,Premature ovarian failure 12,PREMATURE OVARIAN FAILURE 13,PREMATURE OVARIAN FAILURE 14,PREMATURE OVARIAN FAILURE 15,PREMATURE OVARIAN FAILURE 16,PREMATURE OVARIAN FAILURE 17,PREMATURE OVARIAN FAILURE 18,PREMATURE OVARIAN FAILURE 19,PREMATURE OVARIAN FAILURE 2A,PREMATURE OVARIAN FAILURE 2B,PREMATURE OVARIAN FAILURE 3,Premature ovarian failure 5,PREMATURE OVARIAN FAILURE 6,Premature ovarian failure 7,Premature ovarian failure 8,Premature ovarian failure 9,PREMATURE OVARIAN FAILURE SYNDROME TYPE 1,Prenatal benign hypophosphatasia,Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures,Prenatal-onset spinal muscular atrophy with congenital bone fractures,Presynaptic congenital myasthenic syndromes,PRETERM PREMATURE RUPTURE OF THE MEMBRANES,PRIM1-related Primordial Dwarfism,Primary aldosteronism seizures and neurologic abnormalities,Primary Autosomal Recessive Microcephaly,Primary biliary cholangitis,Primary CD59 deficiency,PRIMARY CILARY DYSKINESIA,Primary ciliary dyskineasia,Primary ciliary dyskinesia,Primary Ciliary Dyskinesia and Male Infertility,Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms.,Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects,Primary ciliary dyskinesia with central-Complex defects,Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization,PRIMARY CILIARY DYSKINESIA-22,Primary ciliary dyskinesia-retinitis pigmentosa syndrome,Primary ciliary dysplasia,Primary cillary dyskineasia,PRIMARY CONGENITAL GLAUCOMA TYPE 3A,Primary cutaneous anaplastic large cell lymphoma,Primary dystonia DYT2 type,Primary dystonia DYT27 type,Primary dystonia DYT4 type,Primary dystonia DYT6 type,Primary erythromelalgia,PRIMARY FAILURE OF TOOTH ERUPTION,Primary familial polycythemia,Primary Fanconi renotubular syndrome,Primary hyperaldosteronism-seizures-neurological abnormalities syndrome,Primary hypereosinophilic syndrome,Primary hyperoxaluria type 1,Primary hyperoxaluria type 2,Primary hyperoxaluria type 3,Primary hypomagnesemia with secondary hypocalcemia,Primary immunodeficiency syndrome due to LAMTOR2 deficiency,Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency,Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection,Primary intraosseous venous malformation,Primary lateral sclerosis,PRIMARY LATERAL SCLEROSIS JUVENILE,Primary mediastinal large B-cell lymphoma,Primary microcephaly,Primary Microcephaly and Disturbed Centrosomal Function,Primary microcephaly cortical malformation and epileptic encephalopathy,Primary Microcephaly or macrocephaly with developmental delay,Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome,Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome,Primary myelofibrosis,Primary peritoneal carcinoma,Primary pigmented nodular adrenocortical disease,Primary sclerosing cholangitis,Primordial Dwarfism,PRIMORDIAL DWARFISM SECKEL SYNDROME 8,Primrose syndrome,PRKACA-related Multiple Congenital Malformation Syndrome,PRKACB-related Multiple Congenital Malformation Syndrome,PRKAR1B-related developmental disorder,PRKAR1B-related neurodegenerative dementia with intermediate filaments,Progeroid and marfanoid aspect-lipodystrophy syndrome,Progeroid features-hepatocellular carcinoma predisposition syndrome,PROGEROID SYNDROME,Progeroid syndrome Petty type,PROGESTERONE RESISTANCE,Progressive autosomal recessive ataxia-deafness syndrome,Progressive cerebella-cerebral atrophy type 2,Progressive cerebello-cerebral atrophy,Progressive Childhood Encephalopathy and Golgi Dysfunction,Progressive cone dystrophy,Progressive encephalopathy with leukodystrophy due to DECR deficiency,Progressive epilepsy-intellectual disability syndrome Finnish type,Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL DOMINANT 1,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL DOMINANT 2,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL DOMINANT 3,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL DOMINANT 5,Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal dominant 6,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL RECESSIVE 1,Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive 2,Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive 3,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL RECESSIVE 4,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL RECESSIVE 5,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONSAUTOSOMAL DOMINANT 4,Progressive external ophthalmoplegia-myopathy-emaciation syndrome,PROGRESSIVE FAMILIAL HEART BLOCK TYPE IA,PROGRESSIVE FAMILIAL HEART BLOCK TYPE IB,Progressive familial intrahepatic cholestasis type 1,Progressive familial intrahepatic cholestasis type 2,Progressive familial intrahepatic cholestasis type 3,Progressive familial intrahepatic cholestasis type 4,Progressive familial intrahepatic cholestasis type 5,Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome,Progressive myoclonic epilepsy type 3,Progressive myoclonic epilepsy type 5,Progressive myoclonic epilepsy type 6,Progressive myoclonic epilepsy type 7,Progressive myoclonic epilepsy type 8,Progressive myoclonic epilepsy type 9,Progressive myoclonic epilepsy with dystonia,Progressive neurological disorder and regression of developmental milestones,Progressive non-fluent aphasia,Progressive osseous heteroplasia,Progressive polyneuropathy with bilateral striatal necrosis,Progressive pseudorheumatoid arthropathy of childhood,Progressive pseudorheumatoid dysplasia,Progressive retinal dystrophy due to retinol transport defect,Progressive scapulohumeroperoneal distal myopathy,Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome,Progressive Spastic Ataxia and Hypomyelination,PROGRESSIVE SPONDYLOEPIMETAPHYSEAL DYSPLASIA,Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome,Progressive supranuclear palsy - corticobasal syndrome,Progressive supranuclear palsy-parkinsonism syndrome,Progressive supranuclear palsy-progressive non-fluent aphasia syndrome,Progressive supranuclear palsy-pure akinesia with gait freezing syndrome,Progressive symmetric erythrokeratodermia,Prolactinoma,PROLIDASE DEFICIENCY,Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome,Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome,PROLONGED ELECTRORETINAL RESPONSE SUPPRESSION,PROP1-Related Combined Pituitary Hormone Deficiency,Properdin deficiency,PROPERDIN DEFICIENCY X-LINKED,PROPIONIC ACIDEMIA,PROPROTEIN CONVERTASE 1/3 DEFICIENCY,Prostate Cancer,PROSTATE CANCER HEREDITARY 1,PROSTATE CANCER HEREDITARY 12,PROSTATE CANCER HEREDITARY 13,PROSTATE CANCER HEREDITARY 2,Prostate cancer hereditary 9,PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY,Proteasome-associated autoinflammatory syndrome,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 4,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5,PROTEIN Z DEFICIENCY,PROTEINURIA CHRONIC BENIGN,PROTEINURIA LOW MOLECULAR WEIGHT WITH HYPERCALCIURIA AND NEPHROCALCINOSIS,Proteus syndrome,Proteus-like syndrome,PROTHROMBIN DEFICIENCY CONGENITAL,Protoplasmic astrocytoma,PROTOPORPHYRIA ERYTHROPOIETIC 1,PROTOPORPHYRIA ERYTHROPOIETIC 2,PROTOPORPHYRIA ERYTHROPOIETIC X-LINKED,Proximal 16p11.2 microdeletion syndrome,Proximal myopathy with extrapyramidal signs,Proximal myopathy with focal depletion of mitochondria,Proximal myotonic myopathy,PROXIMAL RENAL TUBULAR ACIDOSIS WITH OCULAR ABNORMALITIES,Proximal spinal muscular atrophy type 1,Proximal spinal muscular atrophy type 2,Proximal spinal muscular atrophy type 3,Proximal spinal muscular atrophy type 4,Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance,Proximal symphalangism,PrP systemic amyloidosis,PRPF8-related developmental disorder monoallelic,Prune belly syndrome,PRUNE1-related neurological syndrome,Pseudo von Willebrand disease,PSEUDO-TORCH SYNDROME 1,PSEUDO-TORCH SYNDROME 2,PSEUDO-TORCH SYNDROME 3,PSEUDOACHONDROPLASIA,PSEUDOFOLLICULITIS BARBAE,PSEUDOHYPERKALEMIA FAMILIAL 2 DUE TO RED CELL LEAK,Pseudohypoaldosteronism type 2B,Pseudohypoaldosteronism type 2C,Pseudohypoaldosteronism type 2D,Pseudohypoaldosteronism type 2E,PSEUDOHYPOALDOSTERONISM TYPE I AUTOSOMAL DOMINANT,PSEUDOHYPOALDOSTERONISM TYPE I AUTOSOMAL RECESSIVE,PSEUDOHYPOALDOSTERONISM TYPE IIB,PSEUDOHYPOALDOSTERONISM TYPE IIC,PSEUDOHYPOALDOSTERONISM TYPE IID,PSEUDOHYPOALDOSTERONISM TYPE IIE,Pseudohypoparathyroidism type 1A,Pseudohypoparathyroidism type 1B,Pseudohypoparathyroidism type 1C,PSEUDOHYPOPARATHYROIDISM TYPE IA,PSEUDOHYPOPARATHYROIDISM TYPE IB,PSEUDOHYPOPARATHYROIDISM TYPE IC,Pseudohypoparathyroidism-like disorder,PSEUDOPSEUDOHYPOPARATHYROIDISM,PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS,Pseudoxanthoma elasticum,PSEUDOXANTHOMA ELASTICUM FORME FRUSTEPSEUDOXANTHOMA ELASTICUM HETEROZYGOUS INCLUDED,Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency,Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa,Pseudoxanthomatous diffuse cutaneous mastocytosis,PSMC5-related developmental disorder monoallelic,PSORIASIS 1 SUSCEPTIBILITY TO,PSORIASIS 13 SUSCEPTIBILITY TO,PSORIASIS 14 PUSTULAR,PSORIASIS 15 PUSTULAR SUSCEPTIBILITY TO,Psoriasis 2,PSORIASIS 7 SUSCEPTIBILITY TO,PSORIATIC ARTHRITIS SUSCEPTIBILITY TOPSORIATIC ARTHRITIS SUSCEPTIBILITY TO 1 INCLUDED,Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome,Psychomotor retardation epilepsy and craniofacial dysmorphism,Pten Hamartoma Tumor Syndrome,Pterin-4 alpha-carbinolamine dehydratase deficiency,PTOSIS HEREDITARY CONGENITAL 1,PUF60 syndrome,PULMONARY ALVEOLAR MICROLITHIASIS,Pulmonary arterial hypertension associated with connective tissue disease,Pulmonary artery and lung hypoplasia agonadism omphalocele diaphragmatic defects hypoplastic left heart and scimitar syndrome,Pulmonary capillary hemangiomatosis,PULMONARY DISEASE CHRONIC OBSTRUCTIVE,Pulmonary fibrosis and/or bone marrow failure telomere-related 1,PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE TELOMERE-RELATED 3,PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE TELOMERE-RELATED 4,PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE TELOMERE-RELATED 5,PULMONARY FIBROSIS IDIOPATHIC,PULMONARY HYPERTENSION NEONATAL SUSCEPTIBILITY TO,PULMONARY HYPERTENSION PRIMARY 1,PULMONARY HYPERTENSION PRIMARY 2,PULMONARY HYPERTENSION PRIMARY 3,PULMONARY HYPERTENSION PRIMARY 4,PULMONARY VENOOCCLUSIVE DISEASE,PULMONARY VENOOCCLUSIVE DISEASE 1 AUTOSOMAL DOMINANT,PULMONARY VENOOCCLUSIVE DISEASE 2 AUTOSOMAL RECESSIVE,Pulverulent cataract,Punctate palmoplantar keratoderma type 1,PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation,Pure hair and nail ectodermal dysplasia,PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY,Pustulosis palmaris et plantaris,PYCNODYSOSTOSIS,PYCR1-related DeBarsy syndrome,PYCR2-related microcephaly-progressive leukoencephalopathy,PYLE DISEASE,Pyogenic arthritis-pyoderma gangrenosum-acne syndrome,PYOGENIC STERILE ARTHRITIS PYODERMA GANGRENOSUM AND ACNE,Pyridoxal phosphate-responsive seizures,PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY,Pyridoxine-dependent epilepsy,PYROPOIKILOCYTOSIS HEREDITARY,PYRUVATE CARBOXYLASE DEFICIENCY,Pyruvate carboxylase deficiency benign type,Pyruvate carboxylase deficiency infantile type,Pyruvate carboxylase deficiency severe neonatal type,PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY,Pyruvate Dehydrogenase E1-Alpha Deficiency in females,PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY,PYRUVATE DEHYDROGENASE E2 DEFICIENCY,Pyruvate dehydrogenase E3 deficiency,PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY,Pyruvate dehydrogenase phosphatase deficiency,PYRUVATE KINASE DEFICIENCY OF RED CELLS,QRICH1 syndrome,QRICH1-related intellectual disability-chondrodysplasia syndrome,QRSL1-related combined oxidative phosphorylation defect,QUEBEC PLATELET DISORDER,Question mark ears isolated,RAB14-related developmental disorder monoallelic,RABSON-MENDENHALL SYNDROME,Radial hemimelia,RADIN BLOOD GROUP ANTIGEN,Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome,Radiohumeral fusions with other skeletal and craniofacial anomalies,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1,Radioulnar synostosis with amegakaryocytic thrombocytopenia 2,RAFIQ SYNDROME,RAHMAN SYNDROME,Raine syndrome,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 1,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 2,RALGAPA1-related neurodevelopmental disorder,Ramon syndrome,RAP1B-related developmental disorder,RAPADILINO SYNDROME,RAPH BLOOD GROUP SYSTEM,Rapid-Onset Dystonia-Parkinsonism,RAPP-HODGKIN SYNDROME,Rare isolated myopia,RARS-related autosomal recessive hypomyelinating leukodystrophy,RARS1 related hypomyelinating leukodystrophy,RAS-associated autoimmune leukoproliferative disease,RAS-associated autoimmune leukoproliferative disorder,Rasopathy with developmental delay short stature and sparse slow-growing hair,RAYNAUD-CLAES SYNDROME,RBFOX1-related neurodevelopmental disorder,Recessive dystrophic epidermolysis bullosa inversa,Recessive gain of function causing increased interferon signalling,Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome,Recessive mitochondrial ataxia syndrome,Recessive Neurodevelopmental Syndrome,Recessive Spondylocarpotarsal Synostosis Syndrome,Recessive X-linked ichthyosis,RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1,Recurrent infection due to specific granule deficiency,Recurrent infections associated with rare immunoglobulin isotypes deficiency,Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome,Recurrent Neisseria infections due to factor D deficiency,Reducing body myopathy,REDUCING BODY MYOPATHY X-LINKED 1A SEVERE WITH INFANTILE OR EARLYCHILDHOOD ONSET,REDUCING BODY MYOPATHY X-LINKED 1B WITH LATE CHILDHOOD OR ADULTONSET,Refractory anemia,Refractory anemia with excess blasts,Refsum disease,REFSUM DISEASE CLASSIC,Regressive spondylometaphyseal dysplasia,Reis-Bucklers corneal dystrophy,RELA fusion-positive ependymoma,REN-related autosomal dominant tubulointerstitial kidney disease,RENAL AGENESIS,Renal agenesis bilateral,Renal agenesis unilateral,RENAL CELL CARCINOMA NONPAPILLARY,Renal cell carcinoma papillary 1,RENAL CELL CARCINOMA Xp11-ASSOCIATED,Renal coloboma syndrome,RENAL CYSTS AND DIABETES SYNDROME,Renal dysplasia bilateral,RENAL DYSPLASIA CYSTIC SUSCEPTIBILITY TO,Renal dysplasia unilateral,RENAL GLUCOSURIA,RENAL HYPODYSPLASIA/APLASIA 1,Renal hypodysplasia/aplasia 2,RENAL HYPODYSPLASIA/APLASIA 3,Renal Hypomagnesemia Refractory Seizures and Intellectual Disability,Renal hypoplasia bilateral,Renal pseudohypoaldosteronism type 1,RENAL TUBULAR ACIDOSIS DISTAL 1,RENAL TUBULAR ACIDOSIS DISTAL 2 WITH PROGRESSIVE SENSORINEURAL HEARING LOSS,RENAL TUBULAR ACIDOSIS DISTAL 3 WITH OR WITHOUT SENSORINEURAL HEARING LOSS,RENAL TUBULAR ACIDOSIS DISTAL 4 WITH HEMOLYTIC ANEMIA,Renal tubular acidosis distal AD,Renal tubular acidosis distal AR,RENAL TUBULAR ACIDOSIS PROXIMAL WITH OCULAR ABNORMALITIES AND MENTAL RETARDATION,RENAL TUBULAR DYSGENESIS,Renal tubular dysgenesis of genetic origin,Renal tubulopathy-encephalopathy-liver failure syndrome,RENAL-COLOBOMA SYNDROME,Renal-Hepatic ciliopathy,RENAL-HEPATIC-PANCREATIC DYSPLASIA,RENAL-HEPATIC-PANCREATIC DYSPLASIA 1,RENAL-HEPATIC-PANCREATIC DYSPLASIA 2,Renin-angiotensin-aldosterone system-blocker-induced angioedema,RENPENNING SYNDROME 1,RERE-related neurodevelopmental syndrome,Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha,Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta,Resistance to thyrotropin-releasing hormone syndrome,Respiratory chain disorder,RESPIRATORY PAPILLOMATOSIS JUVENILE RECURRENT CONGENITAL,RESTING HEART RATE VARIATION IN,Restrictive dermopathy,RESTRICTIVE DERMOPATHY LETHAL,RETICULAR DYSGENESIS,Reticular dystrophy of the retinal pigment epithelium,Reticulate acropigmentation of Kitamura,RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS,Retinal arterial tortuosity,Retinal arteries tortuosity of,RETINAL CONE DYSTROPHY 3 PDE6H,RETINAL CONE DYSTROPHY 3A,RETINAL CONE DYSTROPHY 3B,RETINAL CONE DYSTROPHY 4,RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT,Retinal dystrophy and obesity,Retinal dystrophy iris coloboma and comedogenic acne syndrome,Retinal dystrophy juvenile cataracts and short stature syndrome,RETINAL DYSTROPHY OPTIC NERVE EDEMA SPLENOMEGALY ANHIDROSIS AND MIGRAINE HEADACHE SYNDROME,Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities,Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies,RETINAL DYSTROPHY WITH LEUKODYSTROPHY,RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES,RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA,Retinal macular dystrophy type 2,RETINAL NON-ATTACHMENT CONGENITAL NON-SYNDROMIC,Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations,Retinitis pigmentosa,RETINITIS PIGMENTOSA 1,RETINITIS PIGMENTOSA 10,RETINITIS PIGMENTOSA 11,RETINITIS PIGMENTOSA 12,RETINITIS PIGMENTOSA 13,RETINITIS PIGMENTOSA 14,RETINITIS PIGMENTOSA 18,RETINITIS PIGMENTOSA 19,RETINITIS PIGMENTOSA 2,RETINITIS PIGMENTOSA 20,RETINITIS PIGMENTOSA 23,RETINITIS PIGMENTOSA 25,RETINITIS PIGMENTOSA 26,RETINITIS PIGMENTOSA 27,Retinitis Pigmentosa 28,RETINITIS PIGMENTOSA 3,RETINITIS PIGMENTOSA 30,RETINITIS PIGMENTOSA 31,Retinitis pigmentosa 32,RETINITIS PIGMENTOSA 33,RETINITIS PIGMENTOSA 35,RETINITIS PIGMENTOSA 36,RETINITIS PIGMENTOSA 37,RETINITIS PIGMENTOSA 38,RETINITIS PIGMENTOSA 39,RETINITIS PIGMENTOSA 4,RETINITIS PIGMENTOSA 40,RETINITIS PIGMENTOSA 41,RETINITIS PIGMENTOSA 42,RETINITIS PIGMENTOSA 43,RETINITIS PIGMENTOSA 44,RETINITIS PIGMENTOSA 45,RETINITIS PIGMENTOSA 46,RETINITIS PIGMENTOSA 47,RETINITIS PIGMENTOSA 48,RETINITIS PIGMENTOSA 49,RETINITIS PIGMENTOSA 50,RETINITIS PIGMENTOSA 51,RETINITIS PIGMENTOSA 54,RETINITIS PIGMENTOSA 55,RETINITIS PIGMENTOSA 56,RETINITIS PIGMENTOSA 57,Retinitis pigmentosa 58,Retinitis pigmentosa 59,Retinitis pigmentosa 60,RETINITIS PIGMENTOSA 61,REtinitis pigmentosa 62,RETINITIS PIGMENTOSA 66,Retinitis pigmentosa 67,RETINITIS PIGMENTOSA 68,RETINITIS PIGMENTOSA 69,RETINITIS PIGMENTOSA 7,RETINITIS PIGMENTOSA 70,RETINITIS PIGMENTOSA 71,RETINITIS PIGMENTOSA 72,RETINITIS PIGMENTOSA 73,RETINITIS PIGMENTOSA 74,RETINITIS PIGMENTOSA 75,RETINITIS PIGMENTOSA 76,RETINITIS PIGMENTOSA 77,RETINITIS PIGMENTOSA 78,RETINITIS PIGMENTOSA 79,RETINITIS PIGMENTOSA 80,RETINITIS PIGMENTOSA 81,RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS,RETINITIS PIGMENTOSA 83,RETINITIS PIGMENTOSA 84,RETINITIS PIGMENTOSA 85,RETINITIS PIGMENTOSA 86,RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT,RETINITIS PIGMENTOSA 88,RETINITIS PIGMENTOSA 89,RETINITIS PIGMENTOSA 9,RETINITIS PIGMENTOSA 90,RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS,Retinitis pigmentosa skeletal anomalies and intellectual disability,RETINITIS PIGMENTOSA TYPE 51,RETINITIS PIGMENTOSA TYPE 55,RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES,RETINITIS PIGMENTOSA X-LINKED AND SINORESPIRATORY INFECTIONS WITH OR WITHOUT DEAFNESS,Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome,Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome,RETINITIS PUNCTATA ALBESCENS,RETINOBLASTOMA,RETINOPATHY OF PREMATURITY,RETINOSCHISIS 1 X-LINKED JUVENILE,Rett Syndrome,Rett syndrome congenital variant,RETT SYNDROME: RTT,Revesz syndrome,Reynolds syndrome,RFT1-CDG,RFVT2-related riboflavin transporter deficiency,RFVT3-related riboflavin transporter deficiency,Rh deficiency syndrome,RH-NULL AMORPH TYPE,RH-NULL REGULATOR TYPE,Rhabdoid predisposition syndrome 1,RHABDOID TUMOR PREDISPOSITION SYNDROME 1,Rhabdoid tumor predisposition syndrome 2,RHABDOMYOSARCOMA 2,RHABDOMYOSARCOMA EMBRYONAL 1,Rhabdomyosarcoma embryonal 2,Rheumatoid arthritis,RHEUMATOID ARTHRITIS SYSTEMIC JUVENILE,Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis,Rhizomelic chondrodysplasia punctata type 1,Rhizomelic chondrodysplasia punctata type 2,Rhizomelic chondrodysplasia punctata type 3,RHIZOMELIC CHONDRODYSPLASIA PUNCTATA TYPE 5,RHIZOMELIC LIMB SHORTENING WITH DYSMORPHIC FEATURES,RHYNS syndrome,RIBOFLAVIN DEFICIENCY,Riboflavin-Responsive and Non-responsive Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.,RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY,Ribose-5-P isomerase deficiency,Richieri Costa-Pereira syndrome,RICHIERI-COSTA-PEREIRA SYNDROME,rickets vitamin D-dependent type 2A,RIDDLE syndrome,RIEGER ANOMALY,RIGHT ATRIAL ISOMERISM,Right sided atrial isomerism,RIGID SPINE MUSCULAR DYSTROPHY 1,Rigid spine syndrome,RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME LETHAL NEONATAL,RIMS2 Syndromic Congenital Cone-Rod Synaptic Disease,RIN2 syndrome,RING DERMOID OF CORNEA,RIPPLING MUSCLE DISEASE,RIPPLING MUSCLE DISEASE 2,RITSCHER-SCHINZEL SYNDROME 1,Ritscher-schinzel syndrome 2,RITSCHER-SCHINZEL SYNDROME 3,RNF13-related severe early-onset epileptic encephalopathy,ROBERTS SYNDROME,Roberts-SC phocomelia syndrome,ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES,ROBINOW SYNDROME AUTOSOMAL DOMINANT 1,ROBINOW SYNDROME AUTOSOMAL DOMINANT 2,ROBINOW SYNDROME AUTOSOMAL DOMINANT 3,ROBINOW SYNDROME AUTOSOMAL RECESSIVE 1,ROBINOW SYNDROME AUTOSOMAL RECESSIVE 2,ROBINOW-SORAUF SYNDROME,ROIFMAN SYNDROME,Rolandic epilepsy,ROLANDIC EPILEPSY MENTAL RETARDATION AND SPEECH DYSPRAXIA X-LINKED,Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome,Rolandic epilepsy-speech dyspraxia syndrome,Romano-Ward syndrome,Rothmund-Thomson Syndrome Type 1,Rothmund-Thomson syndrome type 2,Rotor syndrome,ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA,Roussy-Levy syndrome,RPS19-Related Diamond-Blackfan Anemia,RUBINSTEIN-TAYBI SYNDROME 1,RUBINSTEIN-TAYBI SYNDROME 2,Rubinstein-Taybi syndrome due to 16p13.3 microdeletion,Rubinstein-Taybi syndrome due to CREBBP mutations,Rubinstein-Taybi syndrome due to EP300 haploinsufficiency,RUBINSTEIN-TAYBI SYNDROME TYPE 1,RUBINSTEIN-TAYBI SYNDROME TYPE 2,RUIJS-AALFS SYNDROME,S-adenosylhomocysteine hydrolase deficiency,Saccharopinuria,Sacral agenesis with vertebral anomalies,Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome,SACRAL DEFECT WITH ANTERIOR MENINGOCELE,SAETHRE-CHOTZEN SYNDROME,Saldino-Mainzer syndrome,SALIH MYOPATHY,SALIVARY GLAND ADENOMA PLEOMORPHIC,SALLA DISEASE,SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME,SANDESTIG-STEFANOVA SYNDROME,SANDHOFF DISEASE,Sandhoff disease adult form,Sandhoff disease infantile form,Sandhoff disease juvenile form,Sanfilippo syndrome type A,Sanfilippo syndrome type B,Sanfilippo syndrome type C,Sanfilippo syndrome type D,Sarcoidosis,SARCOIDOSIS SUSCEPTIBILITY TO 1,SARCOIDOSIS SUSCEPTIBILITY TO 2,SARCOMA SYNOVIAL,SARCOSINEMIA,SARS2-related hyperuricemia pulmonary hypertension renal failure and alkalosis,SATB1-related developmental disorder monoallelic,SATB2-associated syndrome due to a chromosomal rearrangement,SATB2-associated syndrome due to a pathogenic variant,SAUL-WILSON SYNDROME,SAY-BARBER-BIESECKER-YOUNG-SIMPSON SYNDROME,SCA14,SCAF4-related Neurodevelopmental Disorder,Scalp-ear-nipple syndrome,Scaphocephaly maxillary retrusion and mental retardation,SCAPULOPERONEAL MYOPATHY MYH7-RELATED,SCAPULOPERONEAL MYOPATHY X-LINKED DOMINANT,SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY,SCAPULOPERONEAL SYNDROME NEUROGENIC KAESER TYPE,SCHAAF-YANG SYNDROME,SCHEIE SYNDROME,Schilbach-Rott syndrome,Schimke immuno-osseous dysplasia,SCHIMKE IMMUNOOSSEOUS DYSPLASIA,SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME,SCHINDLER DISEASE TYPE I,Schinzel-Giedion midface retraction syndrome,Schinzel-Giedion syndrome,Schizencephaly,Schizophrenia,Schizophrenia 15,SCHIZOPHRENIA 18,SCHIZOPHRENIA 19,SCHIZOPHRENIA 4,SCHIZOPHRENIA 6,SCHIZOPHRENIA 9,SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA,SCHNECKENBECKEN DYSPLASIA,SCHNYDER CORNEAL DYSTROPHY,Schopf-Schulz-Passarge syndrome,Schuurs-hoeijmakers syndrome,Schwannomatosis,SCHWANNOMATOSIS 1,Schwannomatosis 2,Schwartz Jampel syndrome type 1,Schwartz-Jampel syndrome,SCLEROSING CHOLANGITIS NEONATAL,SCLEROSTEOSIS,SCLEROSTEOSIS 1,SCLEROSTEOSIS 2,SCN1A-Related Seizure Disorders,SCOTT SYNDROME,SCUBE3-related developmental disorder,SEA-BLUE HISTIOCYTE DISEASE,Sea-blue histiocytosis,Sebocystomatosis,Seborrhea-like dermatitis with psoriasiform elements,Seckel syndrome,SECKEL SYNDROME 1,SECKEL SYNDROME 10,SECKEL SYNDROME 2,SECKEL SYNDROME 4,SECKEL SYNDROME 5,SECKEL SYNDROME 6,SECKEL SYNDROME 7,Seckel syndrome 8,Seckel syndrome 9,SECKEL SYNDROME TYPE 1,SEDOHEPTULOKINASE DEFICIENCY,Segawa syndrome autosomal recessive,Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome,Segmental progressive overgrowth syndrome with fibroadipose hyperplasia,SEIZURES BENIGN FAMILIAL INFANTILE 2,SEIZURES BENIGN FAMILIAL INFANTILE 3,SEIZURES BENIGN FAMILIAL INFANTILE 5,SEIZURES BENIGN FAMILIAL NEONATAL 1,SEIZURES BENIGN FAMILIAL NEONATAL 2,Seizures cortical blindness and microcephaly syndrome,SEIZURES EARLY-ONSET WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS,SEIZURES SCOLIOSIS AND MACROCEPHALY/MICROCEPHALY SYNDROME,SEIZURES SENSORINEURAL DEAFNESS ATAXIA MENTAL RETARDATION AND ELECTROLYTE IMBALANCE,Seizures-scoliosis-macrocephaly syndrome,SEIZURES-SENSORINEURAL DEAFNESS-ATAXIA-MENTAL RETARDATION-ELECTROLYTE IMBALANCE,SELENON-related myopathy,Self-improving collodion baby,Self-improving dystrophic epidermolysis bullosa,SEMA3A-related skeletal dysplasia,Semantic dementia,Semilobar holoprosencephaly,Sengers syndrome,Senior-Boichis syndrome,Senior-Loken syndrome,SENIOR-LOKEN SYNDROME 1,SENIOR-LOKEN SYNDROME 4,SENIOR-LOKEN SYNDROME 5,SENIOR-LOKEN SYNDROME 6,SENIOR-LOKEN SYNDROME 7,SENIOR-LOKEN SYNDROME 8,Senior-Loken syndrome 9,Sensorineural deafness with dilated cardiomyopathy,Sensorineural Hearing Loss Hypoglycemia and Multiple OXPHOS Complex Deficiencies,SENSORY ATAXIC NEUROPATHY DYSARTHRIA AND OPHTHALMOPARESIS,Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome,Septo-optic dysplasia spectrum,SEPTOOPTIC DYSPLASIA,Septopreoptic holoprosencephaly,SERKAL SYNDROME,SERPIN PEPTIDASE INHIBITOR CLADE A MEMBER 2 PSEUDOGENE,Serrated polyposis syndrome,SESSILE SERRATED POLYPOSIS CANCER SYNDROME,SET syndrome,SETD1B associated intellectual disability epilepsy and autism,SETD2-associated Overgrowth Syndrome,SETLEIS SYNDROME,Severe achondroplasia-developmental delay-acanthosis nigricans syndrome,Severe Asphyxiating Thoracic Dysplasia,Severe autosomal dominant nocturnal frontal lobe epilepsy,Severe autosomal recessive macrothrombocytopenia,Severe Canavan disease,Severe Cobblestone Lissencephaly,Severe Combined Immune Deficiency Autosomal Recessive T Cell-Negative B Cell -Positive NK Cell-Negative JAK3-Related,SEVERE COMBINED IMMUNODEFICIENCY AUTOSOMAL RECESSIVE T CELL-NEGATIVE B CELL-NEGATIVE NK CELL-NEGATIVE DUE TO ADENOSINE DEAMINASE DEFICIENCY,SEVERE COMBINED IMMUNODEFICIENCY AUTOSOMAL RECESSIVE T CELL-NEGATIVE B CELL-NEGATIVE NK CELL-POSITIVE,Severe combined immunodeficiency autosomal recessive T cell-negative B cell-positive NK cell-negative,Severe combined immunodeficiency autosomal recessive T cell-negative B cell-positive NK cell-positive,Severe combined immunodeficiency due to adenosine deaminase deficiency,Severe combined immunodeficiency due to CARD11 deficiency,Severe combined immunodeficiency due to CARMIL2 deficiency,Severe combined immunodeficiency due to complete RAG1/2 deficiency,Severe combined immunodeficiency due to CORO1A deficiency,Severe combined immunodeficiency due to CTPS1 deficiency,Severe combined immunodeficiency due to DCLRE1C deficiency,Severe combined immunodeficiency due to DNA-PKcs deficiency,Severe combined immunodeficiency due to FOXN1 deficiency,Severe combined immunodeficiency due to IKK2 deficiency,Severe combined immunodeficiency due to LAT deficiency,Severe combined immunodeficiency due to LCK deficiency,SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY GROWTH RETARDATION AND SENSITIVITY TO IONIZING RADIATION,SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION,SEVERE COMBINED IMMUNODEFICIENCY X-LINKED,Severe congenital hypochromic anemia with ringed sideroblasts,Severe congenital nemaline myopathy,Severe congenital neutropenia,SEVERE CUTANEOUS ADVERSE REACTION SUSCEPTIBILITY TO TOXIC EPIDERMAL NECROLYSIS SUSCEPTIBILITY TO INCLUDED,severe dermatitis multiple allergies and metabolic wasting,Severe dermatitis-multiple allergies-metabolic wasting syndrome,Severe early-childhood-onset retinal dystrophy,Severe early-onset axonal neuropathy due to MFN2 deficiency,Severe early-onset encephalopathy with progressive microcephaly,SEVERE EARLY-ONSET EPILEPSY,Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number,Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency,Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency,Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers,Severe generalized junctional epidermolysis bullosa,Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome,Severe Growth Retardation Spine Malformations and Developmental Delays,Severe hemophilia A,Severe hemophilia B,Severe hereditary thrombophilia due to congenital protein C deficiency,Severe hereditary thrombophilia due to congenital protein S deficiency,Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome,Severe ID with neuronal migration disorder,Severe Infantile Syndromic Encephalopathy,Severe Infantile-Onset Encephalopathy,Severe intellectual disability and progressive spastic paraplegia,Severe intellectual disability epilepsy and cataracts,Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome,Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome,Severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome,Severe intellectual disability-progressive spastic diplegia syndrome,Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome,Severe microcephaly and short stature,Severe microcephaly short stature and intellectual disability,Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome,Severe myopia-generalized joint laxity-short stature syndrome,Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion,Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency,Severe Neonatal- Childhood- or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies,Severe neonatal-onset encephalopathy with microcephaly,Severe neurodegenerative syndrome with lipodystrophy,Severe Neurodevelopmental Disability Hypotonia and Seizures,Severe Neurodevelopmental Disease with Seizures,Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract,Severe Neurodevelopmental Syndrome,Severe obesity with neurobehavioral features,Severe phosphoribosylpyrophosphate synthetase superactivity,Severe primary trimethylaminuria,Severe pseudo-TORCH syndrome,Severe syndromic form of thoracic aortic aneurysm and dissection,Severe X-linked mitochondrial encephalomyopathy,SEX REVERSAL TYPE 3,Sezary syndrome,SHAHEEN SYNDROME,SHASHI-PENA SYNDROME,Sheldon-Hall syndrome,SHMT2-related neurodevelopmental syndrome,Short chain acyl-CoA dehydrogenase deficiency,SHORT QT SYNDROME 1,SHORT QT SYNDROME 2,SHORT QT SYNDROME 3,Short rib-polydactyly syndorme type II,Short rib-polydactyly syndrome Beemer-Langer type,Short rib-polydactyly syndrome Majewski type,Short rib-polydactyly syndrome Saldino-Noonan type,Short rib-polydactyly syndrome type 5,Short rib-polydactyly syndrome Verma-Naumoff type,SHORT SLEEP FAMILIAL NATURAL 1,SHORT SLEEP FAMILIAL NATURAL 2,SHORT STATURE AMELOGENESIS IMPERFECTA AND SKELETAL DYSPLASIA WITH SCOLIOSIS,SHORT STATURE AND ADVANCED BONE AGE WITH OR WITHOUT EARLY-ONSETOSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS,SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES,SHORT STATURE AUDITORY CANAL ATRESIA MANDIBULAR HYPOPLASIA AND SKELETAL ABNORMALITIES,SHORT STATURE BRACHYDACTYLY IMPAIRED INTELLECTUAL DEVELOPMENT AND SEIZURES,Short Stature Developmental Delay and Congenital Heart Defects,Short stature due to GHSR deficiency,Short stature due to growth hormone qualitative anomaly,Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia,Short stature due to partial GHR deficiency,Short stature due to primary acid-labile subunit deficiency,SHORT STATURE FACIAL DYSMORPHISM AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 1,SHORT STATURE FACIAL DYSMORPHISM AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 2,SHORT STATURE HEARING LOSS RETINITIS PIGMENTOSA AND DISTINCTIVE FACIES,Short stature idiopathic X-linked,SHORT STATURE MICROCEPHALY AND ENDOCRINE DYSFUNCTION,SHORT STATURE OLIGODONTIA DYSMORPHIC FACIES AND MOTOR DELAY,Short stature onychodysplasia facial dysmorphism and hypotrichosis,SHORT STATURE OPTIC NERVE ATROPHY AND PELGER-HUET ANOMALY,Short stature palatal anomalies congenital heart disease and skeletal malformations,SHORT STATURE RHIZOMELIC WITH MICROCEPHALY MICROGNATHIA AND DEVELOPMENTAL DELAY,SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES,SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES,Short stature-advanced bone age-early onset osteoarthritis syndrome,Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome,Short stature-brachydactyly-obesity-global developmental delay syndrome,Short stature-delayed bone age due to thyroid hormone metabolism deficiency,Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome,Short stature-optic atrophy-Pelger-Huet anomaly syndrome,Short stature-pituitary and cerebellar defects-small sella turcica syndrome,SHORT syndrome,Short-Rib Polydactyly,SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 2 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY,Short-rib thoracic dysplasia 3 with or without polydactyly,Short-rib thoracic dysplasia 4 with or without polydactyly,SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY,SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY,Shox-related short stature,Shprintzen-Goldberg craniosynostosis syndrome,SHPRINTZEN-GOLDBERG SYNDROME,SHUKLA-VERNON SYNDROME,SHWACHMAN-DIAMOND SYNDROME,SHWACHMAN-DIAMOND SYNDROME 1,SHWACHMAN-DIAMOND SYNDROME 2,SIAH1-associated neurodevelopmental disorder,Sialidosis,Sialidosis type 1,SIALURIA,Sick sinus syndrome 1,SICK SINUS SYNDROME 2,SICK SINUS SYNDROME 3 SUSCEPTIBILITY TO,SICKLE CELL ANEMIA,Sickle cell-beta-thalassemia disease syndrome,Sickle cell-hemoglobin C disease syndrome,Sickle cell-hemoglobin D disease syndrome,Sickle cell-hemoglobin E disease syndrome,SIDDIQI SYNDROME,SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME,SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY PERIODIC FEVERS AND DEVELOPMENTAL DELAY,SIFRIM-HITZ-WEISS SYNDROME,Silent pituitary adenoma,SILVER-RUSSELL SYNDROME 1,SILVER-RUSSELL SYNDROME 3,SILVER-RUSSELL SYNDROME 4,Silver-Russell syndrome 5,Silver-Russell syndrome due to 11p15 microduplication,Silver-Russell syndrome due to a point mutation,Silver-Russell syndrome due to an imprinting defect of 11p15,SIM1-related Prader-Willi-like syndrome,Simpson-Golabi-Behmel syndrome,SIMPSON-GOLABI-BEHMEL SYNDROME TYPE 1,Simpson-Golabi-Behmel syndrome type 2,SIN3A-related intellectual disability syndrome due to a point mutation,Singleton-Merten dysplasia,Singleton-Merten syndrome,SINGLETON-MERTEN SYNDROME 1,SINGLETON-MERTEN SYNDROME 2,Sinoatrial node dysfunction and deafness,Sinus Bradycardia and Cognitive Disability,SITOSTEROLEMIA,SITOSTEROLEMIA 1,SITOSTEROLEMIA 2,Situs ambiguus,Situs inversus totalis,SIX2-related frontonasal dysplasia,SJOEGREN-LARSSON SYNDROME,Sjogren-Larsson syndrome,SKELETAL DEFECTS GENITAL HYPOPLASIA AND MENTAL RETARDATION,SKELETAL DYSPLASIA MILD WITH JOINT LAXITY AND ADVANCED BONE AGE,Skeletal dysplasia with severe neurological disease,Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome,Skeletal Ewing sarcoma,SKELETAL MUSCLE GLYCOGEN CONTENT AND METABOLISM QUANTITATIVE TRAIT LOCUS,Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome,SKIN CREASES CONGENITAL SYMMETRIC CIRCUMFERENTIAL 1,Skin creases congenital symmetric circumferential 2,SKIN FRAGILITY-WOOLLY HAIR SYNDROME,Skin fragility-woolly hair-palmoplantar keratoderma syndrome,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 1,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 10,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 11,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 2,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 3,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 5,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 6,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 7,Skin/hair/eye pigmentation variation in 8,SKIN/HAIR/EYE PIGMENTATION VARIATION IN 9,SKRABAN-DEARDORFF SYNDROME,SLC12A5-related epilepsy of infancy with migrating focal seizures,SLC25A1-related Neurometabolic Disorder,SLC35A1-CDG,SLC35A2-CDG,SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome,SLC39A8-CDG,SLC5A6-related Neurodevelopmental Disorder,SLIT-ROBO RHO GTPASE-ACTIVATING PROTEIN 3,SLOWED NERVE CONDUCTION VELOCITY AUTOSOMAL DOMINANT,SMAD3-Related Loeys-Dietz Syndrome,Small cell cancer of the lung,Small cell carcinoma of the ovary,Small cell lung cancer,SMALL PATELLA SYNDROME,SMARCA4-deficient sarcoma of thorax,SMC1A-related Epileptic Encephalopathy,SMG8-related Developmental Disorder,SMG9 Multiple Congenital Anomaly Syndrome,SMITH-KINGSMORE SYNDROME,SMITH-LEMLI-OPITZ SYNDROME,SMITH-MAGENIS SYNDROME,SMITH-MCCORT DYSPLASIA,SMITH-MCCORT DYSPLASIA 1,SMITH-MCCORT DYSPLASIA 2,SMO-related developmental disorder,SMOKING AS A QUANTITATIVE TRAIT LOCUS 3,Smoldering systemic mastocytosis,SNEDDON SYNDROME,SNIJDERS BLOK-CAMPEAU SYNDROME,SNIJDERS BLOK-FISHER SYNDROME,SNOWFLAKE VITREORETINAL DEGENERATION,SNYDER-ROBINSON SYNDROME,Sodium channelopathy-related small fiber neuropathy,SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1,Solitary fibrous tumor/hemangiopericytoma,SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR,SOLUBLE INTERLEUKIN-6 RECEPTOR SERUM LEVEL OF QUANTITATIVE TRAIT LOCUS,SOLUTE CARRIER FAMILY 4 ANION EXCHANGER MEMBER 1,SORBITOL DEHYDROGENASE DEFICIENCY WITH PERIPHERAL NEUROPATHY,SORSBY FUNDUS DYSTROPHY,Sorsby pseudoinflammatory fundus dystrophy,SOTOS SYNDROME,SOTOS SYNDROME 1,SOTOS SYNDROME 2,SOTOS SYNDROME 3,Southeast Asian ovalocytosis,SOX6-related neurodevelopmental syndrome,SPAST-related developmental disorder monoallelic,SPASTIC ATAXIA 1 AUTOSOMAL DOMINANT,SPASTIC ATAXIA 2 AUTOSOMAL RECESSIVE,SPASTIC ATAXIA 3 AUTOSOMAL RECESSIVE,SPASTIC ATAXIA 4 AUTOSOMAL RECESSIVE,SPASTIC ATAXIA 5 AUTOSOMAL RECESSIVE,SPASTIC ATAXIA 8 AUTOSOMAL RECESSIVE WITH HYPOMYELINATING LEUKODYSTROPHY,SPASTIC ATAXIA 9 AUTOSOMAL RECESSIVE,SPASTIC ATAXIA CHARLEVOIX-SAGUENAY TYPE,Spastic ataxia-dysarthria due to glutaminase deficiency,SPASTIC PARALYSIS INFANTILE-ONSET ASCENDING,SPASTIC PARAPLEGIA 10 AUTOSOMAL DOMINANT,Spastic paraplegia 11 autosomal recessive,SPASTIC PARAPLEGIA 12 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 13 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 15 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 17 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 18 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 2 X-LINKED,SPASTIC PARAPLEGIA 20 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 23 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 26 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 28 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 3 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 30 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 31 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 33 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 35 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 39 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 4 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 42 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 43 AUTOSOMAL RECESSIVE,Spastic paraplegia 44,SPASTIC PARAPLEGIA 44 AUTOSOMAL RECESSIVE,Spastic paraplegia 45 autosomal recessive,SPASTIC PARAPLEGIA 46 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 47 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 48 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 49 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 50 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 51 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 52 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 53 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 54 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 55 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 56 AUTOSOMAL RECESSIVE,Spastic paraplegia 57 autosomal recessive,SPASTIC PARAPLEGIA 5A AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 6 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 61 AUTOSOMAL RECESSIVE,Spastic paraplegia 62 autosomal recessive,Spastic paraplegia 63 autosomal recessive,Spastic paraplegia 64 autosomal recessive,SPASTIC PARAPLEGIA 7 AUTOSOMAL RECESSIVE,Spastic paraplegia 72 autosomal recessive,SPASTIC PARAPLEGIA 73 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 74 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 75 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 76 AUTOSOMAL RECESSIVE,Spastic paraplegia 77 autosomal recessive,SPASTIC PARAPLEGIA 78 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 79 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 8 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 80 AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 81 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 82 AUTOSOMAL RECESSIVE,SPASTIC PARAPLEGIA 83 AUTOSOMAL RECESSIVE,Spastic paraplegia 9 autosomal dominant,SPASTIC PARAPLEGIA 9A AUTOSOMAL DOMINANT,SPASTIC PARAPLEGIA 9B AUTOSOMAL RECESSIVE,Spastic paraplegia and psychomotor retardation with or without seizures,SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15,SPASTIC PARAPLEGIA INTELLECTUAL DISABILITY NYSTAGMUS AND OBESITY,SPASTIC PARAPLEGIA OPTIC ATROPHY AND NEUROPATHY,Spastic paraplegia type 2,Spastic paraplegia type 7,SPASTIC PARAPLEGIA X-LINKED TYPE 2,Spastic paraplegia-11,Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome,Spastic paraplegia-optic atrophy-neuropathy syndrome,Spastic paraplegia-Paget disease of bone syndrome,Spastic paraplegia-severe developmental delay-epilepsy syndrome,SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA PROGRESSIVE,SPASTIC TETRAPLEGIA THIN CORPUS CALLOSUM AND PROGRESSIVE MICROCEPHALY,Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome,Spasticity childhood-onset with hyperglycinemia,SPECC1L-related hypertelorism syndrome,SPECIFIC GRANULE DEFICIENCY 1,SPECIFIC GRANULE DEFICIENCY 2,SPECIFIC LANGUAGE IMPAIRMENT 5,Spectrin-associated autosomal recessive cerebellar ataxia,SPEECH-LANGUAGE DISORDER 1,SPEN-related developmental disorder monoallelic,SPERMATOGENIC FAILURE 1,SPERMATOGENIC FAILURE 10,SPERMATOGENIC FAILURE 11,SPERMATOGENIC FAILURE 12,Spermatogenic failure 13,Spermatogenic failure 14,Spermatogenic failure 15,SPERMATOGENIC FAILURE 16,SPERMATOGENIC FAILURE 17,SPERMATOGENIC FAILURE 18,SPERMATOGENIC FAILURE 19,SPERMATOGENIC FAILURE 20,SPERMATOGENIC FAILURE 21,SPERMATOGENIC FAILURE 22,SPERMATOGENIC FAILURE 23,SPERMATOGENIC FAILURE 24,SPERMATOGENIC FAILURE 25,SPERMATOGENIC FAILURE 26,SPERMATOGENIC FAILURE 27,SPERMATOGENIC FAILURE 28,SPERMATOGENIC FAILURE 29,Spermatogenic failure 3,SPERMATOGENIC FAILURE 30,SPERMATOGENIC FAILURE 31,SPERMATOGENIC FAILURE 32,SPERMATOGENIC FAILURE 33,SPERMATOGENIC FAILURE 34,SPERMATOGENIC FAILURE 35,SPERMATOGENIC FAILURE 36,SPERMATOGENIC FAILURE 37,SPERMATOGENIC FAILURE 38,SPERMATOGENIC FAILURE 39,SPERMATOGENIC FAILURE 4,SPERMATOGENIC FAILURE 40,SPERMATOGENIC FAILURE 41,SPERMATOGENIC FAILURE 42,SPERMATOGENIC FAILURE 43,SPERMATOGENIC FAILURE 44,SPERMATOGENIC FAILURE 45,SPERMATOGENIC FAILURE 46,SPERMATOGENIC FAILURE 47,SPERMATOGENIC FAILURE 48,SPERMATOGENIC FAILURE 49,SPERMATOGENIC FAILURE 5,SPERMATOGENIC FAILURE 50,SPERMATOGENIC FAILURE 51,SPERMATOGENIC FAILURE 52,SPERMATOGENIC FAILURE 6,SPERMATOGENIC FAILURE 7,Spermatogenic failure 8,SPERMATOGENIC FAILURE 9,SPERMATOGENIC FAILURE X-LINKED 2,SPERMATOGENIC FAILURE X-LINKED 3,SPERMATOGENIC FAILURE Y-LINKED 2,SPHEROCYTOSIS TYPE 1,SPHEROCYTOSIS TYPE 2,SPHEROCYTOSIS TYPE 3,SPHEROCYTOSIS TYPE 4,SPHEROCYTOSIS TYPE 5,Spheroid body myopathy,Spinal and Bulbar Muscular Atrophy,SPINAL AND BULBAR MUSCULAR ATROPHY X-LINKED 1,Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy,SPINAL MUSCULAR ATROPHY DISTAL AUTOSOMAL RECESSIVE 1,SPINAL MUSCULAR ATROPHY DISTAL AUTOSOMAL RECESSIVE 2,SPINAL MUSCULAR ATROPHY DISTAL AUTOSOMAL RECESSIVE 4,SPINAL MUSCULAR ATROPHY DISTAL AUTOSOMAL RECESSIVE 5,Spinal muscular atrophy distal X-linked 3,SPINAL MUSCULAR ATROPHY INFANTILE JAMES TYPE,Spinal muscular atrophy jokela type,SPINAL MUSCULAR ATROPHY LATE-ONSET FINKEL TYPE,SPINAL MUSCULAR ATROPHY LOWER EXTREMITY-PREDOMINANT 1 AUTOSOMALDOMINANT,SPINAL MUSCULAR ATROPHY LOWER EXTREMITY-PREDOMINANT 2A CHILDHOOD ONSET AUTOSOMAL DOMINANT,SPINAL MUSCULAR ATROPHY LOWER EXTREMITY-PREDOMINANT 2B PRENATAL ONSET AUTOSOMAL DOMINANT,Spinal muscular atrophy lower extremity-predominant AD,SPINAL MUSCULAR ATROPHY TYPE I,SPINAL MUSCULAR ATROPHY TYPE II,SPINAL MUSCULAR ATROPHY TYPE III,SPINAL MUSCULAR ATROPHY TYPE IV,SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1,Spinal muscular atrophy with congenital bone fractures 2,SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY,Spinal Muscular Atrophy with Respiratory Distress 1,Spinal muscular atrophy with respiratory distress type 1,Spinal muscular atrophy with respiratory distress type 2,SPINAL MUSCULAR ATROPHY X-LINKED 2,Spinal muscular atrophy-progressive myoclonic epilepsy syndrome,SPINOCEREBELLAR ATAXIA 1,SPINOCEREBELLAR ATAXIA 10,SPINOCEREBELLAR ATAXIA 11,SPINOCEREBELLAR ATAXIA 12,SPINOCEREBELLAR ATAXIA 13,SPINOCEREBELLAR ATAXIA 14,SPINOCEREBELLAR ATAXIA 15,SPINOCEREBELLAR ATAXIA 17,Spinocerebellar ataxia 19,SPINOCEREBELLAR ATAXIA 2,SPINOCEREBELLAR ATAXIA 21,Spinocerebellar ataxia 23,SPINOCEREBELLAR ATAXIA 26,SPINOCEREBELLAR ATAXIA 27,SPINOCEREBELLAR ATAXIA 28,SPINOCEREBELLAR ATAXIA 29,Spinocerebellar ataxia 29 congenital nonprogressive,SPINOCEREBELLAR ATAXIA 31,SPINOCEREBELLAR ATAXIA 34,SPINOCEREBELLAR ATAXIA 35,SPINOCEREBELLAR ATAXIA 36,SPINOCEREBELLAR ATAXIA 37,Spinocerebellar ataxia 38,SPINOCEREBELLAR ATAXIA 40,Spinocerebellar ataxia 41,Spinocerebellar ataxia 42,SPINOCEREBELLAR ATAXIA 42 EARLY-ONSET SEVERE WITH NEURODEVELOPMENTAL DEFICITS,Spinocerebellar ataxia 43,SPINOCEREBELLAR ATAXIA 44,SPINOCEREBELLAR ATAXIA 45,SPINOCEREBELLAR ATAXIA 46,SPINOCEREBELLAR ATAXIA 47,SPINOCEREBELLAR ATAXIA 48,SPINOCEREBELLAR ATAXIA 5,SPINOCEREBELLAR ATAXIA 6,SPINOCEREBELLAR ATAXIA 7,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 10,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 11,Spinocerebellar ataxia autosomal recessive 12,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 13,Spinocerebellar ataxia autosomal recessive 14,Spinocerebellar ataxia autosomal recessive 15,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 16,Spinocerebellar ataxia autosomal recessive 17,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 18,Spinocerebellar ataxia autosomal recessive 2,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 20,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 21,Spinocerebellar ataxia autosomal recessive 22,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 23,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 24,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 25,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 26,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 27,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 28,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 4,Spinocerebellar ataxia autosomal recessive 7,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 8,Spinocerebellar ataxia autosomal recessive with axonal neuropathy 1,Spinocerebellar ataxia autosomal recessive with axonal neuropathy 2,SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE WITH AXONAL NEUROPATHY 3,Spinocerebellar ataxia type 1,Spinocerebellar ataxia type 10,Spinocerebellar ataxia type 11,Spinocerebellar ataxia type 12,Spinocerebellar ataxia type 13,Spinocerebellar ataxia type 14,Spinocerebellar ataxia type 15/16,Spinocerebellar ataxia type 17,Spinocerebellar ataxia type 18,Spinocerebellar ataxia type 19/22,Spinocerebellar ataxia type 2,Spinocerebellar ataxia type 21,Spinocerebellar ataxia type 23,Spinocerebellar ataxia type 26,Spinocerebellar ataxia type 27,Spinocerebellar ataxia type 28,Spinocerebellar ataxia type 29,Spinocerebellar ataxia type 31,Spinocerebellar ataxia type 34,Spinocerebellar ataxia type 35,Spinocerebellar ataxia type 36,Spinocerebellar ataxia type 37,Spinocerebellar ataxia type 38,Spinocerebellar ataxia type 4,Spinocerebellar ataxia type 40,Spinocerebellar ataxia type 41,Spinocerebellar ataxia type 42,Spinocerebellar ataxia type 43,Spinocerebellar ataxia type 5,Spinocerebellar ataxia type 6,Spinocerebellar ataxia type 7,Spinocerebellar ataxia type 8,Spinocerebellar ataxia with axonal neuropathy type 1,Spinocerebellar ataxia with axonal neuropathy type 2,SPINOCEREBELLAR ATAXIA WITH EPILEPSY,SPINOCEREBELLAR ATAXIA X-LINKED 1,SPLIT HAND AND FOOT MALFORMATION,Split hand-split foot-deafness syndrome,SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY,Split-foot malformation-mesoaxial polydactyly syndrome,Split-hand/foot malformation 1,SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS AUTOSOMALRECESSIVE,SPLIT-HAND/FOOT MALFORMATION 4,SPLIT-HAND/FOOT MALFORMATION 6,SPLIT-HAND/FOOT MALFORMATION TYPE 3,SPLIT-HAND/FOOT MALFORMATION TYPE 6,SPONASTRIME dysplasia,SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA,Spondylo-ocular syndrome,SPONDYLOARTHROPATHY SUSCEPTIBILITY TO 1,Spondylocarpotarsal synostosis,SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME,SPONDYLOCOSTAL DYSOSTOSIS 1 AUTOSOMAL RECESSIVE,SPONDYLOCOSTAL DYSOSTOSIS 2 AUTOSOMAL RECESSIVE,SPONDYLOCOSTAL DYSOSTOSIS 3 AUTOSOMAL RECESSIVE,SPONDYLOCOSTAL DYSOSTOSIS 4 AUTOSOMAL RECESSIVE,Spondylocostal dysostosis 5,Spondylocostal dysostosis 6 autosomal recessive,SPONDYLOCOSTAL DYSOSTOSIS TYPE 1,SPONDYLOCOSTAL DYSOSTOSIS TYPE 2,SPONDYLOCOSTAL DYSOSTOSIS TYPE 3,Spondyloenchondrodysplasia,Spondyloenchondrodysplasia with immune dysregulation,SPONDYLOEPIMETAPHYSEAL DYSPLASIA AGGRECAN TYPE,SPONDYLOEPIMETAPHYSEAL DYSPLASIA BOROCHOWITZ-CORMIER-DAIRE TYPE,Spondyloepimetaphyseal dysplasia congenita Strudwick type,SPONDYLOEPIMETAPHYSEAL DYSPLASIA DI ROCCO TYPE,Spondyloepimetaphyseal dysplasia Faden-Alkuraya type,Spondyloepimetaphyseal dysplasia Genevieve type,SPONDYLOEPIMETAPHYSEAL DYSPLASIA ISIDOR-TOUTAIN TYPE,SPONDYLOEPIMETAPHYSEAL DYSPLASIA KRAKOW TYPE,Spondyloepimetaphyseal dysplasia matrilin-3 type,SPONDYLOEPIMETAPHYSEAL DYSPLASIA MISSOURI TYPE,SPONDYLOEPIMETAPHYSEAL DYSPLASIA PAKISTANI TYPE,Spondyloepimetaphyseal dysplasia PAPSS2 type,SPONDYLOEPIMETAPHYSEAL DYSPLASIA SHOHAT TYPE,SPONDYLOEPIMETAPHYSEAL DYSPLASIA SHORT LIMB-HAND TYPE,SPONDYLOEPIMETAPHYSEAL DYSPLASIA SPONASTRIME TYPE,Spondyloepimetaphyseal dysplasia Strudwick type,SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION,Spondyloepimetaphyseal dysplasia with joint laxity,SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY TYPE 1,SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY TYPE 1 WITH OR WITHOUT FRACTURES,SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY TYPE 2,SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY TYPE 3,Spondyloepimetaphyseal dysplasia with multiple dislocations,Spondyloepimetaphyseal Dysplasia with Severe Short Stature,SPONDYLOEPIMETAPHYSEAL DYSPLASIA X-LINKED,Spondyloepimetaphyseal dysplasia X-linked with hypomyelinating leukodystrophy,Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome,SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA,Spondyloepiphyseal dysplasia Kimberley type,SPONDYLOEPIPHYSEAL DYSPLASIA KONDO-FU TYPE,Spondyloepiphyseal dysplasia Maroteaux type,Spondyloepiphyseal dysplasia Nishimura type,Spondyloepiphyseal dysplasia stanescu type,SPONDYLOEPIPHYSEAL DYSPLASIA TARDA,SPONDYLOEPIPHYSEAL DYSPLASIA TARDA X-LINKED,SPONDYLOEPIPHYSEAL DYSPLASIA TYPE KIMBERLEY,SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS,Spondyloepiphyseal dysplasia with metatarsal shortening,SPONDYLOMETAEPIPHYSEAL DYSPLASIA SHORT LIMB-HAND TYPE,Spondylometaphyseal dysplasia 'corner fracture' type,Spondylometaphyseal dysplasia axial,SPONDYLOMETAPHYSEAL DYSPLASIA KOZLOWSKI TYPE,SPONDYLOMETAPHYSEAL DYSPLASIA MEGARBANE-DAGHER-MELKI TYPE,Spondylometaphyseal dysplasia Schmidt type,Spondylometaphyseal dysplasia Sedaghatian type,Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy,SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY,Spondylometaphyseal Dysplasia with Corner Fractures,Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome,SPONDYLOOCULAR SYNDROME,SPONDYLOPERIPHERAL DYSPLASIA,Spondyloperipheral dysplasia-short ulna syndrome,SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES,SPOP-related Neurodevelopmental Disorder dominant negative,SPOP-related Neurodevelopmental Disorder gain of function,Sporadic fatal insomnia,Sporadic pheochromocytoma/secreting paraganglioma,Sporadic porphyria cutanea tarda,SPTBN1-related developmental disorder monoallelic,SQUALENE SYNTHASE DEFICIENCY,SQUAMOUS CELL CARCINOMA HEAD AND NECK,Squamous cell carcinoma of salivary glands,Squamous cell carcinoma of the esophagus,Squamous cell carcinoma of the hypopharynx,Squamous cell carcinoma of the larynx,Squamous cell carcinoma of the lip,Squamous cell carcinoma of the nasal cavity and paranasal sinuses,Squamous cell carcinoma of the oral cavity,Squamous cell carcinoma of the oropharynx,SRD5A3-CDG,SRRM2-related developmental disorder monoallelic,SRSF1-related developmental disorder monoallelic,SSR4-CDG,STAG1 syndromic intellectual disability,STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome,STAG2-related developmental delay with microcephaly and congenital anomalies,STANKIEWICZ-ISIDOR SYNDROME,Stapes ankylosis with broad thumbs and toes,STAR syndrome,STARGARDT DISEASE,STARGARDT DISEASE 1,STARGARDT DISEASE 3,STARGARDT DISEASE 4,STAT3-related early-onset multisystem autoimmune disease,STEATOCYSTOMA MULTIPLEX,Steel syndrome,Steinert myotonic dystrophy,Sterile multifocal osteomyelitis with periostitis and pustulosis,Stevens-Johnson syndrome,Stickler syndrome,Stickler syndrome type 1,STICKLER SYNDROME TYPE 1 NON-SYNDROMIC OCULAR,Stickler syndrome type 2,STICKLER SYNDROME TYPE 3,STICKLER SYNDROME TYPE 4,STICKLER SYNDROME TYPE I,STICKLER SYNDROME TYPE I NONSYNDROMIC OCULAR,STICKLER SYNDROME TYPE II,STICKLER SYNDROME TYPE IV,Stickler syndrome type V,Stiff skin syndrome,Sting-associated vasculopathy infantile-onset,STING-associated vasculopathy with onset in infancy,STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME,STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS,Stormorken syndrome,Stormorken-Sjaastad-Langslet syndrome,STRIATAL DEGENERATION AUTOSOMAL DOMINANT 1,Striatal degeneration autosomal dominant 2,Striate palmoplantar keratoderma,STRIATONIGRAL DEGENERATION CHILDHOOD-ONSET,STRIATONIGRAL DEGENERATION INFANTILE,STROKE ISCHEMIC,STROMME SYNDROME,STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS,STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME,STT3A-CDG,STT3B-CDG,Sturge-Weber syndrome,Stuttering familial persistent 1,Stuve-Wiedemann syndrome,Subcortical band heterotopia,SUBCORTICAL BAND HETEROTOPIA X-LINKED,SUBCUTANEOUS LIPODYSTROPHY DEAFNESS MANDIBULAR HYPOPLASIA AND MALE HYPOGONADISM,Subcutaneous panniculitis-like T-cell lymphoma,Submucosal cleft palate,Succinate-semialdehyde dehydrogenase deficiency,SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY,succinyl-CoA-3-ketoacid-CoA transferase deficiency,SUCCINYL-CoA:3-OXOACID CoA TRANSFERASE DEFICIENCY,SUCRASE-ISOMALTASE DEFICIENCY CONGENITAL,Sudden arrhythmic cardiac death after infectious or alcohol trigger,SUDDEN CARDIAC FAILURE ALCOHOL-INDUCED,SUDDEN CARDIAC FAILURE INFANTILE,SUDDEN INFANT DEATH SYNDROME,SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME,Sudden infant death-dysgenesis of the testes syndrome,SULEIMAN-EL-HATTAB SYNDROME,Sulfatidosis Juvenile Austin Type,SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY,Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A,Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B,Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C,SULFITE OXIDASE DEFICIENCY ISOLATED,Superficial epidermolytic ichthyosis,SUPRANUCLEAR PALSY PROGRESSIVE 1,SUPRAVALVULAR AORTIC STENOSIS,SUPT16H-related neurodevelopmental disorder,SURF1-related Charcot-Marie-Tooth disease type 4,SURFACTANT METABOLISM DYSFUNCTION PULMONARY 1,SURFACTANT METABOLISM DYSFUNCTION PULMONARY 2,SURFACTANT METABOLISM DYSFUNCTION PULMONARY 3,SURFACTANT METABOLISM DYSFUNCTION PULMONARY 4,SURFACTANT METABOLISM DYSFUNCTION PULMONARY 5,SUSCEPTIBILITY TO AUTISM TYPE 16,SUSCEPTIBILITY TO AUTISM TYPE 17,SUSCEPTIBILITY TO AUTISM X-LINKED TYPE 2,Susceptibility to infection due to TYK2 deficiency,Susceptibility to localized juvenile periodontitis,Susceptibility to respiratory infections associated with CD8alpha chain mutation,Susceptibility to viral and mycobacterial infections due to STAT1 deficiency,Sveinsson chorioretinal atrophy,SWEENEY-COX SYNDROME,Sweet syndrome,SYMPHALANGISM PROXIMAL 1A,SYMPHALANGISM PROXIMAL 1B,SYMPTOMATIC EPILEPSY AND SKULL DYSPLASIA,Symptomatic form of Coffin-Lowry syndrome in female carriers,Symptomatic form of fragile X syndrome in female carrier,Symptomatic form of hemochromatosis type 1,Symptomatic form of hemophilia A in female carriers,Symptomatic form of hemophilia B in female carriers,Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers,Synaptic congenital myasthenic syndromes,SYNCRIP-related developmental disorder monoallelic,SYNDACTYLY MESOAXIAL SYNOSTOTIC WITH PHALANGEAL REDUCTION,Syndactyly type 3,Syndactyly type 4,Syndactyly type 5,Syndactyly type 8,SYNDACTYLY TYPE III,SYNDACTYLY TYPE IV,SYNDACTYLY TYPE V,Syndactyly-telecanthus-anogenital and renal malformations syndrome,Syndromic congenital heart defects,Syndromic congenital sodium diarrhea,Syndromic diarrhea,Syndromic ID with severe microcephaly,Syndromic intellectual disability,Syndromic Intellectual Disability and Developmental Delay,Syndromic Intellectual Disability Resembling Other PP2A Related Neurodevelopmental Disorders,Syndromic INTELLECTUAL DISABILITY with or without congenital heart disease,Syndromic microphthalmia type 5,SYNDROMIC MR WITH ATAXIA DYSARTHRIA AND EPILEPSY,Syndromic multisystem autoimmune disease due to Itch deficiency,Syndromic Neurodevelopmental Disorder,Syndromic Neurodevelopmental Disorder with Corpus Collosum Axon Cardiac Ocular and Genital Defects,Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism,Syndromic neutropenia with Shwachman-Diamond-like features,Syndromic osteogenesis imperfecta,Syndromic recessive X-linked ichthyosis,Syndromic sensorineural deafness due to combined oxidative phosphorylation defect,syndromic X-linked intellectual disability,Syndromic X-linked intellectual disability due to JARID1C mutation,SYNGAP1-related developmental and epileptic encephalopathy,Synovial sarcoma,SYNPOLYDACTYLY 1,SYNPOLYDACTYLY 2,SYNPOLYDACTYLY 3/3-PRIME/4 ASSOCIATED WITH METACARPAL AND METATARSAL SYNOSTOSES,Synpolydactyly type 1,Synpolydactyly type 2,Syringocystadenoma Papilliferum,Systemic lupus erythematosus,SYSTEMIC LUPUS ERYTHEMATOSUS 16,SYSTEMIC LUPUS ERYTHEMATOSUS SUSCEPTIBILITY TO 1,SYSTEMIC LUPUS ERYTHEMATOSUS SUSCEPTIBILITY TO 10,SYSTEMIC LUPUS ERYTHEMATOSUS SUSCEPTIBILITY TO 11,SYSTEMIC LUPUS ERYTHEMATOSUS SUSCEPTIBILITY TO 2,SYSTEMIC LUPUS ERYTHEMATOSUS SUSCEPTIBILITY TO 9,Systemic mastocytosis with associated hematologic neoplasm,Systemic primary carnitine deficiency,Systemic-onset juvenile idiopathic arthritis,SYT2-related congenital onset presynaptic myasthenic syndrome,T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta,T-B+ severe combined immunodeficiency due to CD45 deficiency,T-B+ severe combined immunodeficiency due to gamma chain deficiency,T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency,T-B+ severe combined immunodeficiency due to JAK3 deficiency,T-CELL IMMUNODEFICIENCY CONGENITAL ALOPECIA AND NAIL DYSTROPHY,T-cell immunodeficiency recurrent infections and autoimmunity with or without cardiac malformations,T-cell immunodeficiency with epidermodysplasia verruciformis,T-cell large granular lymphocyte leukemia,T-CELL LYMPHOMA SUBCUTANEOUS PANNICULITIS-LIKE,T-CELL LYMPHOPENIA INFANTILE WITH OR WITHOUT NAIL DYSTROPHY AUTOSOMAL DOMINANT,Takayasu arteritis,Takenouchi-Kosaki syndrome,Tall stature-intellectual disability-renal anomalies syndrome,Tall stature-scoliosis-macrodactyly of the great toes syndrome,TANC2-related neurodevelopmental and psychiatric disorders,TANGIER DISEASE,TARP syndrome,TARSAL-CARPAL COALITION SYNDROME,Tatton-Brown Rahman syndrome (OVERGROWTH SYNDROME WITH INTELLECTUAL DISABILITY),Tatton-Brown-rahman syndrome,TAY-SACHS DISEASE,Tay-Sachs disease B variant adult form,Tay-Sachs disease B variant infantile form,Tay-Sachs disease B variant juvenile form,TAY-SACHS DISEASE B1 VARIANT,TBC1D2B-related neurodevelopmental disorder,TBCK-related intellectual disability syndrome,TCF20 syndrome,TCF7L2-related developmental disorder monoallelic,TCR-alpha-beta-positive T-cell deficiency,TELANGIECTASIA HEREDITARY HEMORRHAGIC TYPE 1,TELANGIECTASIA HEREDITARY HEMORRHAGIC TYPE 2,TELANGIECTASIA HEREDITARY HEMORRHAGIC TYPE 5,Telangiectasia macularis eruptiva perstans,Telethonin-related  limb-girdle muscular dystrophy R7,TELO2 Syndromic Intellectual Disability Disorder,TELO2-related intellectual disability-neurodevelopmental disorder,Temperature-sensitive oculocutaneous albinism type 1,Temple barraister syndrome,Temple syndrome due to maternal uniparental disomy of chromosome 14,Temple syndrome due to paternal 14q32.2 hypomethylation,Temple syndrome due to paternal 14q32.2 microdeletion,TEMPLE-BARAITSER SYNDROME,Temtamy preaxial brachydactyly syndrome,Temtamy syndrome,Temtamy syndrome; coloboma hypoplastic corpus callosum and intellectual disability,TENORIO SYNDROME,TERATOCARCINOMA-DERIVED GROWTH FACTOR 1,TERMINAL OSSEOUS DYSPLASIA,Terminal osseous dysplasia-pigmentary defects syndrome,Tessier number 4 facial cleft,Tessier number 7 facial cleft,TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE,TESTICULAR GERM CELL TUMOR,Testicular regression syndrome,Testicular seminomatous germ cell tumor,TET3 DNA Demethylation Disorder biallelic,TET3 DNA Demethylation Disorder monoallelic,Tetra-Amelia Syndrome,Tetra-amelia with lung agenesis,TETRAAMELIA SYNDROME 1,TETRAAMELIA SYNDROME 2,Tetraamelia-multiple malformations syndrome,Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria,Tetralogy of Fallot,TFE3-related intellectual disability with pigmentary mosaicism,Thanatophoric dysplasia type 1,THANATOPHORIC DYSPLASIA TYPE 2,THANATOPHORIC DYSPLASIA TYPE I,THANATOPHORIC DYSPLASIA TYPE II,THAUVIN-ROBINET-FAIVRE SYNDROME,THIAMINE METABOLISM DYSFUNCTION SYNDROME 2,THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE),THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY TYPE),THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 EPISODIC ENCEPHALOPATHYTYPE,Thiamine-responsive encephalopathy,Thiamine-responsive maple syrup urine disease,THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME,Thiel-Behnke corneal dystrophy,THIOPURINES POOR METABOLISM OF 1,THIOPURINES POOR METABOLISM OF 2,THIOUREA TASTING,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome,Thomsen and Becker disease,Thoracolumbosacral spina bifida aperta,Thoracolumbosacral spina bifida cystica,THREE M SYNDROME 1,THREE M SYNDROME 2,Three M syndrome 3,THROMBOCYTHEMIA 1,THROMBOCYTHEMIA 2,THROMBOCYTHEMIA 3,Thrombocythemia with distal limb defects,THROMBOCYTOPENIA 1,THROMBOCYTOPENIA 2,THROMBOCYTOPENIA 3,Thrombocytopenia 4,Thrombocytopenia 5,THROMBOCYTOPENIA 6,THROMBOCYTOPENIA 7,THROMBOCYTOPENIA ANEMIA AND MYELOFIBROSIS,THROMBOCYTOPENIA WITH BETA-THALASSEMIA X-LINKED,Thrombocytopenia with congenital dyserythropoietic anemia,THROMBOCYTOPENIA X-LINKED WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA,THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME,Thrombomodulin-related bleeding disorder,THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE,THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY,THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY AUTOSOMAL DOMINANT,THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY AUTOSOMAL RECESSIVE,THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY AUTOSOMAL DOMINANT,THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY AUTOSOMAL RECESSIVE,THROMBOPHILIA DUE TO THROMBIN DEFECT,Thrombophilia due to thrombomodulin defect,THROMBOPHILIA FAMILIAL DUE TO DECREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR,THROMBOPHILIA X-LINKED DUE TO FACTOR IX DEFECT,THROMBOTIC THROMBOCYTOPENIC PURPURA HEREDITARY,THYROID CANCER NONMEDULLARY 1,THYROID CANCER NONMEDULLARY 2,THYROID CANCER NONMEDULLARY 4,THYROID CANCER NONMEDULLARY 5,THYROID CARCINOMA FAMILIAL MEDULLARY,THYROID CARCINOMA HURTHLE CELL,THYROID DYSHORMONOGENESIS 1,THYROID DYSHORMONOGENESIS 2A,THYROID DYSHORMONOGENESIS 3,THYROID DYSHORMONOGENESIS 4,THYROID DYSHORMONOGENESIS 5,THYROID DYSHORMONOGENESIS 6,Thyroid ectopia,THYROID HORMONE METABOLISM ABNORMAL,THYROID HORMONE RESISTANCE GENERALIZED AUTOSOMAL DOMINANT,THYROID HORMONE RESISTANCE GENERALIZED AUTOSOMAL RECESSIVE,THYROID HORMONE RESISTANCE SELECTIVE PITUITARY,Thyroid Hormonogenesis Defect I,Thyroid hypoplasia,THYROID-STIMULATING HORMONE RECEPTOR,Thyrotoxic periodic paralysis,THYROTOXIC PERIODIC PARALYSIS SUSCEPTIBILITY TO 1,THYROTOXIC PERIODIC PARALYSIS SUSCEPTIBILITY TO 2,THYROTROPIN-RELEASING HORMONE DEFICIENCY,THYROXINE-BINDING GLOBULIN QUANTITATIVE TRAIT LOCUS,TIBIA HYPOPLASIA OR APLASIA OF WITH POLYDACTYLY,Tibial aplasia-ectrodactyly syndrome,Tibial hemimelia,Tibial muscular dystrophy,TIBIAL MUSCULAR DYSTROPHY TARDIVE,TIETZ ALBINISM-DEAFNESS SYNDROME,Tietz syndrome,TIMOTHY SYNDROME,Titin-related  limb-girdle muscular dystrophy R10,TKFC-related Cataracts and Multisystem Disease,TLK2 syndrome,TMEM106B related hypomyelinating leukodystrophy,TMEM165-CDG,TMEM199-CDG,TMEM251-related skeletal dysplasia,TMEM70-related mitochondrial encephalo-cardio-myopathy,TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome,TN POLYAGGLUTINATION SYNDROME,TNP03-related  limb-girdle muscular dystrophy D2,TNRC6B-related neurodevelopmental disorder,TOBACCO ADDICTION SUSCEPTIBILITY TO,TOE SYNDACTYLY TELECANTHUS AND ANOGENITAL AND RENAL MALFORMATIONS,TOGARAM1-related ciliopathy,TOLCHIN-LE CAIGNEC SYNDROME,TONNE-KALSCHEUER SYNDROME,Tooth agenesis,TOOTH AGENESIS SELECTIVE 1,TOOTH AGENESIS SELECTIVE 3,TOOTH AGENESIS SELECTIVE 4,Tooth agenesis selective 7,TOOTH AGENESIS SELECTIVE 8,TOOTH AGENESIS SELECTIVE 9,TOOTH AGENESIS SELECTIVE X-LINKED 1,tooth agenesis selective X-linked type 1,TOR1AIP1-related limb-girdle muscular dystrophy,Toriello-Carey syndrome,Toriello-Lacassie-Droste syndrome,Total early-onset cataract,Total spina bifida aperta,Total spina bifida cystica,TOWNES-BROCKS SYNDROME,TOWNES-BROCKS SYNDROME 1,TOWNES-BROCKS SYNDROME 2,TPP2-related immune deficiency autoimmune disease and intellectual disability,TRANSALDOLASE DEFICIENCY,Transcobalamin deficiency,TRANSCOBALAMIN II DEFICIENCY,TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2,TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN,Transient familial neonatal hyperbilirubinemia,Transient Hypomyelination during Infancy,Transient infantile hypertriglyceridemia and hepatosteatosis,Transient myeloproliferative syndrome,Transient neonatal diabetes mellitus,Transient Neonatal Hyperparathyroidism,Transketolase deficiency,Transposition of the great arteries dextro-looped 1,TRAPPC11-related  limb-girdle muscular dystrophy R18,TREACHER COLLINS SYNDROME 1,TREACHER COLLINS SYNDROME 2,TREACHER COLLINS SYNDROME 3,TREACHER COLLINS SYNDROME 4,TREACHER COLLINS SYNDROME TYPE 1,TREACHER COLLINS SYNDROME TYPE 2,Treacher-Collins syndrome,TREHALASE DEFICIENCY,TREMOR HEREDITARY ESSENTIAL 1,TREMOR HEREDITARY ESSENTIAL 4,Tremor hereditary essential 5,TREMOR HEREDITARY ESSENTIAL 6,Tremor-ataxia-central hypomyelination syndrome,Tricho-dento-osseous syndrome,TRICHO-RHINO-PHALANGEAL SYNDROME TYPE 1,TRICHODENTOOSSEOUS SYNDROME,TRICHOEPITHELIOMA MULTIPLE FAMILIAL 1,Trichohepatoenteric syndrome,TRICHOHEPATOENTERIC SYNDROME 1,TRICHOHEPATOENTERIC SYNDROME 2,Trichohepatoneurodevelopmental syndrome,Trichomegaly,Trichomegaly-retina pigmentary degeneration-dwarfism syndrome,Trichorhinophalangeal syndrome type 1 and 3,Trichorhinophalangeal syndrome type 2,TRICHORHINOPHALANGEAL SYNDROME TYPE I,TRICHORHINOPHALANGEAL SYNDROME TYPE III,Trichothiodystrophy,TRICHOTHIODYSTROPHY 1 PHOTOSENSITIVE,TRICHOTHIODYSTROPHY 2 PHOTOSENSITIVE,TRICHOTHIODYSTROPHY 3 PHOTOSENSITIVE,TRICHOTHIODYSTROPHY 4 NONPHOTOSENSITIVE,TRICHOTHIODYSTROPHY 5 NONPHOTOSENSITIVE,Trichothiodystrophy 6 nonphotosensitive,TRICHOTHIODYSTROPHY 7 NONPHOTOSENSITIVE,trichothiodystrophy non-photosensitive type 1,TRICHOTHIODYSTROPHY PHOTOSENSITIVE,Trichotillomania,Triglyceride deposit cardiomyovasculopathy,TRIGONOCEPHALY 1,TRIGONOCEPHALY 2,TRIM32-related  limb-girdle muscular dystrophy R8,TRIM8-related neurodevelopmental disorder,TRIMETHYLAMINURIA,TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME,TRIOSEPHOSPHATE ISOMERASE DEFICIENCY,TRIP12-related intellectual disability with/without autism spectrum disorder,TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME,Triple A syndrome,Trismus-pseudocamptodactyly syndrome,Trisomy Xq28,TRITANOPIA,tRNA isopentenyltransferase deficiency,TROPICAL CALCIFIC PANCREATITIS,Tropical pancreatitis,TRPM3-related developmental disorder monoallelic,TRUNCUS ARTERIOSIS,TRUNCUS ARTERIOSUS,TSH-secreting pituitary adenoma,TTC12-related Primary Ciliary Dyskinesia,TTC5-associated neurodevelopmental disorder,Tuberculosis,Tuberous sclerosis 1,Tuberous sclerosis 2,Tuberous sclerosis complex,TUBEROUS SCLEROSIS TYPE 1,TUBEROUS SCLEROSIS TYPE 2,Tubular-Aggregate Myopathy,Tubulinopathy-associated dysgyria,TUBULOINTERSTITIAL KIDNEY DISEASE AUTOSOMAL DOMINANT 1,TUBULOINTERSTITIAL KIDNEY DISEASE AUTOSOMAL DOMINANT 2,TUBULOINTERSTITIAL KIDNEY DISEASE AUTOSOMAL DOMINANT 4,TUBULOINTERSTITIAL KIDNEY DISEASE AUTOSOMAL DOMINANT 5,Tufted angioma,Tumor necrosis factor receptor 1 associated periodic syndrome,TUMOR PREDISPOSITION SYNDROME,TUMORAL CALCINOSIS HYPERPHOSPHATEMIC FAMILIAL 1,TUMORAL CALCINOSIS HYPERPHOSPHATEMIC FAMILIAL 2,TUMORAL CALCINOSIS HYPERPHOSPHATEMIC FAMILIAL 3,TUMORAL CALCINOSIS NORMOPHOSPHATEMIC FAMILIAL,Turcot syndrome with polyposis,TURNPENNY-FRY SYNDROME,TWINNING DIZYGOTICOVARIAN RESPONSE TO FSH STIMULATION INCLUDED,TYLOSIS WITH ESOPHAGEAL CANCER,TYPE 1 DIABETES MELLITUS,TYPE 1 DIABETES MELLITUS 10,TYPE 1 DIABETES MELLITUS 12,TYPE 1 DIABETES MELLITUS 2,TYPE 1 DIABETES MELLITUS 20,TYPE 1 DIABETES MELLITUS 22,TYPE 1 DIABETES MELLITUS 5,TYPE 2 DIABETES 5,TYPE 2 DIABETES MELLITUS,TYPE 2 DIABETES MELLITUS 1,Typical nemaline myopathy,Typical urticaria pigmentosa,Tyrosinemia type 1,Tyrosinemia type 2,Tyrosinemia type 3,TYROSINEMIA TYPE I,TYROSINEMIA TYPE II,TYROSINEMIA TYPE III,U2AF2-related developmental disorder monoallelic,UBE2A-Related X-Linked Syndromic Mental Retardation,UBE4A-associated neurodevelopmental disorder,UGP2 Epileptic Encephalopathy,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1,Ullrich congenital muscular dystrophy 2,Ulna and fibula absence of with severe limb deficiency,ULNAR-MAMMARY SYNDROME,UMOD-related autosomal dominant tubulointerstitial kidney disease,UNC119 LIPID-BINDING CHAPERONE,UNC45B-associated Progressive Myopathy with Eccentric Cores,UNCOMBABLE HAIR SYNDROME,UNCOMBABLE HAIR SYNDROME 1,Uncombable hair syndrome 2,UNCOMBABLE HAIR SYNDROME 3,Unilateral multicystic dysplastic kidney,Unspecified Neurodevelopmental Disorder,Unverricht-Lundborg disease,UPF1-related developmental disorder monoallelic,Upper thoracic spina bifida aperta,Upper thoracic spina bifida cystica,URIC ACID CONCENTRATION SERUM QUANTITATIVE TRAIT LOCUS 1,URIC ACID CONCENTRATION SERUM QUANTITATIVE TRAIT LOCUS 4,Uridine 5-prime monophosphate hydrolase deficiency hemolytic anemia due to,URIDINE-CYTIDINEURIA,Uridine-responsive epileptic encephalopathy,UROCANASE DEFICIENCY,Urocanic aciduria,UROFACIAL SYNDROME,UROFACIAL SYNDROME 1,UROFACIAL SYNDROME 2,URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME,Usher syndrome,Usher syndrome type 1,USHER SYNDROME TYPE 1D,USHER SYNDROME TYPE 1J,USHER SYNDROME TYPE 1M,Usher syndrome type 2,Usher syndrome type 3,USHER SYNDROME TYPE I,USHER SYNDROME TYPE IC,USHER SYNDROME TYPE ID,USHER SYNDROME TYPE IF,USHER SYNDROME TYPE IG,USHER SYNDROME TYPE IIA,USHER SYNDROME TYPE IIC,USHER SYNDROME TYPE IID,USHER SYNDROME TYPE IIIA,USHER SYNDROME TYPE IIIB,USHER SYNDROME TYPE IJ,USHER SYNDROME TYPE IV,USP18 deficiency,USP7-related developmental disorder monoallelic,UV-sensitive syndrome,UV-SENSITIVE SYNDROME 1,UV-SENSITIVE SYNDROME 2,UV-SENSITIVE SYNDROME 3,Uveal coloboma - cleft lip and palate - intellectual disability,Uveal melanoma,VACTERL Association X-Linked with or without Hydrocephalus,VACTERL with hydrocephalus,VACTERL/VATER association,Vacuolar myopathy with sarcoplasmic reticulum protein aggregates,Van Buchem disease type 2,Van den Ende-Gupta syndrome,Van der Woude syndrome,VAN DER WOUDE SYNDROME 1,VAN DER WOUDE SYNDROME 2,VAN ESCH-ODRISCOLL SYNDROME,VAN MALDERGEM SYNDROME,VAN MALDERGEM SYNDROME 1,Van Maldergem syndrome 2,VANIN 1,Variable Neurodevelopmental Disorder,Variant ABeta2M amyloidosis,VARIEGATE PORPHYRIA,VAS DEFERENS CONGENITAL BILATERAL APLASIA OF,VAS DEFERENS CONGENITAL BILATERAL APLASIA OF X-LINKED,Vascular Ehlers-Danlos syndrome,VASCULAR MALFORMATION PRIMARY INTRAOSSEOUS,VASCULITIS AUTOINFLAMMATION IMMUNODEFICIENCY AND HEMATOLOGICDEFECTS SYNDROME,Vasculitis due to ADA2 deficiency,VASCULOPATHY RETINAL WITH CEREBRAL LEUKOENCEPHALOPATHY AND SYSTEMIC MANIFESTATIONS,VCP-related developmental disorder monoallelic,Vein of Galen aneurysmal malformation,VELOCARDIOFACIAL SYNDROME,VENOUS MALFORMATIONS MULTIPLE CUTANEOUS AND MUCOSAL,VENTRICULAR FIBRILLATION PAROXYSMAL FAMILIAL 1,VENTRICULAR FIBRILLATION PAROXYSMAL FAMILIAL 2,VENTRICULAR SEPTAL DEFECT 1,VENTRICULAR SEPTAL DEFECT 2,VENTRICULAR SEPTAL DEFECT 3,VENTRICULAR TACHYCARDIA CATECHOLAMINERGIC POLYMORPHIC 1 WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY,VENTRICULAR TACHYCARDIA CATECHOLAMINERGIC POLYMORPHIC 2,VENTRICULAR TACHYCARDIA CATECHOLAMINERGIC POLYMORPHIC 3,VENTRICULAR TACHYCARDIA CATECHOLAMINERGIC POLYMORPHIC 4,Ventricular tachycardia catecholaminergic polymorphic 5 with or without muscle weakness,VENTRICULAR TACHYCARDIA FAMILIAL,Ventriculomegaly with cystic kidney disease,Ventriculomegaly-cystic kidney disease,Verheij syndrome,VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION,VERTEBRAL CARDIAC RENAL AND LIMB DEFECTS SYNDROME 1,VERTEBRAL CARDIAC RENAL AND LIMB DEFECTS SYNDROME 2,VERTEBRAL CARDIAC RENAL AND LIMB DEFECTS SYNDROME 3,VERTEBRAL CARDIAC TRACHEOESOPHAGEAL RENAL AND LIMB DEFECTS,VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES,VERTICAL TALUS CONGENITAL,VERVERI-BRADY SYNDROME,Very long chain acyl-CoA dehydrogenase deficiency,Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency,VESICOURETERAL REFLUX 2,VESICOURETERAL REFLUX 3,Vesicoureteral reflux 8,vesicoureteral reflux type 3,VEXAS SYNDROME,VIBRATORY URTICARIA,Vici syndrome,Viral induced severe multiorgan dysfunction associated with impaired mitochondrial fission,Visceral myopathy,VISSERS-BODMER SYNDROME,VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI,VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1,Vitamin B12-responsive methylmalonic acidemia type cblA,Vitamin B12-responsive methylmalonic acidemia type cblB,Vitamin B12-responsive methylmalonic acidemia type cblDv2,Vitamin B12-unresponsive methylmalonic acidemia type mut-,Vitamin B12-unresponsive methylmalonic acidemia type mut0,VITAMIN D HYDROXYLATION-DEFICIENT RICKETS TYPE 1A,VITAMIN D HYDROXYLATION-DEFICIENT RICKETS TYPE 1B,VITAMIN D-DEPENDENT RICKETS TYPE 2A,VITAMIN D-DEPENDENT RICKETS TYPE 3,VITAMIN K-DEPENDENT CLOTTING FACTORS COMBINED DEFICIENCY OF 1,VITAMIN K-DEPENDENT CLOTTING FACTORS COMBINED DEFICIENCY OF 2,Vitamin-B6-Dependent Epilepsy,Vitiligo-associated multiple autoimmune disease susceptibility 1,VITREORETINAL DEGENERATION SNOWFLAKE TYPE,VITREORETINOCHOROIDOPATHY,VITREORETINOPATHY EXUDATIVE TYPE 4,VITREORETINOPATHY NEOVASCULAR INFLAMMATORY,VITREORETINOPATHY WITH PHALANGEAL EPIPHYSEAL DYSPLASIA,Vocal cord and pharyngeal distal myopathy,Vogt-Koyanagi-Harada disease,VOHWINKEL SYNDROME,VOHWINKEL SYNDROME VARIANT FORM,Von Hippel-Lindau disease,VON HIPPEL-LINDAU SYNDROME,von Willebrand disease type 1,VON WILLEBRAND DISEASE TYPE 2,Von Willebrand disease type 2A,VON WILLEBRAND DISEASE TYPE 2B,von Willebrand disease type 2M,von Willebrand disease type 2N,von Willebrand disease type 3,VPS11-related autosomal recessive hypomyelinating leukodystrophy,VULTO-VAN SILFHOUT-DE VRIES SYNDROME,WAARDENBURG SYNDROME TYPE 1,Waardenburg syndrome type 2,WAARDENBURG SYNDROME TYPE 2A,WAARDENBURG SYNDROME TYPE 2D,WAARDENBURG SYNDROME TYPE 2E,Waardenburg syndrome type 3,WAARDENBURG SYNDROME TYPE 4A,WAARDENBURG SYNDROME TYPE 4B,WAARDENBURG SYNDROME TYPE 4C,Waardenburg-Shah syndrome,Wagner disease,WAGNER VITREORETINOPATHY,WAGR syndrome,WAISMAN SYNDROME,Waldenstrom macroglobulinemia,WALKER WARBERG SYNDROME,Walker-Warburg syndrome,WARBURG MICRO SYNDROME 1,WARBURG MICRO SYNDROME 2,WARBURG MICRO SYNDROME 3,Warburg micro syndrome 4,Warburg micro syndrome type 1,Warburg micro syndrome type 3,Warburg-Cinotti syndrome,WARFARIN SENSITIVITY X-LINKED,WARS2-related combined oxidative phosphorylation defect,WARSAW BREAKAGE SYNDROME,WATSON SYNDROME,WDR45-RELATED NEURODEGENERATION WITH BRAIN IRON ACCUMULATION,Weaver syndrome,WEAVER SYNDROME 2,Weaver-like overgrowth syndrome,WEBB-DATTANI SYNDROME,Weill-Marchesani syndrome,WEILL-MARCHESANI SYNDROME 1,WEILL-MARCHESANI SYNDROME 2,WEILL-MARCHESANI SYNDROME 3,WEILL-MARCHESANI SYNDROME 4,WEILL-MARCHESANI SYNDROME AUTOSOMAL DOMINANT,WEISS-KRUSZKA SYNDROME,WELANDER DISTAL MYOPATHY,Well-differentiated liposarcoma,Werner Syndrome,WEST NILE VIRUS SUSCEPTIBILITY TO,WEYERS ACROFACIAL DYSOSTOSIS,WHIM SYNDROME,WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1,WHITE SPONGE NEVUS,WHITE SPONGE NEVUS 1,WHITE SPONGE NEVUS 2,WHITE-SUTTON SYNDROME,Wieacker-Wolff syndrome,WIEACKER-WOLFF SYNDROME FEMALE-RESTRICTED,WIEDEMANN-RAUTENSTRAUCH SYNDROME,Wiedemann-Steiner syndrome,Williams syndrome,WILLIAMS-BEUREN SYNDROME,WILMS TUMOR 1,WILMS TUMOR 5,Wilms tumor 6,Wilms tumor aniridia genitourinary anomalies and mental retardation syndrome,WILSON DISEASE,Wilson-Turner syndrome,WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME,Winchester syndrome,WISKOTT-ALDRICH SYNDROME,WISKOTT-ALDRICH SYNDROME 2,WITKOP SYNDROME,Witteveen-kolk syndrome,WNT5A-Related Robinow Syndrome Autosomal Dominant,WNT7A- associated skeletal malformations syndrome,WOLCOTT-RALLISON SYNDROME,Wolf-Hirschhorn syndrome,WOLFF-PARKINSON-WHITE SYNDROME,Wolfram syndrome,WOLFRAM SYNDROME 1,WOLFRAM SYNDROME 2,Wolfram syndrome type 2,Wolfram-like syndrome,WOLFRAM-LIKE SYNDROME AUTOSOMAL DOMINANT,WOLMAN DISEASE,WOODHOUSE-SAKATI SYNDROME,Woolly hair,WOOLLY HAIR AUTOSOMAL DOMINANT,WOOLLY HAIR AUTOSOMAL RECESSIVE 3,Woolly Hair Liver Dysfunction Dysmorphic Features and Global Developmental Delay,Woolly hair nevus,Woolly hair-palmoplantar keratoderma syndrome,WRINKLY SKIN SYNDROME,X INACTIVATION FAMILIAL SKEWED 1,X-linked adrenal hypoplasia congenita,X-linked agammaglobulinemia,X-linked Alport syndrome,X-linked Alport syndrome-diffuse leiomyomatosis,X-linked anophthalmia syndrome,X-linked central congenital hypothyroidism with late-onset testicular enlargement,X-linked centronuclear myopathy,X-linked cerebral adrenoleukodystrophy,X-linked Charcot-Marie-Tooth disease type 1,X-linked Charcot-Marie-Tooth disease type 4,X-linked Charcot-Marie-Tooth disease type 5,X-linked Charcot-Marie-Tooth disease type 6,X-linked cleft palate and ankyloglossia,X-linked complicated corpus callosum dysgenesis,X-linked complicated spastic paraplegia type 1,X-linked cone dysfunction syndrome with myopia,X-linked congenital generalized hypertrichosis,X-LINKED CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION,X-LINKED CREATINE DEFICIENCY SYNDROME,X-linked creatine transporter deficiency,X-linked distal spinal muscular atrophy type 3,X-linked dominant chondrodysplasia Chassaing-Lacombe type,X-linked dominant chondrodysplasia punctata,X-linked dyserythropoietic anemia with abnormal platelets and neutropenia,X-linked dystonia-parkinsonism,X-linked Ehlers-Danlos syndrome,X-linked Emery-Dreifuss muscular dystrophy,X-linked epilepsy-learning disabilities-behavior disorders syndrome,X-linked erythropoietic protoporphyria,X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome,X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability,X-linked hereditary sensory and autonomic neuropathy with deafness,X-linked hyper-IgM syndrome,X-linked hypohidrotic ectodermal dysplasia,X-Linked Hypophosphatemia,X-LINKED HYPOSPADIAS TYPE 2,X-linked immunodeficiency with magnesium defect Epstein-Barr virus infection and neoplasia,X-linked intellectual disability Cabezas type,X-linked intellectual disability Cantagrel type,X-linked intellectual disability due to GRIA3 mutations,X-linked intellectual disability Golabi-Ito-Hall type,X-linked intellectual disability Hedera type,X-linked intellectual disability Najm type,X-linked intellectual disability Nascimento type,X-linked intellectual disability Porteous type,X-linked intellectual disability Siderius type,X-linked intellectual disability Snyder type,X-linked intellectual disability Stocco Dos Santos type,X-linked intellectual disability Sutherland-Haan type,X-linked intellectual disability Van Esch type,X-linked intellectual disability with isolated growth hormone deficiency,X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome,X-linked intellectual disability-cerebellar hypoplasia syndrome,X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome,X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome,X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome,X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome,X-linked intellectual disability-hypotonia-movement disorder syndrome,X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome,X-linked intellectual disability-psychosis-macroorchidism syndrome,X-linked intellectual disability-short stature-overweight syndrome,X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome,X-linked lissencephaly with abnormal genitalia,X-linked lymphoproliferative disease due to SH2D1A deficiency,X-linked lymphoproliferative disease due to XIAP deficiency,X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency,X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency,X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome,X-linked myopathy with excessive autophagy,X-linked myopathy with postural muscle atrophy,X-linked myotubular myopathy-abnormal genitalia syndrome,X-linked non progressive cerebellar ataxia,X-linked non-syndromic intellectual disability,X-linked nonsyndromic sensorineural deafness type DFN,X-linked osteoporosis with fractures,X-linked parkinsonism-spasticity syndrome,X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects,X-linked progressive cerebellar ataxia,X-linked recessive ocular albinism,X-linked reticulate pigmentary disorder,X-linked retinoschisis,X-linked scapuloperoneal muscular dystrophy,X-linked severe congenital neutropenia,X-linked sideroblastic anemia,X-linked sideroblastic anemia and spinocerebellar ataxia,X-linked spasticity-intellectual disability-epilepsy syndrome,X-Linked Spondyloepimetaphyseal Dysplasia,X-linked thrombocytopenia with normal platelets,X-LINKED TRICHOTHIODYSTROPHY,Xanthinuria type I,Xanthinuria type II,Xeroderma pigmentosum,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP A,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP B,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP C,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP D,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP E,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP F,XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP G,Xeroderma pigmentosum group A,Xeroderma pigmentosum group C,XERODERMA PIGMENTOSUM GROUP E DDB-NEGATIVE SUBTYPE,Xeroderma pigmentosum variant,XERODERMA PIGMENTOSUM VARIANT TYPE,Xeroderma pigmentosum-Cockayne syndrome complex,XFE PROGEROID SYNDROME,Xia-Gibbs syndrome,XL Intellectual disability,Xq21 microdeletion syndrome,Xq25 microduplication syndrome,Xq27.3q28 duplication syndrome,XYLT1-CDG,YAO SYNDROME,YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME,YOU-HOOVER-FONG SYNDROME,Young adult-onset distal hereditary motor neuropathy,Young-onset Parkinson disease,YT BLOOD GROUP ANTIGEN,YUNIS-VARON SYNDROME,ZBTB18 syndrome,ZBTB7A-associated developmental disorder,Zebra body myopathy,Zellweger Syndrome,ZFHX3-related developmental disorder monoallelic,ZFHX4-related developmental disorder monoallelic,ZFPM2-associated malformation syndrome,Zimmermann-Laband syndrome,ZIMMERMANN-LABAND SYNDROME 1,ZIMMERMANN-LABAND SYNDROME 2,ZIMMERMANN-LABAND SYNDROME 3,ZINC DEFICIENCY TRANSIENT NEONATAL,ZINC FINGER PROTEIN 106,ZMYM2-related developmental disorder monoallelic,ZNF148-related developmental disorder monoallelic,ZNF292-related developmental disorder monoallelic,ZNF407-related Neurodevelopmental Disorder,ZTTK SYNDROME,ZUNICH NEUROECTODERMAL SYNDROME,Zygodactyly type 3]", 
          "[DDG2P,MIM morbid,Orphanet]", "[]", "[]", "[EXP,HDA,HEP,HMP,IBA,IC,IDA,IEA,IEP,IGI,IMP,IPI,ISA,ISM,ISO,ISS,NAS,ND,RCA,TAS]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", "[]", 
          "[ClinVar,dbSNP,HGMD-PUBLIC]", "[only,excluded]", "[3_prime_UTR_variant,5_prime_UTR_variant,coding_sequence_variant,coding_transcript_variant,downstream_gene_variant,exon_variant,feature_ablation,feature_amplification,feature_elongation,feature_truncation,feature_variant,frameshift_variant,gene_variant,incomplete_terminal_codon_variant,inframe_deletion,inframe_indel,inframe_insertion,inframe_variant,intergenic_variant,internal_feature_elongation,intron_variant,mature_miRNA_variant,missense_variant,NMD_transcript_variant,nonsynonymous_variant,non_coding_transcript_exon_variant,non_coding_transcript_variant,protein_altering_variant,sequence_comparison,sequence_variant,splice_acceptor_variant,splice_donor_variant,splice_region_variant,splice_site_variant,splicing_variant,start_lost,stop_gained,stop_lost,stop_retained_variant,structural_variant,synonymous_variant,terminator_codon_variant,transcript_ablation,transcript_amplification,transcript_variant,upstream_gene_variant,UTR_variant]"
          ), fullDescription = c("", "Determine which base pair on the specified chromosome/scaffold to begin range", 
          "Determine which base pair on the specified chromosome/scaffold to end range", 
          "", "Limit to Genes within multiple comma separate Chromosomal regions (1:100:10000:-1,1:100000:2000000:1)", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "Filter to include genes with supplied list of Gene stable ID(s)", 
          "Filter to include genes with supplied list of Gene stable ID(s) with version", 
          "Filter to include genes with supplied list of Transcript stable ID(s)", 
          "Filter to include genes with supplied list of Transcript stable ID(s) with version", 
          "Filter to include genes with supplied list of Protein stable ID(s)", 
          "Filter to include genes with supplied list of Protein stable ID(s) with version", 
          "Filter to include genes with supplied list of Exon ID(s)", 
          "Filter to include genes with supplied list of Gene Name(s)", 
          "Filter to include genes with supplied list of Transcript Name(s)", 
          "Filter to include genes with supplied list of Gene Synonym(s)", 
          "Filter to include genes with supplied list of BioGRID Interaction data, The General Repository for Interaction Datasets ID(s)", 
          "Filter to include genes with supplied list of CCDS ID(s)", 
          "Filter to include genes with supplied list of ChEMBL ID(s)", 
          "Filter to include genes with supplied list of DataBase of Aberrant 3' Splice Sites name(s)", 
          "Filter to include genes with supplied list of DataBase of Aberrant 3' Splice Sites ID(s)", 
          "Filter to include genes with supplied list of DataBase of Aberrant 5' Splice Sites name(s)", 
          "Filter to include genes with supplied list of DataBase of Aberrant 5' Splice Sites ID(s)", 
          "Filter to include genes with supplied list of Ensembl Human Transcript ID(s)", 
          "Filter to include genes with supplied list of Ensembl Human Translation ID(s)", 
          "Filter to include genes with supplied list of EntrezGene transcript name ID(s)", 
          "Filter to include genes with supplied list of European Nucleotide Archive ID(s)", 
          "Filter to include genes with supplied list of Expression Atlas ID(s)", 
          "Filter to include genes with supplied list of GeneDB ID(s)", 
          "Filter to include genes with supplied list of GO ID(s)", 
          "Filter to include genes with supplied list of GOSlim GOA ID(s)", 
          "Filter to include genes with supplied list of HGNC ID(s)", 
          "Filter to include genes with supplied list of HGNC symbol(s)", 
          "Filter to include genes with supplied list of Human Protein Atlas accession(s)", 
          "Filter to include genes with supplied list of Human Protein Atlas ID(s)", 
          "Filter to include genes with supplied list of INSDC protein ID ID(s)", 
          "Filter to include genes with supplied list of LRG display in Ensembl gene ID(s)", 
          "Filter to include genes with supplied list of LRG display in Ensembl transcript ID(s)", 
          "Filter to include genes with supplied list of MEROPS - the Peptidase Database ID(s)", 
          "Filter to include genes with supplied list of MIM gene accession(s)", 
          "Filter to include genes with supplied list of MIM morbid accession(s)", 
          "Filter to include genes with supplied list of miRBase accession(s)", 
          "Filter to include genes with supplied list of miRBase ID(s)", 
          "Filter to include genes with supplied list of miRBase transcript name ID(s)", 
          "Filter to include genes with supplied list of NCBI gene (formerly Entrezgene) accession(s)", 
          "Filter to include genes with supplied list of NCBI gene (formerly Entrezgene) ID(s)", 
          "Filter to include genes with supplied list of PDB ID(s)", 
          "Filter to include genes with supplied list of Reactome ID(s)", 
          "Filter to include genes with supplied list of Reactome gene ID(s)", 
          "Filter to include genes with supplied list of Reactome transcript ID(s)", 
          "Filter to include genes with supplied list of RefSeq mRNA ID(s)", 
          "Filter to include genes with supplied list of RefSeq mRNA predicted ID(s)", 
          "Filter to include genes with supplied list of RefSeq ncRNA ID(s)", 
          "Filter to include genes with supplied list of RefSeq ncRNA predicted ID(s)", 
          "Filter to include genes with supplied list of RefSeq peptide ID(s)", 
          "Filter to include genes with supplied list of RefSeq peptide predicted ID(s)", 
          "Filter to include genes with supplied list of RFAM ID(s)", 
          "Filter to include genes with supplied list of RFAM transcript name ID(s)", 
          "Filter to include genes with supplied list of RNAcentral ID(s)", 
          "Filter to include genes with supplied list of Transcript name ID(s)", 
          "Filter to include genes with supplied list of UCSC Stable ID ID(s)", 
          "Filter to include genes with supplied list of UniParc ID(s)", 
          "Filter to include genes with supplied list of UniProtKB Gene Name symbol(s)", 
          "Filter to include genes with supplied list of UniProtKB Gene Name ID(s)", 
          "Filter to include genes with supplied list of UniProtKB isoform ID(s)", 
          "Filter to include genes with supplied list of UniProtKB/Swiss-Prot ID(s)", 
          "Filter to include genes with supplied list of UniProtKB/TrEMBL ID(s)", 
          "Filter to include genes with supplied list of WikiGene name(s)", 
          "Filter to include genes with supplied list of WikiGene ID(s)", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "Filter to include genes with supplied list of AFFY HC G110 ID(s)", 
          "Filter to include genes with supplied list of AFFY HG Focus ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U133A ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U133A 2 ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U133B ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U133 Plus 2 ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95A ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95Av2 ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95B ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95C ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95D ID(s)", 
          "Filter to include genes with supplied list of AFFY HG U95E ID(s)", 
          "Filter to include genes with supplied list of AFFY HTA 2 0 ID(s)", 
          "Filter to include genes with supplied list of AFFY HuEx 1 0 st v2 ID(s)", 
          "Filter to include genes with supplied list of AFFY HuGeneFL ID(s)", 
          "Filter to include genes with supplied list of AFFY HuGene 1 0 st v1 ID(s)", 
          "Filter to include genes with supplied list of AFFY HuGene 2 0 st v1 ID(s)", 
          "Filter to include genes with supplied list of AFFY HuGene 2 1 st v1 ID(s)", 
          "Filter to include genes with supplied list of AFFY PrimeView ID(s)", 
          "Filter to include genes with supplied list of AFFY U133 X3P ID(s)", 
          "Filter to include genes with supplied list of AGILENT CGH 44b ID(s)", 
          "Filter to include genes with supplied list of AGILENT GPL26966 ID(s)", 
          "Filter to include genes with supplied list of AGILENT GPL6848 ID(s)", 
          "Filter to include genes with supplied list of AGILENT SurePrint G3 GE 8x60k ID(s)", 
          "Filter to include genes with supplied list of AGILENT SurePrint G3 GE 8x60k v2 ID(s)", 
          "Filter to include genes with supplied list of AGILENT WholeGenome ID(s)", 
          "Filter to include genes with supplied list of AGILENT WholeGenome 4x44k v1 ID(s)", 
          "Filter to include genes with supplied list of AGILENT WholeGenome 4x44k v2 ID(s)", 
          "Filter to include genes with supplied list of CODELINK CODELINK ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanHT 12 V3 ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanHT 12 V4 ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanRef 8 V3 ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanWG 6 V1 ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanWG 6 V2 ID(s)", 
          "Filter to include genes with supplied list of ILLUMINA HumanWG 6 V3 ID(s)", 
          "Filter to include genes with supplied list of PHALANX OneArray ID(s)", 
          "Limit to genes within given Transcript Count range", 
          "Limit to genes within given Transcript Count range", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "Filter to include genes with supplied list of Interpro", 
          "Filter to include genes with supplied list of CDD ID(s)", 
          "Filter to include genes with supplied list of Gene3D ID(s)", 
          "Filter to include genes with supplied list of HAMAP ID(s)", 
          "Filter to include genes with supplied list of PANTHER ID(s)", 
          "Filter to include genes with supplied list of Pfam ID(s)", 
          "Filter to include genes with supplied list of PIRSF ID(s)", 
          "Filter to include genes with supplied list of Prints ID(s)", 
          "Filter to include genes with supplied list of PROSITE patterns ID(s)", 
          "Filter to include genes with supplied list of PROSITE profiles ID(s)", 
          "Filter to include genes with supplied list of SFLD ID(s)", 
          "Filter to include genes with supplied list of SMART ID(s)", 
          "Filter to include genes with supplied list of Superfamily ID(s)", 
          "Filter to include genes with supplied list of TIGRFAM ID(s)", 
          "", "Entries associated with variants that have been validated", 
          ""), filters = c("filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters", 
          "filters", "filters", "filters", "filters", "filters"
          ), type = c("text", "text", "text", "text", "text", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "text", "text", 
          "list", "list", "list", "list", "boolean", "boolean", 
          "boolean", "boolean", "boolean", "boolean", "list", "list", 
          "list", "text", "list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "boolean_list", "boolean_list", 
          "boolean_list", "boolean_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "id_list", "id_list", "id_list", 
          "id_list", "id_list", "list", "boolean", "list"), operation = c("=", 
          ">=", "<=", "=", "=", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          ">=", "<=", "=", "=", "=", "=", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "=", "=", "=", "=", "=,in", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "only,excluded", "only,excluded", 
          "only,excluded", "only,excluded", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", "=,in", 
          "=,in", "=,in", "=,in", "=,in", "=", "only,excluded", 
          "="), filters8 = c("hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main,hsapiens_gene_ensembl__gene__main,hsapiens_gene_ensembl__gene__main,hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__exon_transcript__dm", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__external_synonym__dm", "hsapiens_gene_ensembl__ox_biogrid__dm", 
          "hsapiens_gene_ensembl__ox_ccds__dm", "hsapiens_gene_ensembl__ox_chembl__dm", 
          "hsapiens_gene_ensembl__ox_dbass3__dm", "hsapiens_gene_ensembl__ox_dbass3__dm", 
          "hsapiens_gene_ensembl__ox_dbass5__dm", "hsapiens_gene_ensembl__ox_dbass5__dm", 
          "hsapiens_gene_ensembl__ox_ens_hs_transcript__dm", "hsapiens_gene_ensembl__ox_ens_hs_translation__dm", 
          "hsapiens_gene_ensembl__ox_entrezgene_trans_name__dm", 
          "hsapiens_gene_ensembl__ox_embl__dm", "hsapiens_gene_ensembl__ox_arrayexpress__dm", 
          "hsapiens_gene_ensembl__ox_genedb__dm", "hsapiens_gene_ensembl__ox_go__dm", 
          "hsapiens_gene_ensembl__ox_goslim_goa__dm", "hsapiens_gene_ensembl__ox_hgnc__dm", 
          "hsapiens_gene_ensembl__ox_hgnc__dm", "hsapiens_gene_ensembl__ox_hpa__dm", 
          "hsapiens_gene_ensembl__ox_hpa__dm", "hsapiens_gene_ensembl__ox_protein_id__dm", 
          "hsapiens_gene_ensembl__ox_ens_lrg_gene__dm", "hsapiens_gene_ensembl__ox_ens_lrg_transcript__dm", 
          "hsapiens_gene_ensembl__ox_merops__dm", "hsapiens_gene_ensembl__ox_mim_gene__dm", 
          "hsapiens_gene_ensembl__ox_mim_morbid__dm", "hsapiens_gene_ensembl__ox_mirbase__dm", 
          "hsapiens_gene_ensembl__ox_mirbase__dm", "hsapiens_gene_ensembl__ox_mirbase_trans_name__dm", 
          "hsapiens_gene_ensembl__ox_entrezgene__dm", "hsapiens_gene_ensembl__ox_entrezgene__dm", 
          "hsapiens_gene_ensembl__ox_pdb__dm", "hsapiens_gene_ensembl__ox_reactome__dm", 
          "hsapiens_gene_ensembl__ox_reactome_gene__dm", "hsapiens_gene_ensembl__ox_reactome_transcript__dm", 
          "hsapiens_gene_ensembl__ox_refseq_mrna__dm", "hsapiens_gene_ensembl__ox_refseq_mrna_predicted__dm", 
          "hsapiens_gene_ensembl__ox_refseq_ncrna__dm", "hsapiens_gene_ensembl__ox_refseq_ncrna_predicted__dm", 
          "hsapiens_gene_ensembl__ox_refseq_peptide__dm", "hsapiens_gene_ensembl__ox_refseq_peptide_predicted__dm", 
          "hsapiens_gene_ensembl__ox_rfam__dm", "hsapiens_gene_ensembl__ox_rfam_trans_name__dm", 
          "hsapiens_gene_ensembl__ox_rnacentral__dm", "hsapiens_gene_ensembl__ox_hgnc_trans_name__dm", 
          "hsapiens_gene_ensembl__ox_ucsc__dm", "hsapiens_gene_ensembl__ox_uniparc__dm", 
          "hsapiens_gene_ensembl__ox_uniprot_gn__dm", "hsapiens_gene_ensembl__ox_uniprot_gn__dm", 
          "hsapiens_gene_ensembl__ox_uniprot_isoform__dm", "hsapiens_gene_ensembl__ox_uniprotswissprot__dm", 
          "hsapiens_gene_ensembl__ox_uniprotsptrembl__dm", "hsapiens_gene_ensembl__ox_wikigene__dm", 
          "hsapiens_gene_ensembl__ox_wikigene__dm", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__efg_affy_hc_g110__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_focus__dm", "hsapiens_gene_ensembl__efg_affy_hg_u133a__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_u133a_2__dm", "hsapiens_gene_ensembl__efg_affy_hg_u133b__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_u133_plus_2__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_u95a__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95av2__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_u95b__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95c__dm", 
          "hsapiens_gene_ensembl__efg_affy_hg_u95d__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95e__dm", 
          "hsapiens_gene_ensembl__efg_affy_hta_2_0__dm", "hsapiens_gene_ensembl__efg_affy_huex_1_0_st_v2__dm", 
          "hsapiens_gene_ensembl__efg_affy_hugenefl__dm", "hsapiens_gene_ensembl__efg_affy_hugene_1_0_st_v1__dm", 
          "hsapiens_gene_ensembl__efg_affy_hugene_2_0_st_v1__dm", 
          "hsapiens_gene_ensembl__efg_affy_hugene_2_1_st_v1__dm", 
          "hsapiens_gene_ensembl__efg_affy_primeview__dm", "hsapiens_gene_ensembl__efg_affy_u133_x3p__dm", 
          "hsapiens_gene_ensembl__efg_agilent_cgh_44b__dm", "hsapiens_gene_ensembl__efg_agilent_gpl26966__dm", 
          "hsapiens_gene_ensembl__efg_agilent_gpl6848__dm", "hsapiens_gene_ensembl__efg_agilent_sureprint_g3_ge_8x60k__dm", 
          "hsapiens_gene_ensembl__efg_agilent_sureprint_g3_ge_8x60k_v2__dm", 
          "hsapiens_gene_ensembl__efg_agilent_wholegenome__dm", 
          "hsapiens_gene_ensembl__efg_agilent_wholegenome_4x44k_v1__dm", 
          "hsapiens_gene_ensembl__efg_agilent_wholegenome_4x44k_v2__dm", 
          "hsapiens_gene_ensembl__efg_codelink_codelink__dm", "hsapiens_gene_ensembl__efg_illumina_humanht_12_v3__dm", 
          "hsapiens_gene_ensembl__efg_illumina_humanht_12_v4__dm", 
          "hsapiens_gene_ensembl__efg_illumina_humanref_8_v3__dm", 
          "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v1__dm", 
          "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v2__dm", 
          "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v3__dm", 
          "hsapiens_gene_ensembl__efg_phalanx_onearray__dm", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__tra_tsl__dm", 
          "hsapiens_gene_ensembl__tra_gencode_basic__dm", "hsapiens_gene_ensembl__tra_appris__dm", 
          "hsapiens_gene_ensembl__tra_is_canonical__dm", "hsapiens_gene_ensembl__tra_mane_select__dm", 
          "hsapiens_gene_ensembl__tra_mane_plus_clinical__dm", 
          "hsapiens_gene_ensembl__phenotype__dm", "hsapiens_gene_ensembl__phenotype__dm", 
          "pointer dataset", "pointer dataset", "hsapiens_gene_ensembl__ontology_go__dm", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
          "hsapiens_gene_ensembl__interpro__dm", "hsapiens_gene_ensembl__protein_feature_cdd__dm", 
          "hsapiens_gene_ensembl__protein_feature_gene3d__dm", 
          "hsapiens_gene_ensembl__protein_feature_hamap__dm", "hsapiens_gene_ensembl__protein_feature_hmmpanther__dm", 
          "hsapiens_gene_ensembl__protein_feature_pfam__dm", "hsapiens_gene_ensembl__protein_feature_pirsf__dm", 
          "hsapiens_gene_ensembl__protein_feature_prints__dm", 
          "hsapiens_gene_ensembl__protein_feature_scanprosite__dm", 
          "hsapiens_gene_ensembl__protein_feature_pfscan__dm", 
          "hsapiens_gene_ensembl__protein_feature_sfld__dm", "hsapiens_gene_ensembl__protein_feature_smart__dm", 
          "hsapiens_gene_ensembl__protein_feature_superfamily__dm", 
          "hsapiens_gene_ensembl__protein_feature_tigrfam__dm", 
          "hsapiens_gene_ensembl__mart_transcript_variation__dm", 
          "hsapiens_gene_ensembl__mart_transcript_variation__dm", 
          "pointer dataset"), filters9 = c("name_1059", "seq_region_end_1020", 
          "seq_region_start_1020", "seq_region_strand_1020", "name_1059,seq_region_end_1020,seq_region_start_1020,seq_region_strand_1020", 
          "ox_biogrid_bool", "ox_ccds_bool", "ox_chembl_bool", 
          "ox_dbass3_bool", "ox_dbass5_bool", "ox_ens_hs_transcript_bool", 
          "ox_ens_hs_translation_bool", "ox_entrezgene_trans_name_bool", 
          "ox_embl_bool", "ox_arrayexpress_bool", "ox_genedb_bool", 
          "ox_go_bool", "ox_goslim_goa_bool", "ox_hgnc_bool", "ox_hpa_bool", 
          "ox_protein_id_bool", "ox_ens_lrg_gene_bool", "ox_ens_lrg_transcript_bool", 
          "ox_merops_bool", "ox_mim_gene_bool", "ox_mim_morbid_bool", 
          "ox_mirbase_bool", "ox_mirbase_trans_name_bool", "ox_entrezgene_bool", 
          "ox_pdb_bool", "ox_reactome_bool", "ox_reactome_gene_bool", 
          "ox_reactome_transcript_bool", "ox_refseq_mrna_bool", 
          "ox_refseq_mrna_predicted_bool", "ox_refseq_ncrna_bool", 
          "ox_refseq_ncrna_predicted_bool", "ox_refseq_peptide_bool", 
          "ox_refseq_peptide_predicted_bool", "ox_rfam_bool", "ox_rfam_trans_name_bool", 
          "ox_rnacentral_bool", "ox_hgnc_trans_name_bool", "ox_ucsc_bool", 
          "ox_uniparc_bool", "ox_uniprot_gn_bool", "ox_uniprot_isoform_bool", 
          "ox_uniprotswissprot_bool", "ox_uniprotsptrembl_bool", 
          "ox_wikigene_bool", "stable_id_1023", "gene__main_stable_id_version", 
          "stable_id_1066", "transcript__main_stable_id_version", 
          "stable_id_1070", "translation__main_stable_id_version", 
          "stable_id_1016", "display_label_1074", "display_label_1074_r1", 
          "external_synonym", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "display_label_1074", "dbprimary_acc_1074", 
          "display_label_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "display_label_1074", 
          "display_label_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "display_label_1074", "dbprimary_acc_1074", "display_label_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "display_label_1074", 
          "dbprimary_acc_1074", "dbprimary_acc_1074", "dbprimary_acc_1074", 
          "dbprimary_acc_1074", "display_label_1074", "dbprimary_acc_1074", 
          "efg_affy_hc_g110_bool", "efg_affy_hg_focus_bool", "efg_affy_hg_u133a_bool", 
          "efg_affy_hg_u133a_2_bool", "efg_affy_hg_u133b_bool", 
          "efg_affy_hg_u133_plus_2_bool", "efg_affy_hg_u95a_bool", 
          "efg_affy_hg_u95av2_bool", "efg_affy_hg_u95b_bool", "efg_affy_hg_u95c_bool", 
          "efg_affy_hg_u95d_bool", "efg_affy_hg_u95e_bool", "efg_affy_hta_2_0_bool", 
          "efg_affy_huex_1_0_st_v2_bool", "efg_affy_hugenefl_bool", 
          "efg_affy_hugene_1_0_st_v1_bool", "efg_affy_hugene_2_0_st_v1_bool", 
          "efg_affy_hugene_2_1_st_v1_bool", "efg_affy_primeview_bool", 
          "efg_affy_u133_x3p_bool", "efg_agilent_cgh_44b_bool", 
          "efg_agilent_gpl26966_bool", "efg_agilent_gpl6848_bool", 
          "efg_agilent_sureprint_g3_ge_8x60k_bool", "efg_agilent_sureprint_g3_ge_8x60k_v2_bool", 
          "efg_agilent_wholegenome_bool", "efg_agilent_wholegenome_4x44k_v1_bool", 
          "efg_agilent_wholegenome_4x44k_v2_bool", "efg_codelink_codelink_bool", 
          "efg_illumina_humanht_12_v3_bool", "efg_illumina_humanht_12_v4_bool", 
          "efg_illumina_humanref_8_v3_bool", "efg_illumina_humanwg_6_v1_bool", 
          "efg_illumina_humanwg_6_v2_bool", "efg_illumina_humanwg_6_v3_bool", 
          "efg_phalanx_onearray_bool", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "display_label_11056", "display_label_11056", 
          "display_label_11056", "transcript_count", "transcript_count", 
          "biotype_1020", "biotype_1064", "source_1020", "source_1064", 
          "value_1065", "value_1065", "value_1065", "value_1065", 
          "value_1065", "value_1065", "description_20125", "source_20125", 
          "accession_305_r1", "name_305_r1", "linkage_type_1024", 
          "paralog_hsapiens_bool", "homolog_cabingdonii_bool", 
          "homolog_scaustralis_bool", "homolog_mspretus_bool", 
          "homolog_vpacos_bool", "homolog_mmmarmota_bool", "homolog_pformosa_bool", 
          "homolog_bbbison_bool", "homolog_uamericanus_bool", "homolog_nvison_bool", 
          "homolog_cdromedarius_bool", "homolog_uparryii_bool", 
          "homolog_smerianae_bool", "homolog_dnovemcinctus_bool", 
          "homolog_sformosus_bool", "homolog_gmorhua_bool", "homolog_charengus_bool", 
          "homolog_ssalar_bool", "homolog_cporosus_bool", "homolog_lbergylta_bool", 
          "homolog_lcalcarifer_bool", "homolog_dleucas_bool", "homolog_spartitus_bool", 
          "homolog_rbieti_bool", "homolog_bmusculus_bool", "homolog_llaticaudata_bool", 
          "homolog_sbboliviensis_bool", "homolog_ppaniscus_bool", 
          "homolog_strutta_bool", "homolog_hburtoni_bool", "homolog_ogarnettii_bool", 
          "homolog_cintestinalis_bool", "homolog_csavignyi_bool", 
          "homolog_celegans_bool", "homolog_ccapucinus_bool", "homolog_fcatus_bool", 
          "homolog_cwagneri_bool", "homolog_cgobio_bool", "homolog_ipunctatus_bool", 
          "homolog_ggallus_bool", "homolog_ptroglodytes_bool", 
          "homolog_cgchok1gshd_bool", "homolog_osinensis_bool", 
          "homolog_psinensis_bool", "homolog_otshawytscha_bool", 
          "homolog_atestudineus_bool", "homolog_aocellaris_bool", 
          "homolog_lchalumnae_bool", "homolog_okisutch_bool", "homolog_falbicollis_bool", 
          "homolog_scanaria_bool", "homolog_ccarpio_bool", "homolog_pmuralis_bool", 
          "homolog_vursinus_bool", "homolog_pcoquereli_bool", "homolog_btaurus_bool", 
          "homolog_mfascicularis_bool", "homolog_odegus_bool", 
          "homolog_dclupeoides_bool", "homolog_cldingo_bool", "homolog_clfamiliaris_bool", 
          "homolog_ttruncatus_bool", "homolog_bgrunniens_bool", 
          "homolog_eaasinus_bool", "homolog_mleucophaeus_bool", 
          "homolog_dmelanogaster_bool", "homolog_applatyrhynchos_bool", 
          "homolog_ptextilis_bool", "homolog_acalliptera_bool", 
          "homolog_eelectricus_bool", "homolog_lafricana_bool", 
          "homolog_cmilii_bool", "homolog_svulgaris_bool", "homolog_dlabrax_bool", 
          "homolog_mpfuro_bool", "homolog_trubripes_bool", "homolog_amelanoleuca_bool", 
          "homolog_nleucogenys_bool", "homolog_saurata_bool", "homolog_chircus_bool", 
          "homolog_mauratus_bool", "homolog_acchrysaetos_bool", 
          "homolog_rroxellana_bool", "homolog_sgrahami_bool", "homolog_cauratus_bool", 
          "homolog_gevgoodei_bool", "homolog_ggorilla_bool", "homolog_pmajor_bool", 
          "homolog_sdumerili_bool", "homolog_psimus_bool", "homolog_rferrumequinum_bool", 
          "homolog_acarolinensis_bool", "homolog_cporcellus_bool", 
          "homolog_preticulata_bool", "homolog_eburgeri_bool", 
          "homolog_eeuropaeus_bool", "homolog_ecaballus_bool", 
          "homolog_hhucho_bool", "homolog_bihybrid_bool", "homolog_pcapensis_bool", 
          "homolog_nnaja_bool", "homolog_omelastigma_bool", "homolog_olatipes_bool", 
          "homolog_cjaponica_bool", "homolog_ojavanicus_bool", 
          "homolog_shabroptila_bool", "homolog_dordii_bool", "homolog_pcinereus_bool", 
          "homolog_pmarinus_bool", "homolog_lcrocea_bool", "homolog_lleishanense_bool", 
          "homolog_ppardus_bool", "homolog_jjaculus_bool", "homolog_etelfairi_bool", 
          "homolog_pleo_bool", "homolog_clanigera_bool", "homolog_clumpus_bool", 
          "homolog_nbrichardi_bool", "homolog_anancymaae_bool", 
          "homolog_mmulatta_bool", "homolog_nscutatus_bool", "homolog_pnyererei_bool", 
          "homolog_kmarmoratus_bool", "homolog_gfortis_bool", "homolog_pvampyrus_bool", 
          "homolog_amexicanus_bool", "homolog_mlucifugus_bool", 
          "homolog_acitrinellus_bool", "homolog_mmusculus_bool", 
          "homolog_mmurinus_bool", "homolog_fheteroclitus_bool", 
          "homolog_hgfemale_bool", "homolog_mmonoceros_bool", "homolog_oniloticus_bool", 
          "homolog_pmbairdii_bool", "homolog_elucius_bool", "homolog_panubis_bool", 
          "homolog_mdomestica_bool", "homolog_apercula_bool", "homolog_cpbellii_bool", 
          "homolog_pkingsleyae_bool", "homolog_sscrofa_bool", "homolog_mnemestrina_bool", 
          "homolog_oprinceps_bool", "homolog_slucioperca_bool", 
          "homolog_mmurdjan_bool", "homolog_abrachyrhynchus_bool", 
          "homolog_xmaculatus_bool", "homolog_oanatinus_bool", 
          "homolog_umaritimus_bool", "homolog_mochrogaster_bool", 
          "homolog_ocuniculus_bool", "homolog_omykiss_bool", "homolog_rnorvegicus_bool", 
          "homolog_vvulpes_bool", "homolog_pnattereri_bool", "homolog_ecalabaricus_bool", 
          "homolog_mcaroli_bool", "homolog_scerevisiae_bool", "homolog_platipinna_bool", 
          "homolog_oarambouillet_bool", "homolog_cvariegatus_bool", 
          "homolog_saraneus_bool", "homolog_mpahari_bool", "homolog_bsplendens_bool", 
          "homolog_mmoschiferus_bool", "homolog_choffmanni_bool", 
          "homolog_catys_bool", "homolog_pcatodon_bool", "homolog_apolyacanthus_bool", 
          "homolog_loculatus_bool", "homolog_itridecemlineatus_bool", 
          "homolog_mspicilegus_bool", "homolog_gaculeatus_bool", 
          "homolog_pabelii_bool", "homolog_csyrichta_bool", "homolog_sharrisii_bool", 
          "homolog_tnigroviridis_bool", "homolog_tctriunguis_bool", 
          "homolog_ptaltaica_bool", "homolog_hcomes_bool", "homolog_csemilaevis_bool", 
          "homolog_tbelangeri_bool", "homolog_xtropicalis_bool", 
          "homolog_spunctatus_bool", "homolog_smaximus_bool", "homolog_mgallopavo_bool", 
          "homolog_nfurzeri_bool", "homolog_ngalili_bool", "homolog_psinus_bool", 
          "homolog_csabaeus_bool", "homolog_neugenii_bool", "homolog_cjacchus_bool", 
          "homolog_bmutus_bool", "homolog_chyarkandensis_bool", 
          "homolog_sldorsalis_bool", "homolog_tguttata_bool", "homolog_mzebra_bool", 
          "homolog_drerio_bool", "homolog_marmatus_bool", "interpro_bool", 
          "protein_feature_cdd_bool", "protein_feature_gene3d_bool", 
          "protein_feature_hamap_bool", "protein_feature_mobidblite_bool", 
          "protein_feature_ncoils_bool", "protein_feature_hmmpanther_bool", 
          "protein_feature_pfam_bool", "protein_feature_pirsf_bool", 
          "protein_feature_prints_bool", "protein_feature_scanprosite_bool", 
          "protein_feature_pfscan_bool", "protein_feature_seg_bool", 
          "protein_feature_sfld_bool", "protein_feature_sifts_import_bool", 
          "protein_feature_signalp_bool", "protein_feature_smart_bool", 
          "protein_feature_superfamily_bool", "protein_feature_tigrfam_bool", 
          "protein_feature_tmhmm_bool", "interpro_ac_1026", "hit_name_1048", 
          "hit_name_1048", "hit_name_1048", "hit_name_1048", "hit_name_1048", 
          "hit_name_1048", "hit_name_1048", "hit_name_1048", "hit_name_1048", 
          "hit_name_1048", "hit_name_1048", "hit_name_1048", "hit_name_1048", 
          "name_2021", "evidence_2025", "name_305_r1")), class = "data.frame", row.names = c(NA, 
          -439L)), attributes = structure(list(name = c("ensembl_gene_id", 
          "ensembl_gene_id_version", "ensembl_transcript_id", "ensembl_transcript_id_version", 
          "ensembl_peptide_id", "ensembl_peptide_id_version", "ensembl_exon_id", 
          "description", "chromosome_name", "start_position", "end_position", 
          "strand", "band", "transcript_start", "transcript_end", 
          "transcription_start_site", "transcript_length", "transcript_tsl", 
          "transcript_gencode_basic", "transcript_appris", "transcript_is_canonical", 
          "transcript_mane_select", "transcript_mane_plus_clinical", 
          "external_gene_name", "external_gene_source", "external_transcript_name", 
          "external_transcript_source_name", "transcript_count", 
          "percentage_gene_gc_content", "gene_biotype", "transcript_biotype", 
          "source", "transcript_source", "version", "transcript_version", 
          "peptide_version", "external_synonym", "phenotype_description", 
          "source_name", "study_external_id", "strain_name", "strain_gender", 
          "p_value", "go_id", "name_1006", "definition_1006", "go_linkage_type", 
          "namespace_1003", "goslim_goa_accession", "goslim_goa_description", 
          "biogrid", "ccds", "chembl", "dbass3_name", "dbass3_id", 
          "dbass5_name", "dbass5_id", "ens_hs_transcript", "ens_hs_translation", 
          "entrezgene_trans_name", "embl", "arrayexpress", "genedb", 
          "hgnc_id", "hgnc_symbol", "hpa_accession", "hpa_id", 
          "protein_id", "ens_lrg_gene", "ens_lrg_transcript", "merops", 
          "mim_gene_description", "mim_gene_accession", "mim_morbid_description", 
          "mim_morbid_accession", "mirbase_accession", "mirbase_id", 
          "mirbase_trans_name", "entrezgene_description", "entrezgene_accession", 
          "entrezgene_id", "pdb", "reactome", "reactome_gene", 
          "reactome_transcript", "refseq_mrna", "refseq_mrna_predicted", 
          "refseq_ncrna", "refseq_ncrna_predicted", "refseq_peptide", 
          "refseq_peptide_predicted", "rfam", "rfam_trans_name", 
          "rnacentral", "hgnc_trans_name", "ucsc", "uniparc", "uniprot_gn_symbol", 
          "uniprot_gn_id", "uniprot_isoform", "uniprotswissprot", 
          "uniprotsptrembl", "wikigene_description", "wikigene_name", 
          "wikigene_id", "affy_hc_g110", "affy_hg_focus", "affy_hg_u133a", 
          "affy_hg_u133a_2", "affy_hg_u133b", "affy_hg_u133_plus_2", 
          "affy_hg_u95a", "affy_hg_u95av2", "affy_hg_u95b", "affy_hg_u95c", 
          "affy_hg_u95d", "affy_hg_u95e", "affy_hta_2_0", "affy_huex_1_0_st_v2", 
          "affy_hugenefl", "affy_hugene_1_0_st_v1", "affy_hugene_2_0_st_v1", 
          "affy_hugene_2_1_st_v1", "affy_primeview", "affy_u133_x3p", 
          "agilent_cgh_44b", "agilent_gpl26966", "agilent_gpl6848", 
          "agilent_sureprint_g3_ge_8x60k", "agilent_sureprint_g3_ge_8x60k_v2", 
          "agilent_wholegenome", "agilent_wholegenome_4x44k_v1", 
          "agilent_wholegenome_4x44k_v2", "codelink_codelink", 
          "illumina_humanht_12_v3", "illumina_humanht_12_v4", "illumina_humanref_8_v3", 
          "illumina_humanwg_6_v1", "illumina_humanwg_6_v2", "illumina_humanwg_6_v3", 
          "phalanx_onearray", "cdd", "cdd_start", "cdd_end", "gene3d", 
          "gene3d_start", "gene3d_end", "hamap", "hamap_start", 
          "hamap_end", "hmmpanther", "hmmpanther_start", "hmmpanther_end", 
          "pfam", "pfam_start", "pfam_end", "pirsf", "pirsf_start", 
          "pirsf_end", "prints", "prints_start", "prints_end", 
          "scanprosite", "scanprosite_start", "scanprosite_end", 
          "pfscan", "pfscan_start", "pfscan_end", "sfld", "sfld_start", 
          "sfld_end", "smart", "smart_start", "smart_end", "superfamily", 
          "superfamily_start", "superfamily_end", "tigrfam", "tigrfam_start", 
          "tigrfam_end", "interpro", "interpro_short_description", 
          "interpro_description", "interpro_start", "interpro_end", 
          "mobidblite", "mobidblite_start", "mobidblite_end", "ncoils", 
          "ncoils_start", "ncoils_end", "seg", "seg_start", "seg_end", 
          "sifts_import", "sifts_import_start", "sifts_import_end", 
          "signalp", "signalp_start", "signalp_end", "tmhmm", "tmhmm_start", 
          "tmhmm_end", "ensembl_gene_id", "ensembl_gene_id_version", 
          "version", "ensembl_transcript_id", "ensembl_transcript_id_version", 
          "transcript_version", "ensembl_peptide_id", "ensembl_peptide_id_version", 
          "peptide_version", "chromosome_name", "start_position", 
          "end_position", "transcript_start", "transcript_end", 
          "transcription_start_site", "transcript_length", "strand", 
          "external_gene_name", "external_gene_source", "5_utr_start", 
          "5_utr_end", "3_utr_start", "3_utr_end", "cds_length", 
          "transcript_count", "description", "gene_biotype", "exon_chrom_start", 
          "exon_chrom_end", "is_constitutive", "rank", "phase", 
          "end_phase", "cdna_coding_start", "cdna_coding_end", 
          "genomic_coding_start", "genomic_coding_end", "ensembl_exon_id", 
          "cds_start", "cds_end", "ensembl_gene_id", "ensembl_gene_id_version", 
          "version", "ensembl_transcript_id", "ensembl_transcript_id_version", 
          "transcript_version", "ensembl_peptide_id", "ensembl_peptide_id_version", 
          "peptide_version", "chromosome_name", "start_position", 
          "end_position", "strand", "band", "external_gene_name", 
          "external_gene_source", "transcript_count", "percentage_gene_gc_content", 
          "description", "cabingdonii_homolog_ensembl_gene", "cabingdonii_homolog_associated_gene_name", 
          "cabingdonii_homolog_ensembl_peptide", "cabingdonii_homolog_chromosome", 
          "cabingdonii_homolog_chrom_start", "cabingdonii_homolog_chrom_end", 
          "cabingdonii_homolog_canonical_transcript_protein", "cabingdonii_homolog_subtype", 
          "cabingdonii_homolog_orthology_type", "cabingdonii_homolog_perc_id", 
          "cabingdonii_homolog_perc_id_r1", "cabingdonii_homolog_goc_score", 
          "cabingdonii_homolog_wga_coverage", "cabingdonii_homolog_orthology_confidence", 
          "scaustralis_homolog_ensembl_gene", "scaustralis_homolog_associated_gene_name", 
          "scaustralis_homolog_ensembl_peptide", "scaustralis_homolog_chromosome", 
          "scaustralis_homolog_chrom_start", "scaustralis_homolog_chrom_end", 
          "scaustralis_homolog_canonical_transcript_protein", "scaustralis_homolog_subtype", 
          "scaustralis_homolog_orthology_type", "scaustralis_homolog_perc_id", 
          "scaustralis_homolog_perc_id_r1", "scaustralis_homolog_goc_score", 
          "scaustralis_homolog_wga_coverage", "scaustralis_homolog_orthology_confidence", 
          "mspretus_homolog_ensembl_gene", "mspretus_homolog_associated_gene_name", 
          "mspretus_homolog_ensembl_peptide", "mspretus_homolog_chromosome", 
          "mspretus_homolog_chrom_start", "mspretus_homolog_chrom_end", 
          "mspretus_homolog_canonical_transcript_protein", "mspretus_homolog_subtype", 
          "mspretus_homolog_orthology_type", "mspretus_homolog_perc_id", 
          "mspretus_homolog_perc_id_r1", "mspretus_homolog_goc_score", 
          "mspretus_homolog_wga_coverage", "mspretus_homolog_orthology_confidence", 
          "vpacos_homolog_ensembl_gene", "vpacos_homolog_associated_gene_name", 
          "vpacos_homolog_ensembl_peptide", "vpacos_homolog_chromosome", 
          "vpacos_homolog_chrom_start", "vpacos_homolog_chrom_end", 
          "vpacos_homolog_canonical_transcript_protein", "vpacos_homolog_subtype", 
          "vpacos_homolog_orthology_type", "vpacos_homolog_perc_id", 
          "vpacos_homolog_perc_id_r1", "vpacos_homolog_goc_score", 
          "vpacos_homolog_wga_coverage", "vpacos_homolog_orthology_confidence", 
          "mmmarmota_homolog_ensembl_gene", "mmmarmota_homolog_associated_gene_name", 
          "mmmarmota_homolog_ensembl_peptide", "mmmarmota_homolog_chromosome", 
          "mmmarmota_homolog_chrom_start", "mmmarmota_homolog_chrom_end", 
          "mmmarmota_homolog_canonical_transcript_protein", "mmmarmota_homolog_subtype", 
          "mmmarmota_homolog_orthology_type", "mmmarmota_homolog_perc_id", 
          "mmmarmota_homolog_perc_id_r1", "mmmarmota_homolog_goc_score", 
          "mmmarmota_homolog_wga_coverage", "mmmarmota_homolog_orthology_confidence", 
          "pformosa_homolog_ensembl_gene", "pformosa_homolog_associated_gene_name", 
          "pformosa_homolog_ensembl_peptide", "pformosa_homolog_chromosome", 
          "pformosa_homolog_chrom_start", "pformosa_homolog_chrom_end", 
          "pformosa_homolog_canonical_transcript_protein", "pformosa_homolog_subtype", 
          "pformosa_homolog_orthology_type", "pformosa_homolog_perc_id", 
          "pformosa_homolog_perc_id_r1", "pformosa_homolog_goc_score", 
          "pformosa_homolog_wga_coverage", "pformosa_homolog_orthology_confidence", 
          "bbbison_homolog_ensembl_gene", "bbbison_homolog_associated_gene_name", 
          "bbbison_homolog_ensembl_peptide", "bbbison_homolog_chromosome", 
          "bbbison_homolog_chrom_start", "bbbison_homolog_chrom_end", 
          "bbbison_homolog_canonical_transcript_protein", "bbbison_homolog_subtype", 
          "bbbison_homolog_orthology_type", "bbbison_homolog_perc_id", 
          "bbbison_homolog_perc_id_r1", "bbbison_homolog_goc_score", 
          "bbbison_homolog_wga_coverage", "bbbison_homolog_orthology_confidence", 
          "uamericanus_homolog_ensembl_gene", "uamericanus_homolog_associated_gene_name", 
          "uamericanus_homolog_ensembl_peptide", "uamericanus_homolog_chromosome", 
          "uamericanus_homolog_chrom_start", "uamericanus_homolog_chrom_end", 
          "uamericanus_homolog_canonical_transcript_protein", "uamericanus_homolog_subtype", 
          "uamericanus_homolog_orthology_type", "uamericanus_homolog_perc_id", 
          "uamericanus_homolog_perc_id_r1", "uamericanus_homolog_goc_score", 
          "uamericanus_homolog_wga_coverage", "uamericanus_homolog_orthology_confidence", 
          "nvison_homolog_ensembl_gene", "nvison_homolog_associated_gene_name", 
          "nvison_homolog_ensembl_peptide", "nvison_homolog_chromosome", 
          "nvison_homolog_chrom_start", "nvison_homolog_chrom_end", 
          "nvison_homolog_canonical_transcript_protein", "nvison_homolog_subtype", 
          "nvison_homolog_orthology_type", "nvison_homolog_perc_id", 
          "nvison_homolog_perc_id_r1", "nvison_homolog_goc_score", 
          "nvison_homolog_wga_coverage", "nvison_homolog_orthology_confidence", 
          "cdromedarius_homolog_ensembl_gene", "cdromedarius_homolog_associated_gene_name", 
          "cdromedarius_homolog_ensembl_peptide", "cdromedarius_homolog_chromosome", 
          "cdromedarius_homolog_chrom_start", "cdromedarius_homolog_chrom_end", 
          "cdromedarius_homolog_canonical_transcript_protein", 
          "cdromedarius_homolog_subtype", "cdromedarius_homolog_orthology_type", 
          "cdromedarius_homolog_perc_id", "cdromedarius_homolog_perc_id_r1", 
          "cdromedarius_homolog_goc_score", "cdromedarius_homolog_wga_coverage", 
          "cdromedarius_homolog_orthology_confidence", "uparryii_homolog_ensembl_gene", 
          "uparryii_homolog_associated_gene_name", "uparryii_homolog_ensembl_peptide", 
          "uparryii_homolog_chromosome", "uparryii_homolog_chrom_start", 
          "uparryii_homolog_chrom_end", "uparryii_homolog_canonical_transcript_protein", 
          "uparryii_homolog_subtype", "uparryii_homolog_orthology_type", 
          "uparryii_homolog_perc_id", "uparryii_homolog_perc_id_r1", 
          "uparryii_homolog_goc_score", "uparryii_homolog_wga_coverage", 
          "uparryii_homolog_orthology_confidence", "smerianae_homolog_ensembl_gene", 
          "smerianae_homolog_associated_gene_name", "smerianae_homolog_ensembl_peptide", 
          "smerianae_homolog_chromosome", "smerianae_homolog_chrom_start", 
          "smerianae_homolog_chrom_end", "smerianae_homolog_canonical_transcript_protein", 
          "smerianae_homolog_subtype", "smerianae_homolog_orthology_type", 
          "smerianae_homolog_perc_id", "smerianae_homolog_perc_id_r1", 
          "smerianae_homolog_goc_score", "smerianae_homolog_wga_coverage", 
          "smerianae_homolog_orthology_confidence", "dnovemcinctus_homolog_ensembl_gene", 
          "dnovemcinctus_homolog_associated_gene_name", "dnovemcinctus_homolog_ensembl_peptide", 
          "dnovemcinctus_homolog_chromosome", "dnovemcinctus_homolog_chrom_start", 
          "dnovemcinctus_homolog_chrom_end", "dnovemcinctus_homolog_canonical_transcript_protein", 
          "dnovemcinctus_homolog_subtype", "dnovemcinctus_homolog_orthology_type", 
          "dnovemcinctus_homolog_perc_id", "dnovemcinctus_homolog_perc_id_r1", 
          "dnovemcinctus_homolog_goc_score", "dnovemcinctus_homolog_wga_coverage", 
          "dnovemcinctus_homolog_orthology_confidence", "sformosus_homolog_ensembl_gene", 
          "sformosus_homolog_associated_gene_name", "sformosus_homolog_ensembl_peptide", 
          "sformosus_homolog_chromosome", "sformosus_homolog_chrom_start", 
          "sformosus_homolog_chrom_end", "sformosus_homolog_canonical_transcript_protein", 
          "sformosus_homolog_subtype", "sformosus_homolog_orthology_type", 
          "sformosus_homolog_perc_id", "sformosus_homolog_perc_id_r1", 
          "sformosus_homolog_goc_score", "sformosus_homolog_wga_coverage", 
          "sformosus_homolog_orthology_confidence", "gmorhua_homolog_ensembl_gene", 
          "gmorhua_homolog_associated_gene_name", "gmorhua_homolog_ensembl_peptide", 
          "gmorhua_homolog_chromosome", "gmorhua_homolog_chrom_start", 
          "gmorhua_homolog_chrom_end", "gmorhua_homolog_canonical_transcript_protein", 
          "gmorhua_homolog_subtype", "gmorhua_homolog_orthology_type", 
          "gmorhua_homolog_perc_id", "gmorhua_homolog_perc_id_r1", 
          "gmorhua_homolog_goc_score", "gmorhua_homolog_orthology_confidence", 
          "charengus_homolog_ensembl_gene", "charengus_homolog_associated_gene_name", 
          "charengus_homolog_ensembl_peptide", "charengus_homolog_chromosome", 
          "charengus_homolog_chrom_start", "charengus_homolog_chrom_end", 
          "charengus_homolog_canonical_transcript_protein", "charengus_homolog_subtype", 
          "charengus_homolog_orthology_type", "charengus_homolog_perc_id", 
          "charengus_homolog_perc_id_r1", "charengus_homolog_goc_score", 
          "charengus_homolog_wga_coverage", "charengus_homolog_orthology_confidence", 
          "ssalar_homolog_ensembl_gene", "ssalar_homolog_associated_gene_name", 
          "ssalar_homolog_ensembl_peptide", "ssalar_homolog_chromosome", 
          "ssalar_homolog_chrom_start", "ssalar_homolog_chrom_end", 
          "ssalar_homolog_canonical_transcript_protein", "ssalar_homolog_subtype", 
          "ssalar_homolog_orthology_type", "ssalar_homolog_perc_id", 
          "ssalar_homolog_perc_id_r1", "ssalar_homolog_goc_score", 
          "ssalar_homolog_wga_coverage", "ssalar_homolog_orthology_confidence", 
          "cporosus_homolog_ensembl_gene", "cporosus_homolog_associated_gene_name", 
          "cporosus_homolog_ensembl_peptide", "cporosus_homolog_chromosome", 
          "cporosus_homolog_chrom_start", "cporosus_homolog_chrom_end", 
          "cporosus_homolog_canonical_transcript_protein", "cporosus_homolog_subtype", 
          "cporosus_homolog_orthology_type", "cporosus_homolog_perc_id", 
          "cporosus_homolog_perc_id_r1", "cporosus_homolog_goc_score", 
          "cporosus_homolog_wga_coverage", "cporosus_homolog_orthology_confidence", 
          "lbergylta_homolog_ensembl_gene", "lbergylta_homolog_associated_gene_name", 
          "lbergylta_homolog_ensembl_peptide", "lbergylta_homolog_chromosome", 
          "lbergylta_homolog_chrom_start", "lbergylta_homolog_chrom_end", 
          "lbergylta_homolog_canonical_transcript_protein", "lbergylta_homolog_subtype", 
          "lbergylta_homolog_orthology_type", "lbergylta_homolog_perc_id", 
          "lbergylta_homolog_perc_id_r1", "lbergylta_homolog_goc_score", 
          "lbergylta_homolog_wga_coverage", "lbergylta_homolog_orthology_confidence", 
          "lcalcarifer_homolog_ensembl_gene", "lcalcarifer_homolog_associated_gene_name", 
          "lcalcarifer_homolog_ensembl_peptide", "lcalcarifer_homolog_chromosome", 
          "lcalcarifer_homolog_chrom_start", "lcalcarifer_homolog_chrom_end", 
          "lcalcarifer_homolog_canonical_transcript_protein", "lcalcarifer_homolog_subtype", 
          "lcalcarifer_homolog_orthology_type", "lcalcarifer_homolog_perc_id", 
          "lcalcarifer_homolog_perc_id_r1", "lcalcarifer_homolog_goc_score", 
          "lcalcarifer_homolog_wga_coverage", "lcalcarifer_homolog_orthology_confidence", 
          "dleucas_homolog_ensembl_gene", "dleucas_homolog_associated_gene_name", 
          "dleucas_homolog_ensembl_peptide", "dleucas_homolog_chromosome", 
          "dleucas_homolog_chrom_start", "dleucas_homolog_chrom_end", 
          "dleucas_homolog_canonical_transcript_protein", "dleucas_homolog_subtype", 
          "dleucas_homolog_orthology_type", "dleucas_homolog_perc_id", 
          "dleucas_homolog_perc_id_r1", "dleucas_homolog_goc_score", 
          "dleucas_homolog_wga_coverage", "dleucas_homolog_orthology_confidence", 
          "spartitus_homolog_ensembl_gene", "spartitus_homolog_associated_gene_name", 
          "spartitus_homolog_ensembl_peptide", "spartitus_homolog_chromosome", 
          "spartitus_homolog_chrom_start", "spartitus_homolog_chrom_end", 
          "spartitus_homolog_canonical_transcript_protein", "spartitus_homolog_subtype", 
          "spartitus_homolog_orthology_type", "spartitus_homolog_perc_id", 
          "spartitus_homolog_perc_id_r1", "spartitus_homolog_goc_score", 
          "spartitus_homolog_wga_coverage", "spartitus_homolog_orthology_confidence", 
          "rbieti_homolog_ensembl_gene", "rbieti_homolog_associated_gene_name", 
          "rbieti_homolog_ensembl_peptide", "rbieti_homolog_chromosome", 
          "rbieti_homolog_chrom_start", "rbieti_homolog_chrom_end", 
          "rbieti_homolog_canonical_transcript_protein", "rbieti_homolog_subtype", 
          "rbieti_homolog_orthology_type", "rbieti_homolog_perc_id", 
          "rbieti_homolog_perc_id_r1", "rbieti_homolog_goc_score", 
          "rbieti_homolog_wga_coverage", "rbieti_homolog_orthology_confidence", 
          "bmusculus_homolog_ensembl_gene", "bmusculus_homolog_associated_gene_name", 
          "bmusculus_homolog_ensembl_peptide", "bmusculus_homolog_chromosome", 
          "bmusculus_homolog_chrom_start", "bmusculus_homolog_chrom_end", 
          "bmusculus_homolog_canonical_transcript_protein", "bmusculus_homolog_subtype", 
          "bmusculus_homolog_orthology_type", "bmusculus_homolog_perc_id", 
          "bmusculus_homolog_perc_id_r1", "bmusculus_homolog_goc_score", 
          "bmusculus_homolog_wga_coverage", "bmusculus_homolog_orthology_confidence", 
          "llaticaudata_homolog_ensembl_gene", "llaticaudata_homolog_associated_gene_name", 
          "llaticaudata_homolog_ensembl_peptide", "llaticaudata_homolog_chromosome", 
          "llaticaudata_homolog_chrom_start", "llaticaudata_homolog_chrom_end", 
          "llaticaudata_homolog_canonical_transcript_protein", 
          "llaticaudata_homolog_subtype", "llaticaudata_homolog_orthology_type", 
          "llaticaudata_homolog_perc_id", "llaticaudata_homolog_perc_id_r1", 
          "llaticaudata_homolog_goc_score", "llaticaudata_homolog_wga_coverage", 
          "llaticaudata_homolog_orthology_confidence", "sbboliviensis_homolog_ensembl_gene", 
          "sbboliviensis_homolog_associated_gene_name", "sbboliviensis_homolog_ensembl_peptide", 
          "sbboliviensis_homolog_chromosome", "sbboliviensis_homolog_chrom_start", 
          "sbboliviensis_homolog_chrom_end", "sbboliviensis_homolog_canonical_transcript_protein", 
          "sbboliviensis_homolog_subtype", "sbboliviensis_homolog_orthology_type", 
          "sbboliviensis_homolog_perc_id", "sbboliviensis_homolog_perc_id_r1", 
          "sbboliviensis_homolog_goc_score", "sbboliviensis_homolog_wga_coverage", 
          "sbboliviensis_homolog_orthology_confidence", "ppaniscus_homolog_ensembl_gene", 
          "ppaniscus_homolog_associated_gene_name", "ppaniscus_homolog_ensembl_peptide", 
          "ppaniscus_homolog_chromosome", "ppaniscus_homolog_chrom_start", 
          "ppaniscus_homolog_chrom_end", "ppaniscus_homolog_canonical_transcript_protein", 
          "ppaniscus_homolog_subtype", "ppaniscus_homolog_orthology_type", 
          "ppaniscus_homolog_perc_id", "ppaniscus_homolog_perc_id_r1", 
          "ppaniscus_homolog_goc_score", "ppaniscus_homolog_wga_coverage", 
          "ppaniscus_homolog_orthology_confidence", "strutta_homolog_ensembl_gene", 
          "strutta_homolog_associated_gene_name", "strutta_homolog_ensembl_peptide", 
          "strutta_homolog_chromosome", "strutta_homolog_chrom_start", 
          "strutta_homolog_chrom_end", "strutta_homolog_canonical_transcript_protein", 
          "strutta_homolog_subtype", "strutta_homolog_orthology_type", 
          "strutta_homolog_perc_id", "strutta_homolog_perc_id_r1", 
          "strutta_homolog_goc_score", "strutta_homolog_wga_coverage", 
          "strutta_homolog_orthology_confidence", "hburtoni_homolog_ensembl_gene", 
          "hburtoni_homolog_associated_gene_name", "hburtoni_homolog_ensembl_peptide", 
          "hburtoni_homolog_chromosome", "hburtoni_homolog_chrom_start", 
          "hburtoni_homolog_chrom_end", "hburtoni_homolog_canonical_transcript_protein", 
          "hburtoni_homolog_subtype", "hburtoni_homolog_orthology_type", 
          "hburtoni_homolog_perc_id", "hburtoni_homolog_perc_id_r1", 
          "hburtoni_homolog_goc_score", "hburtoni_homolog_wga_coverage", 
          "hburtoni_homolog_orthology_confidence", "ogarnettii_homolog_ensembl_gene", 
          "ogarnettii_homolog_associated_gene_name", "ogarnettii_homolog_ensembl_peptide", 
          "ogarnettii_homolog_chromosome", "ogarnettii_homolog_chrom_start", 
          "ogarnettii_homolog_chrom_end", "ogarnettii_homolog_canonical_transcript_protein", 
          "ogarnettii_homolog_subtype", "ogarnettii_homolog_orthology_type", 
          "ogarnettii_homolog_perc_id", "ogarnettii_homolog_perc_id_r1", 
          "ogarnettii_homolog_goc_score", "ogarnettii_homolog_wga_coverage", 
          "ogarnettii_homolog_orthology_confidence", "cintestinalis_homolog_ensembl_gene", 
          "cintestinalis_homolog_associated_gene_name", "cintestinalis_homolog_ensembl_peptide", 
          "cintestinalis_homolog_chromosome", "cintestinalis_homolog_chrom_start", 
          "cintestinalis_homolog_chrom_end", "cintestinalis_homolog_canonical_transcript_protein", 
          "cintestinalis_homolog_subtype", "cintestinalis_homolog_orthology_type", 
          "cintestinalis_homolog_perc_id", "cintestinalis_homolog_perc_id_r1", 
          "cintestinalis_homolog_wga_coverage", "cintestinalis_homolog_orthology_confidence", 
          "csavignyi_homolog_ensembl_gene", "csavignyi_homolog_associated_gene_name", 
          "csavignyi_homolog_ensembl_peptide", "csavignyi_homolog_chromosome", 
          "csavignyi_homolog_chrom_start", "csavignyi_homolog_chrom_end", 
          "csavignyi_homolog_canonical_transcript_protein", "csavignyi_homolog_subtype", 
          "csavignyi_homolog_orthology_type", "csavignyi_homolog_perc_id", 
          "csavignyi_homolog_perc_id_r1", "csavignyi_homolog_wga_coverage", 
          "csavignyi_homolog_orthology_confidence", "celegans_homolog_ensembl_gene", 
          "celegans_homolog_associated_gene_name", "celegans_homolog_ensembl_peptide", 
          "celegans_homolog_chromosome", "celegans_homolog_chrom_start", 
          "celegans_homolog_chrom_end", "celegans_homolog_canonical_transcript_protein", 
          "celegans_homolog_subtype", "celegans_homolog_orthology_type", 
          "celegans_homolog_perc_id", "celegans_homolog_perc_id_r1", 
          "celegans_homolog_orthology_confidence", "ccapucinus_homolog_ensembl_gene", 
          "ccapucinus_homolog_associated_gene_name", "ccapucinus_homolog_ensembl_peptide", 
          "ccapucinus_homolog_chromosome", "ccapucinus_homolog_chrom_start", 
          "ccapucinus_homolog_chrom_end", "ccapucinus_homolog_canonical_transcript_protein", 
          "ccapucinus_homolog_subtype", "ccapucinus_homolog_orthology_type", 
          "ccapucinus_homolog_perc_id", "ccapucinus_homolog_perc_id_r1", 
          "ccapucinus_homolog_goc_score", "ccapucinus_homolog_wga_coverage", 
          "ccapucinus_homolog_orthology_confidence", "fcatus_homolog_ensembl_gene", 
          "fcatus_homolog_associated_gene_name", "fcatus_homolog_ensembl_peptide", 
          "fcatus_homolog_chromosome", "fcatus_homolog_chrom_start", 
          "fcatus_homolog_chrom_end", "fcatus_homolog_canonical_transcript_protein", 
          "fcatus_homolog_subtype", "fcatus_homolog_orthology_type", 
          "fcatus_homolog_perc_id", "fcatus_homolog_perc_id_r1", 
          "fcatus_homolog_goc_score", "fcatus_homolog_wga_coverage", 
          "fcatus_homolog_orthology_confidence", "cwagneri_homolog_ensembl_gene", 
          "cwagneri_homolog_associated_gene_name", "cwagneri_homolog_ensembl_peptide", 
          "cwagneri_homolog_chromosome", "cwagneri_homolog_chrom_start", 
          "cwagneri_homolog_chrom_end", "cwagneri_homolog_canonical_transcript_protein", 
          "cwagneri_homolog_subtype", "cwagneri_homolog_orthology_type", 
          "cwagneri_homolog_perc_id", "cwagneri_homolog_perc_id_r1", 
          "cwagneri_homolog_goc_score", "cwagneri_homolog_wga_coverage", 
          "cwagneri_homolog_orthology_confidence", "cgobio_homolog_ensembl_gene", 
          "cgobio_homolog_associated_gene_name", "cgobio_homolog_ensembl_peptide", 
          "cgobio_homolog_chromosome", "cgobio_homolog_chrom_start", 
          "cgobio_homolog_chrom_end", "cgobio_homolog_canonical_transcript_protein", 
          "cgobio_homolog_subtype", "cgobio_homolog_orthology_type", 
          "cgobio_homolog_perc_id", "cgobio_homolog_perc_id_r1", 
          "cgobio_homolog_goc_score", "cgobio_homolog_wga_coverage", 
          "cgobio_homolog_orthology_confidence", "ipunctatus_homolog_ensembl_gene", 
          "ipunctatus_homolog_associated_gene_name", "ipunctatus_homolog_ensembl_peptide", 
          "ipunctatus_homolog_chromosome", "ipunctatus_homolog_chrom_start", 
          "ipunctatus_homolog_chrom_end", "ipunctatus_homolog_canonical_transcript_protein", 
          "ipunctatus_homolog_subtype", "ipunctatus_homolog_orthology_type", 
          "ipunctatus_homolog_perc_id", "ipunctatus_homolog_perc_id_r1", 
          "ipunctatus_homolog_goc_score", "ipunctatus_homolog_wga_coverage", 
          "ipunctatus_homolog_orthology_confidence", "ggallus_homolog_ensembl_gene", 
          "ggallus_homolog_associated_gene_name", "ggallus_homolog_ensembl_peptide", 
          "ggallus_homolog_chromosome", "ggallus_homolog_chrom_start", 
          "ggallus_homolog_chrom_end", "ggallus_homolog_canonical_transcript_protein", 
          "ggallus_homolog_subtype", "ggallus_homolog_orthology_type", 
          "ggallus_homolog_perc_id", "ggallus_homolog_perc_id_r1", 
          "ggallus_homolog_goc_score", "ggallus_homolog_wga_coverage", 
          "ggallus_homolog_orthology_confidence", "ptroglodytes_homolog_ensembl_gene", 
          "ptroglodytes_homolog_associated_gene_name", "ptroglodytes_homolog_ensembl_peptide", 
          "ptroglodytes_homolog_chromosome", "ptroglodytes_homolog_chrom_start", 
          "ptroglodytes_homolog_chrom_end", "ptroglodytes_homolog_canonical_transcript_protein", 
          "ptroglodytes_homolog_subtype", "ptroglodytes_homolog_orthology_type", 
          "ptroglodytes_homolog_perc_id", "ptroglodytes_homolog_perc_id_r1", 
          "ptroglodytes_homolog_goc_score", "ptroglodytes_homolog_wga_coverage", 
          "ptroglodytes_homolog_orthology_confidence", "cgchok1gshd_homolog_ensembl_gene", 
          "cgchok1gshd_homolog_associated_gene_name", "cgchok1gshd_homolog_ensembl_peptide", 
          "cgchok1gshd_homolog_chromosome", "cgchok1gshd_homolog_chrom_start", 
          "cgchok1gshd_homolog_chrom_end", "cgchok1gshd_homolog_canonical_transcript_protein", 
          "cgchok1gshd_homolog_subtype", "cgchok1gshd_homolog_orthology_type", 
          "cgchok1gshd_homolog_perc_id", "cgchok1gshd_homolog_perc_id_r1", 
          "cgchok1gshd_homolog_goc_score", "cgchok1gshd_homolog_wga_coverage", 
          "cgchok1gshd_homolog_orthology_confidence", "osinensis_homolog_ensembl_gene", 
          "osinensis_homolog_associated_gene_name", "osinensis_homolog_ensembl_peptide", 
          "osinensis_homolog_chromosome", "osinensis_homolog_chrom_start", 
          "osinensis_homolog_chrom_end", "osinensis_homolog_canonical_transcript_protein", 
          "osinensis_homolog_subtype", "osinensis_homolog_orthology_type", 
          "osinensis_homolog_perc_id", "osinensis_homolog_perc_id_r1", 
          "osinensis_homolog_goc_score", "osinensis_homolog_wga_coverage", 
          "osinensis_homolog_orthology_confidence", "psinensis_homolog_ensembl_gene", 
          "psinensis_homolog_associated_gene_name", "psinensis_homolog_ensembl_peptide", 
          "psinensis_homolog_chromosome", "psinensis_homolog_chrom_start", 
          "psinensis_homolog_chrom_end", "psinensis_homolog_canonical_transcript_protein", 
          "psinensis_homolog_subtype", "psinensis_homolog_orthology_type", 
          "psinensis_homolog_perc_id", "psinensis_homolog_perc_id_r1", 
          "psinensis_homolog_goc_score", "psinensis_homolog_wga_coverage", 
          "psinensis_homolog_orthology_confidence", "otshawytscha_homolog_ensembl_gene", 
          "otshawytscha_homolog_associated_gene_name", "otshawytscha_homolog_ensembl_peptide", 
          "otshawytscha_homolog_chromosome", "otshawytscha_homolog_chrom_start", 
          "otshawytscha_homolog_chrom_end", "otshawytscha_homolog_canonical_transcript_protein", 
          "otshawytscha_homolog_subtype", "otshawytscha_homolog_orthology_type", 
          "otshawytscha_homolog_perc_id", "otshawytscha_homolog_perc_id_r1", 
          "otshawytscha_homolog_goc_score", "otshawytscha_homolog_wga_coverage", 
          "otshawytscha_homolog_orthology_confidence", "atestudineus_homolog_ensembl_gene", 
          "atestudineus_homolog_associated_gene_name", "atestudineus_homolog_ensembl_peptide", 
          "atestudineus_homolog_chromosome", "atestudineus_homolog_chrom_start", 
          "atestudineus_homolog_chrom_end", "atestudineus_homolog_canonical_transcript_protein", 
          "atestudineus_homolog_subtype", "atestudineus_homolog_orthology_type", 
          "atestudineus_homolog_perc_id", "atestudineus_homolog_perc_id_r1", 
          "atestudineus_homolog_goc_score", "atestudineus_homolog_orthology_confidence", 
          "aocellaris_homolog_ensembl_gene", "aocellaris_homolog_associated_gene_name", 
          "aocellaris_homolog_ensembl_peptide", "aocellaris_homolog_chromosome", 
          "aocellaris_homolog_chrom_start", "aocellaris_homolog_chrom_end", 
          "aocellaris_homolog_canonical_transcript_protein", "aocellaris_homolog_subtype", 
          "aocellaris_homolog_orthology_type", "aocellaris_homolog_perc_id", 
          "aocellaris_homolog_perc_id_r1", "aocellaris_homolog_goc_score", 
          "aocellaris_homolog_wga_coverage", "aocellaris_homolog_orthology_confidence", 
          "lchalumnae_homolog_ensembl_gene", "lchalumnae_homolog_associated_gene_name", 
          "lchalumnae_homolog_ensembl_peptide", "lchalumnae_homolog_chromosome", 
          "lchalumnae_homolog_chrom_start", "lchalumnae_homolog_chrom_end", 
          "lchalumnae_homolog_canonical_transcript_protein", "lchalumnae_homolog_subtype", 
          "lchalumnae_homolog_orthology_type", "lchalumnae_homolog_perc_id", 
          "lchalumnae_homolog_perc_id_r1", "lchalumnae_homolog_goc_score", 
          "lchalumnae_homolog_wga_coverage", "lchalumnae_homolog_orthology_confidence", 
          "okisutch_homolog_ensembl_gene", "okisutch_homolog_associated_gene_name", 
          "okisutch_homolog_ensembl_peptide", "okisutch_homolog_chromosome", 
          "okisutch_homolog_chrom_start", "okisutch_homolog_chrom_end", 
          "okisutch_homolog_canonical_transcript_protein", "okisutch_homolog_subtype", 
          "okisutch_homolog_orthology_type", "okisutch_homolog_perc_id", 
          "okisutch_homolog_perc_id_r1", "okisutch_homolog_goc_score", 
          "okisutch_homolog_wga_coverage", "okisutch_homolog_orthology_confidence", 
          "falbicollis_homolog_ensembl_gene", "falbicollis_homolog_associated_gene_name", 
          "falbicollis_homolog_ensembl_peptide", "falbicollis_homolog_chromosome", 
          "falbicollis_homolog_chrom_start", "falbicollis_homolog_chrom_end", 
          "falbicollis_homolog_canonical_transcript_protein", "falbicollis_homolog_subtype", 
          "falbicollis_homolog_orthology_type", "falbicollis_homolog_perc_id", 
          "falbicollis_homolog_perc_id_r1", "falbicollis_homolog_goc_score", 
          "falbicollis_homolog_orthology_confidence", "scanaria_homolog_ensembl_gene", 
          "scanaria_homolog_associated_gene_name", "scanaria_homolog_ensembl_peptide", 
          "scanaria_homolog_chromosome", "scanaria_homolog_chrom_start", 
          "scanaria_homolog_chrom_end", "scanaria_homolog_canonical_transcript_protein", 
          "scanaria_homolog_subtype", "scanaria_homolog_orthology_type", 
          "scanaria_homolog_perc_id", "scanaria_homolog_perc_id_r1", 
          "scanaria_homolog_goc_score", "scanaria_homolog_wga_coverage", 
          "scanaria_homolog_orthology_confidence", "ccarpio_homolog_ensembl_gene", 
          "ccarpio_homolog_associated_gene_name", "ccarpio_homolog_ensembl_peptide", 
          "ccarpio_homolog_chromosome", "ccarpio_homolog_chrom_start", 
          "ccarpio_homolog_chrom_end", "ccarpio_homolog_canonical_transcript_protein", 
          "ccarpio_homolog_subtype", "ccarpio_homolog_orthology_type", 
          "ccarpio_homolog_perc_id", "ccarpio_homolog_perc_id_r1", 
          "ccarpio_homolog_goc_score", "ccarpio_homolog_wga_coverage", 
          "ccarpio_homolog_orthology_confidence", "pmuralis_homolog_ensembl_gene", 
          "pmuralis_homolog_associated_gene_name", "pmuralis_homolog_ensembl_peptide", 
          "pmuralis_homolog_chromosome", "pmuralis_homolog_chrom_start", 
          "pmuralis_homolog_chrom_end", "pmuralis_homolog_canonical_transcript_protein", 
          "pmuralis_homolog_subtype", "pmuralis_homolog_orthology_type", 
          "pmuralis_homolog_perc_id", "pmuralis_homolog_perc_id_r1", 
          "pmuralis_homolog_goc_score", "pmuralis_homolog_wga_coverage", 
          "pmuralis_homolog_orthology_confidence", "vursinus_homolog_ensembl_gene", 
          "vursinus_homolog_associated_gene_name", "vursinus_homolog_ensembl_peptide", 
          "vursinus_homolog_chromosome", "vursinus_homolog_chrom_start", 
          "vursinus_homolog_chrom_end", "vursinus_homolog_canonical_transcript_protein", 
          "vursinus_homolog_subtype", "vursinus_homolog_orthology_type", 
          "vursinus_homolog_perc_id", "vursinus_homolog_perc_id_r1", 
          "vursinus_homolog_goc_score", "vursinus_homolog_wga_coverage", 
          "vursinus_homolog_orthology_confidence", "pcoquereli_homolog_ensembl_gene", 
          "pcoquereli_homolog_associated_gene_name", "pcoquereli_homolog_ensembl_peptide", 
          "pcoquereli_homolog_chromosome", "pcoquereli_homolog_chrom_start", 
          "pcoquereli_homolog_chrom_end", "pcoquereli_homolog_canonical_transcript_protein", 
          "pcoquereli_homolog_subtype", "pcoquereli_homolog_orthology_type", 
          "pcoquereli_homolog_perc_id", "pcoquereli_homolog_perc_id_r1", 
          "pcoquereli_homolog_goc_score", "pcoquereli_homolog_wga_coverage", 
          "pcoquereli_homolog_orthology_confidence", "btaurus_homolog_ensembl_gene", 
          "btaurus_homolog_associated_gene_name", "btaurus_homolog_ensembl_peptide", 
          "btaurus_homolog_chromosome", "btaurus_homolog_chrom_start", 
          "btaurus_homolog_chrom_end", "btaurus_homolog_canonical_transcript_protein", 
          "btaurus_homolog_subtype", "btaurus_homolog_orthology_type", 
          "btaurus_homolog_perc_id", "btaurus_homolog_perc_id_r1", 
          "btaurus_homolog_goc_score", "btaurus_homolog_wga_coverage", 
          "btaurus_homolog_orthology_confidence", "mfascicularis_homolog_ensembl_gene", 
          "mfascicularis_homolog_associated_gene_name", "mfascicularis_homolog_ensembl_peptide", 
          "mfascicularis_homolog_chromosome", "mfascicularis_homolog_chrom_start", 
          "mfascicularis_homolog_chrom_end", "mfascicularis_homolog_canonical_transcript_protein", 
          "mfascicularis_homolog_subtype", "mfascicularis_homolog_orthology_type", 
          "mfascicularis_homolog_perc_id", "mfascicularis_homolog_perc_id_r1", 
          "mfascicularis_homolog_goc_score", "mfascicularis_homolog_wga_coverage", 
          "mfascicularis_homolog_orthology_confidence", "odegus_homolog_ensembl_gene", 
          "odegus_homolog_associated_gene_name", "odegus_homolog_ensembl_peptide", 
          "odegus_homolog_chromosome", "odegus_homolog_chrom_start", 
          "odegus_homolog_chrom_end", "odegus_homolog_canonical_transcript_protein", 
          "odegus_homolog_subtype", "odegus_homolog_orthology_type", 
          "odegus_homolog_perc_id", "odegus_homolog_perc_id_r1", 
          "odegus_homolog_goc_score", "odegus_homolog_wga_coverage", 
          "odegus_homolog_orthology_confidence", "dclupeoides_homolog_ensembl_gene", 
          "dclupeoides_homolog_associated_gene_name", "dclupeoides_homolog_ensembl_peptide", 
          "dclupeoides_homolog_chromosome", "dclupeoides_homolog_chrom_start", 
          "dclupeoides_homolog_chrom_end", "dclupeoides_homolog_canonical_transcript_protein", 
          "dclupeoides_homolog_subtype", "dclupeoides_homolog_orthology_type", 
          "dclupeoides_homolog_perc_id", "dclupeoides_homolog_perc_id_r1", 
          "dclupeoides_homolog_goc_score", "dclupeoides_homolog_wga_coverage", 
          "dclupeoides_homolog_orthology_confidence", "cldingo_homolog_ensembl_gene", 
          "cldingo_homolog_associated_gene_name", "cldingo_homolog_ensembl_peptide", 
          "cldingo_homolog_chromosome", "cldingo_homolog_chrom_start", 
          "cldingo_homolog_chrom_end", "cldingo_homolog_canonical_transcript_protein", 
          "cldingo_homolog_subtype", "cldingo_homolog_orthology_type", 
          "cldingo_homolog_perc_id", "cldingo_homolog_perc_id_r1", 
          "cldingo_homolog_goc_score", "cldingo_homolog_wga_coverage", 
          "cldingo_homolog_orthology_confidence", "clfamiliaris_homolog_ensembl_gene", 
          "clfamiliaris_homolog_associated_gene_name", "clfamiliaris_homolog_ensembl_peptide", 
          "clfamiliaris_homolog_chromosome", "clfamiliaris_homolog_chrom_start", 
          "clfamiliaris_homolog_chrom_end", "clfamiliaris_homolog_canonical_transcript_protein", 
          "clfamiliaris_homolog_subtype", "clfamiliaris_homolog_orthology_type", 
          "clfamiliaris_homolog_perc_id", "clfamiliaris_homolog_perc_id_r1", 
          "clfamiliaris_homolog_goc_score", "clfamiliaris_homolog_wga_coverage", 
          "clfamiliaris_homolog_orthology_confidence", "ttruncatus_homolog_ensembl_gene", 
          "ttruncatus_homolog_associated_gene_name", "ttruncatus_homolog_ensembl_peptide", 
          "ttruncatus_homolog_chromosome", "ttruncatus_homolog_chrom_start", 
          "ttruncatus_homolog_chrom_end", "ttruncatus_homolog_canonical_transcript_protein", 
          "ttruncatus_homolog_subtype", "ttruncatus_homolog_orthology_type", 
          "ttruncatus_homolog_perc_id", "ttruncatus_homolog_perc_id_r1", 
          "ttruncatus_homolog_goc_score", "ttruncatus_homolog_wga_coverage", 
          "ttruncatus_homolog_orthology_confidence", "bgrunniens_homolog_ensembl_gene", 
          "bgrunniens_homolog_associated_gene_name", "bgrunniens_homolog_ensembl_peptide", 
          "bgrunniens_homolog_chromosome", "bgrunniens_homolog_chrom_start", 
          "bgrunniens_homolog_chrom_end", "bgrunniens_homolog_canonical_transcript_protein", 
          "bgrunniens_homolog_subtype", "bgrunniens_homolog_orthology_type", 
          "bgrunniens_homolog_perc_id", "bgrunniens_homolog_perc_id_r1", 
          "bgrunniens_homolog_goc_score", "bgrunniens_homolog_wga_coverage", 
          "bgrunniens_homolog_orthology_confidence", "eaasinus_homolog_ensembl_gene", 
          "eaasinus_homolog_associated_gene_name", "eaasinus_homolog_ensembl_peptide", 
          "eaasinus_homolog_chromosome", "eaasinus_homolog_chrom_start", 
          "eaasinus_homolog_chrom_end", "eaasinus_homolog_canonical_transcript_protein", 
          "eaasinus_homolog_subtype", "eaasinus_homolog_orthology_type", 
          "eaasinus_homolog_perc_id", "eaasinus_homolog_perc_id_r1", 
          "eaasinus_homolog_goc_score", "eaasinus_homolog_wga_coverage", 
          "eaasinus_homolog_orthology_confidence", "mleucophaeus_homolog_ensembl_gene", 
          "mleucophaeus_homolog_associated_gene_name", "mleucophaeus_homolog_ensembl_peptide", 
          "mleucophaeus_homolog_chromosome", "mleucophaeus_homolog_chrom_start", 
          "mleucophaeus_homolog_chrom_end", "mleucophaeus_homolog_canonical_transcript_protein", 
          "mleucophaeus_homolog_subtype", "mleucophaeus_homolog_orthology_type", 
          "mleucophaeus_homolog_perc_id", "mleucophaeus_homolog_perc_id_r1", 
          "mleucophaeus_homolog_goc_score", "mleucophaeus_homolog_wga_coverage", 
          "mleucophaeus_homolog_orthology_confidence", "dmelanogaster_homolog_ensembl_gene", 
          "dmelanogaster_homolog_associated_gene_name", "dmelanogaster_homolog_ensembl_peptide", 
          "dmelanogaster_homolog_chromosome", "dmelanogaster_homolog_chrom_start", 
          "dmelanogaster_homolog_chrom_end", "dmelanogaster_homolog_canonical_transcript_protein", 
          "dmelanogaster_homolog_subtype", "dmelanogaster_homolog_orthology_type", 
          "dmelanogaster_homolog_perc_id", "dmelanogaster_homolog_perc_id_r1", 
          "dmelanogaster_homolog_orthology_confidence", "applatyrhynchos_homolog_ensembl_gene", 
          "applatyrhynchos_homolog_associated_gene_name", "applatyrhynchos_homolog_ensembl_peptide", 
          "applatyrhynchos_homolog_chromosome", "applatyrhynchos_homolog_chrom_start", 
          "applatyrhynchos_homolog_chrom_end", "applatyrhynchos_homolog_canonical_transcript_protein", 
          "applatyrhynchos_homolog_subtype", "applatyrhynchos_homolog_orthology_type", 
          "applatyrhynchos_homolog_perc_id", "applatyrhynchos_homolog_perc_id_r1", 
          "applatyrhynchos_homolog_goc_score", "applatyrhynchos_homolog_wga_coverage", 
          "applatyrhynchos_homolog_orthology_confidence", "ptextilis_homolog_ensembl_gene", 
          "ptextilis_homolog_associated_gene_name", "ptextilis_homolog_ensembl_peptide", 
          "ptextilis_homolog_chromosome", "ptextilis_homolog_chrom_start", 
          "ptextilis_homolog_chrom_end", "ptextilis_homolog_canonical_transcript_protein", 
          "ptextilis_homolog_subtype", "ptextilis_homolog_orthology_type", 
          "ptextilis_homolog_perc_id", "ptextilis_homolog_perc_id_r1", 
          "ptextilis_homolog_goc_score", "ptextilis_homolog_wga_coverage", 
          "ptextilis_homolog_orthology_confidence", "acalliptera_homolog_ensembl_gene", 
          "acalliptera_homolog_associated_gene_name", "acalliptera_homolog_ensembl_peptide", 
          "acalliptera_homolog_chromosome", "acalliptera_homolog_chrom_start", 
          "acalliptera_homolog_chrom_end", "acalliptera_homolog_canonical_transcript_protein", 
          "acalliptera_homolog_subtype", "acalliptera_homolog_orthology_type", 
          "acalliptera_homolog_perc_id", "acalliptera_homolog_perc_id_r1", 
          "acalliptera_homolog_goc_score", "acalliptera_homolog_wga_coverage", 
          "acalliptera_homolog_orthology_confidence", "eelectricus_homolog_ensembl_gene", 
          "eelectricus_homolog_associated_gene_name", "eelectricus_homolog_ensembl_peptide", 
          "eelectricus_homolog_chromosome", "eelectricus_homolog_chrom_start", 
          "eelectricus_homolog_chrom_end", "eelectricus_homolog_canonical_transcript_protein", 
          "eelectricus_homolog_subtype", "eelectricus_homolog_orthology_type", 
          "eelectricus_homolog_perc_id", "eelectricus_homolog_perc_id_r1", 
          "eelectricus_homolog_goc_score", "eelectricus_homolog_wga_coverage", 
          "eelectricus_homolog_orthology_confidence", "lafricana_homolog_ensembl_gene", 
          "lafricana_homolog_associated_gene_name", "lafricana_homolog_ensembl_peptide", 
          "lafricana_homolog_chromosome", "lafricana_homolog_chrom_start", 
          "lafricana_homolog_chrom_end", "lafricana_homolog_canonical_transcript_protein", 
          "lafricana_homolog_subtype", "lafricana_homolog_orthology_type", 
          "lafricana_homolog_perc_id", "lafricana_homolog_perc_id_r1", 
          "lafricana_homolog_goc_score", "lafricana_homolog_wga_coverage", 
          "lafricana_homolog_orthology_confidence", "cmilii_homolog_ensembl_gene", 
          "cmilii_homolog_associated_gene_name", "cmilii_homolog_ensembl_peptide", 
          "cmilii_homolog_chromosome", "cmilii_homolog_chrom_start", 
          "cmilii_homolog_chrom_end", "cmilii_homolog_canonical_transcript_protein", 
          "cmilii_homolog_subtype", "cmilii_homolog_orthology_type", 
          "cmilii_homolog_perc_id", "cmilii_homolog_perc_id_r1", 
          "cmilii_homolog_wga_coverage", "cmilii_homolog_orthology_confidence", 
          "svulgaris_homolog_ensembl_gene", "svulgaris_homolog_associated_gene_name", 
          "svulgaris_homolog_ensembl_peptide", "svulgaris_homolog_chromosome", 
          "svulgaris_homolog_chrom_start", "svulgaris_homolog_chrom_end", 
          "svulgaris_homolog_canonical_transcript_protein", "svulgaris_homolog_subtype", 
          "svulgaris_homolog_orthology_type", "svulgaris_homolog_perc_id", 
          "svulgaris_homolog_perc_id_r1", "svulgaris_homolog_goc_score", 
          "svulgaris_homolog_wga_coverage", "svulgaris_homolog_orthology_confidence", 
          "dlabrax_homolog_ensembl_gene", "dlabrax_homolog_associated_gene_name", 
          "dlabrax_homolog_ensembl_peptide", "dlabrax_homolog_chromosome", 
          "dlabrax_homolog_chrom_start", "dlabrax_homolog_chrom_end", 
          "dlabrax_homolog_canonical_transcript_protein", "dlabrax_homolog_subtype", 
          "dlabrax_homolog_orthology_type", "dlabrax_homolog_perc_id", 
          "dlabrax_homolog_perc_id_r1", "dlabrax_homolog_goc_score", 
          "dlabrax_homolog_wga_coverage", "dlabrax_homolog_orthology_confidence", 
          "mpfuro_homolog_ensembl_gene", "mpfuro_homolog_associated_gene_name", 
          "mpfuro_homolog_ensembl_peptide", "mpfuro_homolog_chromosome", 
          "mpfuro_homolog_chrom_start", "mpfuro_homolog_chrom_end", 
          "mpfuro_homolog_canonical_transcript_protein", "mpfuro_homolog_subtype", 
          "mpfuro_homolog_orthology_type", "mpfuro_homolog_perc_id", 
          "mpfuro_homolog_perc_id_r1", "mpfuro_homolog_goc_score", 
          "mpfuro_homolog_wga_coverage", "mpfuro_homolog_orthology_confidence", 
          "trubripes_homolog_ensembl_gene", "trubripes_homolog_associated_gene_name", 
          "trubripes_homolog_ensembl_peptide", "trubripes_homolog_chromosome", 
          "trubripes_homolog_chrom_start", "trubripes_homolog_chrom_end", 
          "trubripes_homolog_canonical_transcript_protein", "trubripes_homolog_subtype", 
          "trubripes_homolog_orthology_type", "trubripes_homolog_perc_id", 
          "trubripes_homolog_perc_id_r1", "trubripes_homolog_goc_score", 
          "trubripes_homolog_wga_coverage", "trubripes_homolog_orthology_confidence", 
          "amelanoleuca_homolog_ensembl_gene", "amelanoleuca_homolog_associated_gene_name", 
          "amelanoleuca_homolog_ensembl_peptide", "amelanoleuca_homolog_chromosome", 
          "amelanoleuca_homolog_chrom_start", "amelanoleuca_homolog_chrom_end", 
          "amelanoleuca_homolog_canonical_transcript_protein", 
          "amelanoleuca_homolog_subtype", "amelanoleuca_homolog_orthology_type", 
          "amelanoleuca_homolog_perc_id", "amelanoleuca_homolog_perc_id_r1", 
          "amelanoleuca_homolog_goc_score", "amelanoleuca_homolog_orthology_confidence", 
          "nleucogenys_homolog_ensembl_gene", "nleucogenys_homolog_associated_gene_name", 
          "nleucogenys_homolog_ensembl_peptide", "nleucogenys_homolog_chromosome", 
          "nleucogenys_homolog_chrom_start", "nleucogenys_homolog_chrom_end", 
          "nleucogenys_homolog_canonical_transcript_protein", "nleucogenys_homolog_subtype", 
          "nleucogenys_homolog_orthology_type", "nleucogenys_homolog_perc_id", 
          "nleucogenys_homolog_perc_id_r1", "nleucogenys_homolog_goc_score", 
          "nleucogenys_homolog_wga_coverage", "nleucogenys_homolog_orthology_confidence", 
          "saurata_homolog_ensembl_gene", "saurata_homolog_associated_gene_name", 
          "saurata_homolog_ensembl_peptide", "saurata_homolog_chromosome", 
          "saurata_homolog_chrom_start", "saurata_homolog_chrom_end", 
          "saurata_homolog_canonical_transcript_protein", "saurata_homolog_subtype", 
          "saurata_homolog_orthology_type", "saurata_homolog_perc_id", 
          "saurata_homolog_perc_id_r1", "saurata_homolog_goc_score", 
          "saurata_homolog_wga_coverage", "saurata_homolog_orthology_confidence", 
          "chircus_homolog_ensembl_gene", "chircus_homolog_associated_gene_name", 
          "chircus_homolog_ensembl_peptide", "chircus_homolog_chromosome", 
          "chircus_homolog_chrom_start", "chircus_homolog_chrom_end", 
          "chircus_homolog_canonical_transcript_protein", "chircus_homolog_subtype", 
          "chircus_homolog_orthology_type", "chircus_homolog_perc_id", 
          "chircus_homolog_perc_id_r1", "chircus_homolog_goc_score", 
          "chircus_homolog_wga_coverage", "chircus_homolog_orthology_confidence", 
          "mauratus_homolog_ensembl_gene", "mauratus_homolog_associated_gene_name", 
          "mauratus_homolog_ensembl_peptide", "mauratus_homolog_chromosome", 
          "mauratus_homolog_chrom_start", "mauratus_homolog_chrom_end", 
          "mauratus_homolog_canonical_transcript_protein", "mauratus_homolog_subtype", 
          "mauratus_homolog_orthology_type", "mauratus_homolog_perc_id", 
          "mauratus_homolog_perc_id_r1", "mauratus_homolog_goc_score", 
          "mauratus_homolog_wga_coverage", "mauratus_homolog_orthology_confidence", 
          "acchrysaetos_homolog_ensembl_gene", "acchrysaetos_homolog_associated_gene_name", 
          "acchrysaetos_homolog_ensembl_peptide", "acchrysaetos_homolog_chromosome", 
          "acchrysaetos_homolog_chrom_start", "acchrysaetos_homolog_chrom_end", 
          "acchrysaetos_homolog_canonical_transcript_protein", 
          "acchrysaetos_homolog_subtype", "acchrysaetos_homolog_orthology_type", 
          "acchrysaetos_homolog_perc_id", "acchrysaetos_homolog_perc_id_r1", 
          "acchrysaetos_homolog_goc_score", "acchrysaetos_homolog_wga_coverage", 
          "acchrysaetos_homolog_orthology_confidence", "rroxellana_homolog_ensembl_gene", 
          "rroxellana_homolog_associated_gene_name", "rroxellana_homolog_ensembl_peptide", 
          "rroxellana_homolog_chromosome", "rroxellana_homolog_chrom_start", 
          "rroxellana_homolog_chrom_end", "rroxellana_homolog_canonical_transcript_protein", 
          "rroxellana_homolog_subtype", "rroxellana_homolog_orthology_type", 
          "rroxellana_homolog_perc_id", "rroxellana_homolog_perc_id_r1", 
          "rroxellana_homolog_goc_score", "rroxellana_homolog_wga_coverage", 
          "rroxellana_homolog_orthology_confidence", "sgrahami_homolog_ensembl_gene", 
          "sgrahami_homolog_associated_gene_name", "sgrahami_homolog_ensembl_peptide", 
          "sgrahami_homolog_chromosome", "sgrahami_homolog_chrom_start", 
          "sgrahami_homolog_chrom_end", "sgrahami_homolog_canonical_transcript_protein", 
          "sgrahami_homolog_subtype", "sgrahami_homolog_orthology_type", 
          "sgrahami_homolog_perc_id", "sgrahami_homolog_perc_id_r1", 
          "sgrahami_homolog_goc_score", "sgrahami_homolog_wga_coverage", 
          "sgrahami_homolog_orthology_confidence", "cauratus_homolog_ensembl_gene", 
          "cauratus_homolog_associated_gene_name", "cauratus_homolog_ensembl_peptide", 
          "cauratus_homolog_chromosome", "cauratus_homolog_chrom_start", 
          "cauratus_homolog_chrom_end", "cauratus_homolog_canonical_transcript_protein", 
          "cauratus_homolog_subtype", "cauratus_homolog_orthology_type", 
          "cauratus_homolog_perc_id", "cauratus_homolog_perc_id_r1", 
          "cauratus_homolog_goc_score", "cauratus_homolog_wga_coverage", 
          "cauratus_homolog_orthology_confidence", "gevgoodei_homolog_ensembl_gene", 
          "gevgoodei_homolog_associated_gene_name", "gevgoodei_homolog_ensembl_peptide", 
          "gevgoodei_homolog_chromosome", "gevgoodei_homolog_chrom_start", 
          "gevgoodei_homolog_chrom_end", "gevgoodei_homolog_canonical_transcript_protein", 
          "gevgoodei_homolog_subtype", "gevgoodei_homolog_orthology_type", 
          "gevgoodei_homolog_perc_id", "gevgoodei_homolog_perc_id_r1", 
          "gevgoodei_homolog_goc_score", "gevgoodei_homolog_wga_coverage", 
          "gevgoodei_homolog_orthology_confidence", "ggorilla_homolog_ensembl_gene", 
          "ggorilla_homolog_associated_gene_name", "ggorilla_homolog_ensembl_peptide", 
          "ggorilla_homolog_chromosome", "ggorilla_homolog_chrom_start", 
          "ggorilla_homolog_chrom_end", "ggorilla_homolog_canonical_transcript_protein", 
          "ggorilla_homolog_subtype", "ggorilla_homolog_orthology_type", 
          "ggorilla_homolog_perc_id", "ggorilla_homolog_perc_id_r1", 
          "ggorilla_homolog_goc_score", "ggorilla_homolog_wga_coverage", 
          "ggorilla_homolog_orthology_confidence", "pmajor_homolog_ensembl_gene", 
          "pmajor_homolog_associated_gene_name", "pmajor_homolog_ensembl_peptide", 
          "pmajor_homolog_chromosome", "pmajor_homolog_chrom_start", 
          "pmajor_homolog_chrom_end", "pmajor_homolog_canonical_transcript_protein", 
          "pmajor_homolog_subtype", "pmajor_homolog_orthology_type", 
          "pmajor_homolog_perc_id", "pmajor_homolog_perc_id_r1", 
          "pmajor_homolog_goc_score", "pmajor_homolog_wga_coverage", 
          "pmajor_homolog_orthology_confidence", "sdumerili_homolog_ensembl_gene", 
          "sdumerili_homolog_associated_gene_name", "sdumerili_homolog_ensembl_peptide", 
          "sdumerili_homolog_chromosome", "sdumerili_homolog_chrom_start", 
          "sdumerili_homolog_chrom_end", "sdumerili_homolog_canonical_transcript_protein", 
          "sdumerili_homolog_subtype", "sdumerili_homolog_orthology_type", 
          "sdumerili_homolog_perc_id", "sdumerili_homolog_perc_id_r1", 
          "sdumerili_homolog_goc_score", "sdumerili_homolog_wga_coverage", 
          "sdumerili_homolog_orthology_confidence", "psimus_homolog_ensembl_gene", 
          "psimus_homolog_associated_gene_name", "psimus_homolog_ensembl_peptide", 
          "psimus_homolog_chromosome", "psimus_homolog_chrom_start", 
          "psimus_homolog_chrom_end", "psimus_homolog_canonical_transcript_protein", 
          "psimus_homolog_subtype", "psimus_homolog_orthology_type", 
          "psimus_homolog_perc_id", "psimus_homolog_perc_id_r1", 
          "psimus_homolog_goc_score", "psimus_homolog_wga_coverage", 
          "psimus_homolog_orthology_confidence", "rferrumequinum_homolog_ensembl_gene", 
          "rferrumequinum_homolog_associated_gene_name", "rferrumequinum_homolog_ensembl_peptide", 
          "rferrumequinum_homolog_chromosome", "rferrumequinum_homolog_chrom_start", 
          "rferrumequinum_homolog_chrom_end", "rferrumequinum_homolog_canonical_transcript_protein", 
          "rferrumequinum_homolog_subtype", "rferrumequinum_homolog_orthology_type", 
          "rferrumequinum_homolog_perc_id", "rferrumequinum_homolog_perc_id_r1", 
          "rferrumequinum_homolog_goc_score", "rferrumequinum_homolog_wga_coverage", 
          "rferrumequinum_homolog_orthology_confidence", "acarolinensis_homolog_ensembl_gene", 
          "acarolinensis_homolog_associated_gene_name", "acarolinensis_homolog_ensembl_peptide", 
          "acarolinensis_homolog_chromosome", "acarolinensis_homolog_chrom_start", 
          "acarolinensis_homolog_chrom_end", "acarolinensis_homolog_canonical_transcript_protein", 
          "acarolinensis_homolog_subtype", "acarolinensis_homolog_orthology_type", 
          "acarolinensis_homolog_perc_id", "acarolinensis_homolog_perc_id_r1", 
          "acarolinensis_homolog_goc_score", "acarolinensis_homolog_orthology_confidence", 
          "cporcellus_homolog_ensembl_gene", "cporcellus_homolog_associated_gene_name", 
          "cporcellus_homolog_ensembl_peptide", "cporcellus_homolog_chromosome", 
          "cporcellus_homolog_chrom_start", "cporcellus_homolog_chrom_end", 
          "cporcellus_homolog_canonical_transcript_protein", "cporcellus_homolog_subtype", 
          "cporcellus_homolog_orthology_type", "cporcellus_homolog_perc_id", 
          "cporcellus_homolog_perc_id_r1", "cporcellus_homolog_goc_score", 
          "cporcellus_homolog_wga_coverage", "cporcellus_homolog_orthology_confidence", 
          "preticulata_homolog_ensembl_gene", "preticulata_homolog_associated_gene_name", 
          "preticulata_homolog_ensembl_peptide", "preticulata_homolog_chromosome", 
          "preticulata_homolog_chrom_start", "preticulata_homolog_chrom_end", 
          "preticulata_homolog_canonical_transcript_protein", "preticulata_homolog_subtype", 
          "preticulata_homolog_orthology_type", "preticulata_homolog_perc_id", 
          "preticulata_homolog_perc_id_r1", "preticulata_homolog_goc_score", 
          "preticulata_homolog_wga_coverage", "preticulata_homolog_orthology_confidence", 
          "eburgeri_homolog_ensembl_gene", "eburgeri_homolog_associated_gene_name", 
          "eburgeri_homolog_ensembl_peptide", "eburgeri_homolog_chromosome", 
          "eburgeri_homolog_chrom_start", "eburgeri_homolog_chrom_end", 
          "eburgeri_homolog_canonical_transcript_protein", "eburgeri_homolog_subtype", 
          "eburgeri_homolog_orthology_type", "eburgeri_homolog_perc_id", 
          "eburgeri_homolog_perc_id_r1", "eburgeri_homolog_wga_coverage", 
          "eburgeri_homolog_orthology_confidence", "eeuropaeus_homolog_ensembl_gene", 
          "eeuropaeus_homolog_associated_gene_name", "eeuropaeus_homolog_ensembl_peptide", 
          "eeuropaeus_homolog_chromosome", "eeuropaeus_homolog_chrom_start", 
          "eeuropaeus_homolog_chrom_end", "eeuropaeus_homolog_canonical_transcript_protein", 
          "eeuropaeus_homolog_subtype", "eeuropaeus_homolog_orthology_type", 
          "eeuropaeus_homolog_perc_id", "eeuropaeus_homolog_perc_id_r1", 
          "eeuropaeus_homolog_goc_score", "eeuropaeus_homolog_wga_coverage", 
          "eeuropaeus_homolog_orthology_confidence", "ecaballus_homolog_ensembl_gene", 
          "ecaballus_homolog_associated_gene_name", "ecaballus_homolog_ensembl_peptide", 
          "ecaballus_homolog_chromosome", "ecaballus_homolog_chrom_start", 
          "ecaballus_homolog_chrom_end", "ecaballus_homolog_canonical_transcript_protein", 
          "ecaballus_homolog_subtype", "ecaballus_homolog_orthology_type", 
          "ecaballus_homolog_perc_id", "ecaballus_homolog_perc_id_r1", 
          "ecaballus_homolog_goc_score", "ecaballus_homolog_wga_coverage", 
          "ecaballus_homolog_orthology_confidence", "hhucho_homolog_ensembl_gene", 
          "hhucho_homolog_associated_gene_name", "hhucho_homolog_ensembl_peptide", 
          "hhucho_homolog_chromosome", "hhucho_homolog_chrom_start", 
          "hhucho_homolog_chrom_end", "hhucho_homolog_canonical_transcript_protein", 
          "hhucho_homolog_subtype", "hhucho_homolog_orthology_type", 
          "hhucho_homolog_perc_id", "hhucho_homolog_perc_id_r1", 
          "hhucho_homolog_goc_score", "hhucho_homolog_wga_coverage", 
          "hhucho_homolog_orthology_confidence", "bihybrid_homolog_ensembl_gene", 
          "bihybrid_homolog_associated_gene_name", "bihybrid_homolog_ensembl_peptide", 
          "bihybrid_homolog_chromosome", "bihybrid_homolog_chrom_start", 
          "bihybrid_homolog_chrom_end", "bihybrid_homolog_canonical_transcript_protein", 
          "bihybrid_homolog_subtype", "bihybrid_homolog_orthology_type", 
          "bihybrid_homolog_perc_id", "bihybrid_homolog_perc_id_r1", 
          "bihybrid_homolog_goc_score", "bihybrid_homolog_wga_coverage", 
          "bihybrid_homolog_orthology_confidence", "pcapensis_homolog_ensembl_gene", 
          "pcapensis_homolog_associated_gene_name", "pcapensis_homolog_ensembl_peptide", 
          "pcapensis_homolog_chromosome", "pcapensis_homolog_chrom_start", 
          "pcapensis_homolog_chrom_end", "pcapensis_homolog_canonical_transcript_protein", 
          "pcapensis_homolog_subtype", "pcapensis_homolog_orthology_type", 
          "pcapensis_homolog_perc_id", "pcapensis_homolog_perc_id_r1", 
          "pcapensis_homolog_goc_score", "pcapensis_homolog_wga_coverage", 
          "pcapensis_homolog_orthology_confidence", "nnaja_homolog_ensembl_gene", 
          "nnaja_homolog_associated_gene_name", "nnaja_homolog_ensembl_peptide", 
          "nnaja_homolog_chromosome", "nnaja_homolog_chrom_start", 
          "nnaja_homolog_chrom_end", "nnaja_homolog_canonical_transcript_protein", 
          "nnaja_homolog_subtype", "nnaja_homolog_orthology_type", 
          "nnaja_homolog_perc_id", "nnaja_homolog_perc_id_r1", 
          "nnaja_homolog_goc_score", "nnaja_homolog_wga_coverage", 
          "nnaja_homolog_orthology_confidence", "omelastigma_homolog_ensembl_gene", 
          "omelastigma_homolog_associated_gene_name", "omelastigma_homolog_ensembl_peptide", 
          "omelastigma_homolog_chromosome", "omelastigma_homolog_chrom_start", 
          "omelastigma_homolog_chrom_end", "omelastigma_homolog_canonical_transcript_protein", 
          "omelastigma_homolog_subtype", "omelastigma_homolog_orthology_type", 
          "omelastigma_homolog_perc_id", "omelastigma_homolog_perc_id_r1", 
          "omelastigma_homolog_goc_score", "omelastigma_homolog_wga_coverage", 
          "omelastigma_homolog_orthology_confidence", "olatipes_homolog_ensembl_gene", 
          "olatipes_homolog_associated_gene_name", "olatipes_homolog_ensembl_peptide", 
          "olatipes_homolog_chromosome", "olatipes_homolog_chrom_start", 
          "olatipes_homolog_chrom_end", "olatipes_homolog_canonical_transcript_protein", 
          "olatipes_homolog_subtype", "olatipes_homolog_orthology_type", 
          "olatipes_homolog_perc_id", "olatipes_homolog_perc_id_r1", 
          "olatipes_homolog_goc_score", "olatipes_homolog_wga_coverage", 
          "olatipes_homolog_orthology_confidence", "cjaponica_homolog_ensembl_gene", 
          "cjaponica_homolog_associated_gene_name", "cjaponica_homolog_ensembl_peptide", 
          "cjaponica_homolog_chromosome", "cjaponica_homolog_chrom_start", 
          "cjaponica_homolog_chrom_end", "cjaponica_homolog_canonical_transcript_protein", 
          "cjaponica_homolog_subtype", "cjaponica_homolog_orthology_type", 
          "cjaponica_homolog_perc_id", "cjaponica_homolog_perc_id_r1", 
          "cjaponica_homolog_goc_score", "cjaponica_homolog_wga_coverage", 
          "cjaponica_homolog_orthology_confidence", "ojavanicus_homolog_ensembl_gene", 
          "ojavanicus_homolog_associated_gene_name", "ojavanicus_homolog_ensembl_peptide", 
          "ojavanicus_homolog_chromosome", "ojavanicus_homolog_chrom_start", 
          "ojavanicus_homolog_chrom_end", "ojavanicus_homolog_canonical_transcript_protein", 
          "ojavanicus_homolog_subtype", "ojavanicus_homolog_orthology_type", 
          "ojavanicus_homolog_perc_id", "ojavanicus_homolog_perc_id_r1", 
          "ojavanicus_homolog_goc_score", "ojavanicus_homolog_wga_coverage", 
          "ojavanicus_homolog_orthology_confidence", "shabroptila_homolog_ensembl_gene", 
          "shabroptila_homolog_associated_gene_name", "shabroptila_homolog_ensembl_peptide", 
          "shabroptila_homolog_chromosome", "shabroptila_homolog_chrom_start", 
          "shabroptila_homolog_chrom_end", "shabroptila_homolog_canonical_transcript_protein", 
          "shabroptila_homolog_subtype", "shabroptila_homolog_orthology_type", 
          "shabroptila_homolog_perc_id", "shabroptila_homolog_perc_id_r1", 
          "shabroptila_homolog_goc_score", "shabroptila_homolog_wga_coverage", 
          "shabroptila_homolog_orthology_confidence", "dordii_homolog_ensembl_gene", 
          "dordii_homolog_associated_gene_name", "dordii_homolog_ensembl_peptide", 
          "dordii_homolog_chromosome", "dordii_homolog_chrom_start", 
          "dordii_homolog_chrom_end", "dordii_homolog_canonical_transcript_protein", 
          "dordii_homolog_subtype", "dordii_homolog_orthology_type", 
          "dordii_homolog_perc_id", "dordii_homolog_perc_id_r1", 
          "dordii_homolog_goc_score", "dordii_homolog_wga_coverage", 
          "dordii_homolog_orthology_confidence", "pcinereus_homolog_ensembl_gene", 
          "pcinereus_homolog_associated_gene_name", "pcinereus_homolog_ensembl_peptide", 
          "pcinereus_homolog_chromosome", "pcinereus_homolog_chrom_start", 
          "pcinereus_homolog_chrom_end", "pcinereus_homolog_canonical_transcript_protein", 
          "pcinereus_homolog_subtype", "pcinereus_homolog_orthology_type", 
          "pcinereus_homolog_perc_id", "pcinereus_homolog_perc_id_r1", 
          "pcinereus_homolog_goc_score", "pcinereus_homolog_wga_coverage", 
          "pcinereus_homolog_orthology_confidence", "pmarinus_homolog_ensembl_gene", 
          "pmarinus_homolog_associated_gene_name", "pmarinus_homolog_ensembl_peptide", 
          "pmarinus_homolog_chromosome", "pmarinus_homolog_chrom_start", 
          "pmarinus_homolog_chrom_end", "pmarinus_homolog_canonical_transcript_protein", 
          "pmarinus_homolog_subtype", "pmarinus_homolog_orthology_type", 
          "pmarinus_homolog_perc_id", "pmarinus_homolog_perc_id_r1", 
          "pmarinus_homolog_wga_coverage", "pmarinus_homolog_orthology_confidence", 
          "lcrocea_homolog_ensembl_gene", "lcrocea_homolog_associated_gene_name", 
          "lcrocea_homolog_ensembl_peptide", "lcrocea_homolog_chromosome", 
          "lcrocea_homolog_chrom_start", "lcrocea_homolog_chrom_end", 
          "lcrocea_homolog_canonical_transcript_protein", "lcrocea_homolog_subtype", 
          "lcrocea_homolog_orthology_type", "lcrocea_homolog_perc_id", 
          "lcrocea_homolog_perc_id_r1", "lcrocea_homolog_goc_score", 
          "lcrocea_homolog_wga_coverage", "lcrocea_homolog_orthology_confidence", 
          "lleishanense_homolog_ensembl_gene", "lleishanense_homolog_associated_gene_name", 
          "lleishanense_homolog_ensembl_peptide", "lleishanense_homolog_chromosome", 
          "lleishanense_homolog_chrom_start", "lleishanense_homolog_chrom_end", 
          "lleishanense_homolog_canonical_transcript_protein", 
          "lleishanense_homolog_subtype", "lleishanense_homolog_orthology_type", 
          "lleishanense_homolog_perc_id", "lleishanense_homolog_perc_id_r1", 
          "lleishanense_homolog_goc_score", "lleishanense_homolog_wga_coverage", 
          "lleishanense_homolog_orthology_confidence", "ppardus_homolog_ensembl_gene", 
          "ppardus_homolog_associated_gene_name", "ppardus_homolog_ensembl_peptide", 
          "ppardus_homolog_chromosome", "ppardus_homolog_chrom_start", 
          "ppardus_homolog_chrom_end", "ppardus_homolog_canonical_transcript_protein", 
          "ppardus_homolog_subtype", "ppardus_homolog_orthology_type", 
          "ppardus_homolog_perc_id", "ppardus_homolog_perc_id_r1", 
          "ppardus_homolog_goc_score", "ppardus_homolog_wga_coverage", 
          "ppardus_homolog_orthology_confidence", "jjaculus_homolog_ensembl_gene", 
          "jjaculus_homolog_associated_gene_name", "jjaculus_homolog_ensembl_peptide", 
          "jjaculus_homolog_chromosome", "jjaculus_homolog_chrom_start", 
          "jjaculus_homolog_chrom_end", "jjaculus_homolog_canonical_transcript_protein", 
          "jjaculus_homolog_subtype", "jjaculus_homolog_orthology_type", 
          "jjaculus_homolog_perc_id", "jjaculus_homolog_perc_id_r1", 
          "jjaculus_homolog_goc_score", "jjaculus_homolog_wga_coverage", 
          "jjaculus_homolog_orthology_confidence", "etelfairi_homolog_ensembl_gene", 
          "etelfairi_homolog_associated_gene_name", "etelfairi_homolog_ensembl_peptide", 
          "etelfairi_homolog_chromosome", "etelfairi_homolog_chrom_start", 
          "etelfairi_homolog_chrom_end", "etelfairi_homolog_canonical_transcript_protein", 
          "etelfairi_homolog_subtype", "etelfairi_homolog_orthology_type", 
          "etelfairi_homolog_perc_id", "etelfairi_homolog_perc_id_r1", 
          "etelfairi_homolog_goc_score", "etelfairi_homolog_wga_coverage", 
          "etelfairi_homolog_orthology_confidence", "pleo_homolog_ensembl_gene", 
          "pleo_homolog_associated_gene_name", "pleo_homolog_ensembl_peptide", 
          "pleo_homolog_chromosome", "pleo_homolog_chrom_start", 
          "pleo_homolog_chrom_end", "pleo_homolog_canonical_transcript_protein", 
          "pleo_homolog_subtype", "pleo_homolog_orthology_type", 
          "pleo_homolog_perc_id", "pleo_homolog_perc_id_r1", "pleo_homolog_goc_score", 
          "pleo_homolog_wga_coverage", "pleo_homolog_orthology_confidence", 
          "clanigera_homolog_ensembl_gene", "clanigera_homolog_associated_gene_name", 
          "clanigera_homolog_ensembl_peptide", "clanigera_homolog_chromosome", 
          "clanigera_homolog_chrom_start", "clanigera_homolog_chrom_end", 
          "clanigera_homolog_canonical_transcript_protein", "clanigera_homolog_subtype", 
          "clanigera_homolog_orthology_type", "clanigera_homolog_perc_id", 
          "clanigera_homolog_perc_id_r1", "clanigera_homolog_goc_score", 
          "clanigera_homolog_wga_coverage", "clanigera_homolog_orthology_confidence", 
          "clumpus_homolog_ensembl_gene", "clumpus_homolog_associated_gene_name", 
          "clumpus_homolog_ensembl_peptide", "clumpus_homolog_chromosome", 
          "clumpus_homolog_chrom_start", "clumpus_homolog_chrom_end", 
          "clumpus_homolog_canonical_transcript_protein", "clumpus_homolog_subtype", 
          "clumpus_homolog_orthology_type", "clumpus_homolog_perc_id", 
          "clumpus_homolog_perc_id_r1", "clumpus_homolog_goc_score", 
          "clumpus_homolog_wga_coverage", "clumpus_homolog_orthology_confidence", 
          "nbrichardi_homolog_ensembl_gene", "nbrichardi_homolog_associated_gene_name", 
          "nbrichardi_homolog_ensembl_peptide", "nbrichardi_homolog_chromosome", 
          "nbrichardi_homolog_chrom_start", "nbrichardi_homolog_chrom_end", 
          "nbrichardi_homolog_canonical_transcript_protein", "nbrichardi_homolog_subtype", 
          "nbrichardi_homolog_orthology_type", "nbrichardi_homolog_perc_id", 
          "nbrichardi_homolog_perc_id_r1", "nbrichardi_homolog_goc_score", 
          "nbrichardi_homolog_wga_coverage", "nbrichardi_homolog_orthology_confidence", 
          "anancymaae_homolog_ensembl_gene", "anancymaae_homolog_associated_gene_name", 
          "anancymaae_homolog_ensembl_peptide", "anancymaae_homolog_chromosome", 
          "anancymaae_homolog_chrom_start", "anancymaae_homolog_chrom_end", 
          "anancymaae_homolog_canonical_transcript_protein", "anancymaae_homolog_subtype", 
          "anancymaae_homolog_orthology_type", "anancymaae_homolog_perc_id", 
          "anancymaae_homolog_perc_id_r1", "anancymaae_homolog_goc_score", 
          "anancymaae_homolog_wga_coverage", "anancymaae_homolog_orthology_confidence", 
          "mmulatta_homolog_ensembl_gene", "mmulatta_homolog_associated_gene_name", 
          "mmulatta_homolog_ensembl_peptide", "mmulatta_homolog_chromosome", 
          "mmulatta_homolog_chrom_start", "mmulatta_homolog_chrom_end", 
          "mmulatta_homolog_canonical_transcript_protein", "mmulatta_homolog_subtype", 
          "mmulatta_homolog_orthology_type", "mmulatta_homolog_perc_id", 
          "mmulatta_homolog_perc_id_r1", "mmulatta_homolog_goc_score", 
          "mmulatta_homolog_wga_coverage", "mmulatta_homolog_orthology_confidence", 
          "nscutatus_homolog_ensembl_gene", "nscutatus_homolog_associated_gene_name", 
          "nscutatus_homolog_ensembl_peptide", "nscutatus_homolog_chromosome", 
          "nscutatus_homolog_chrom_start", "nscutatus_homolog_chrom_end", 
          "nscutatus_homolog_canonical_transcript_protein", "nscutatus_homolog_subtype", 
          "nscutatus_homolog_orthology_type", "nscutatus_homolog_perc_id", 
          "nscutatus_homolog_perc_id_r1", "nscutatus_homolog_goc_score", 
          "nscutatus_homolog_wga_coverage", "nscutatus_homolog_orthology_confidence", 
          "pnyererei_homolog_ensembl_gene", "pnyererei_homolog_associated_gene_name", 
          "pnyererei_homolog_ensembl_peptide", "pnyererei_homolog_chromosome", 
          "pnyererei_homolog_chrom_start", "pnyererei_homolog_chrom_end", 
          "pnyererei_homolog_canonical_transcript_protein", "pnyererei_homolog_subtype", 
          "pnyererei_homolog_orthology_type", "pnyererei_homolog_perc_id", 
          "pnyererei_homolog_perc_id_r1", "pnyererei_homolog_goc_score", 
          "pnyererei_homolog_wga_coverage", "pnyererei_homolog_orthology_confidence", 
          "kmarmoratus_homolog_ensembl_gene", "kmarmoratus_homolog_associated_gene_name", 
          "kmarmoratus_homolog_ensembl_peptide", "kmarmoratus_homolog_chromosome", 
          "kmarmoratus_homolog_chrom_start", "kmarmoratus_homolog_chrom_end", 
          "kmarmoratus_homolog_canonical_transcript_protein", "kmarmoratus_homolog_subtype", 
          "kmarmoratus_homolog_orthology_type", "kmarmoratus_homolog_perc_id", 
          "kmarmoratus_homolog_perc_id_r1", "kmarmoratus_homolog_goc_score", 
          "kmarmoratus_homolog_wga_coverage", "kmarmoratus_homolog_orthology_confidence", 
          "gfortis_homolog_ensembl_gene", "gfortis_homolog_associated_gene_name", 
          "gfortis_homolog_ensembl_peptide", "gfortis_homolog_chromosome", 
          "gfortis_homolog_chrom_start", "gfortis_homolog_chrom_end", 
          "gfortis_homolog_canonical_transcript_protein", "gfortis_homolog_subtype", 
          "gfortis_homolog_orthology_type", "gfortis_homolog_perc_id", 
          "gfortis_homolog_perc_id_r1", "gfortis_homolog_goc_score", 
          "gfortis_homolog_wga_coverage", "gfortis_homolog_orthology_confidence", 
          "pvampyrus_homolog_ensembl_gene", "pvampyrus_homolog_associated_gene_name", 
          "pvampyrus_homolog_ensembl_peptide", "pvampyrus_homolog_chromosome", 
          "pvampyrus_homolog_chrom_start", "pvampyrus_homolog_chrom_end", 
          "pvampyrus_homolog_canonical_transcript_protein", "pvampyrus_homolog_subtype", 
          "pvampyrus_homolog_orthology_type", "pvampyrus_homolog_perc_id", 
          "pvampyrus_homolog_perc_id_r1", "pvampyrus_homolog_goc_score", 
          "pvampyrus_homolog_wga_coverage", "pvampyrus_homolog_orthology_confidence", 
          "amexicanus_homolog_ensembl_gene", "amexicanus_homolog_associated_gene_name", 
          "amexicanus_homolog_ensembl_peptide", "amexicanus_homolog_chromosome", 
          "amexicanus_homolog_chrom_start", "amexicanus_homolog_chrom_end", 
          "amexicanus_homolog_canonical_transcript_protein", "amexicanus_homolog_subtype", 
          "amexicanus_homolog_orthology_type", "amexicanus_homolog_perc_id", 
          "amexicanus_homolog_perc_id_r1", "amexicanus_homolog_goc_score", 
          "amexicanus_homolog_wga_coverage", "amexicanus_homolog_orthology_confidence", 
          "mlucifugus_homolog_ensembl_gene", "mlucifugus_homolog_associated_gene_name", 
          "mlucifugus_homolog_ensembl_peptide", "mlucifugus_homolog_chromosome", 
          "mlucifugus_homolog_chrom_start", "mlucifugus_homolog_chrom_end", 
          "mlucifugus_homolog_canonical_transcript_protein", "mlucifugus_homolog_subtype", 
          "mlucifugus_homolog_orthology_type", "mlucifugus_homolog_perc_id", 
          "mlucifugus_homolog_perc_id_r1", "mlucifugus_homolog_goc_score", 
          "mlucifugus_homolog_wga_coverage", "mlucifugus_homolog_orthology_confidence", 
          "acitrinellus_homolog_ensembl_gene", "acitrinellus_homolog_associated_gene_name", 
          "acitrinellus_homolog_ensembl_peptide", "acitrinellus_homolog_chromosome", 
          "acitrinellus_homolog_chrom_start", "acitrinellus_homolog_chrom_end", 
          "acitrinellus_homolog_canonical_transcript_protein", 
          "acitrinellus_homolog_subtype", "acitrinellus_homolog_orthology_type", 
          "acitrinellus_homolog_perc_id", "acitrinellus_homolog_perc_id_r1", 
          "acitrinellus_homolog_goc_score", "acitrinellus_homolog_wga_coverage", 
          "acitrinellus_homolog_orthology_confidence", "mmusculus_homolog_ensembl_gene", 
          "mmusculus_homolog_associated_gene_name", "mmusculus_homolog_ensembl_peptide", 
          "mmusculus_homolog_chromosome", "mmusculus_homolog_chrom_start", 
          "mmusculus_homolog_chrom_end", "mmusculus_homolog_canonical_transcript_protein", 
          "mmusculus_homolog_subtype", "mmusculus_homolog_orthology_type", 
          "mmusculus_homolog_perc_id", "mmusculus_homolog_perc_id_r1", 
          "mmusculus_homolog_goc_score", "mmusculus_homolog_wga_coverage", 
          "mmusculus_homolog_orthology_confidence", "mmurinus_homolog_ensembl_gene", 
          "mmurinus_homolog_associated_gene_name", "mmurinus_homolog_ensembl_peptide", 
          "mmurinus_homolog_chromosome", "mmurinus_homolog_chrom_start", 
          "mmurinus_homolog_chrom_end", "mmurinus_homolog_canonical_transcript_protein", 
          "mmurinus_homolog_subtype", "mmurinus_homolog_orthology_type", 
          "mmurinus_homolog_perc_id", "mmurinus_homolog_perc_id_r1", 
          "mmurinus_homolog_goc_score", "mmurinus_homolog_wga_coverage", 
          "mmurinus_homolog_orthology_confidence", "fheteroclitus_homolog_ensembl_gene", 
          "fheteroclitus_homolog_associated_gene_name", "fheteroclitus_homolog_ensembl_peptide", 
          "fheteroclitus_homolog_chromosome", "fheteroclitus_homolog_chrom_start", 
          "fheteroclitus_homolog_chrom_end", "fheteroclitus_homolog_canonical_transcript_protein", 
          "fheteroclitus_homolog_subtype", "fheteroclitus_homolog_orthology_type", 
          "fheteroclitus_homolog_perc_id", "fheteroclitus_homolog_perc_id_r1", 
          "fheteroclitus_homolog_goc_score", "fheteroclitus_homolog_wga_coverage", 
          "fheteroclitus_homolog_orthology_confidence", "hgfemale_homolog_ensembl_gene", 
          "hgfemale_homolog_associated_gene_name", "hgfemale_homolog_ensembl_peptide", 
          "hgfemale_homolog_chromosome", "hgfemale_homolog_chrom_start", 
          "hgfemale_homolog_chrom_end", "hgfemale_homolog_canonical_transcript_protein", 
          "hgfemale_homolog_subtype", "hgfemale_homolog_orthology_type", 
          "hgfemale_homolog_perc_id", "hgfemale_homolog_perc_id_r1", 
          "hgfemale_homolog_goc_score", "hgfemale_homolog_wga_coverage", 
          "hgfemale_homolog_orthology_confidence", "mmonoceros_homolog_ensembl_gene", 
          "mmonoceros_homolog_associated_gene_name", "mmonoceros_homolog_ensembl_peptide", 
          "mmonoceros_homolog_chromosome", "mmonoceros_homolog_chrom_start", 
          "mmonoceros_homolog_chrom_end", "mmonoceros_homolog_canonical_transcript_protein", 
          "mmonoceros_homolog_subtype", "mmonoceros_homolog_orthology_type", 
          "mmonoceros_homolog_perc_id", "mmonoceros_homolog_perc_id_r1", 
          "mmonoceros_homolog_goc_score", "mmonoceros_homolog_wga_coverage", 
          "mmonoceros_homolog_orthology_confidence", "oniloticus_homolog_ensembl_gene", 
          "oniloticus_homolog_associated_gene_name", "oniloticus_homolog_ensembl_peptide", 
          "oniloticus_homolog_chromosome", "oniloticus_homolog_chrom_start", 
          "oniloticus_homolog_chrom_end", "oniloticus_homolog_canonical_transcript_protein", 
          "oniloticus_homolog_subtype", "oniloticus_homolog_orthology_type", 
          "oniloticus_homolog_perc_id", "oniloticus_homolog_perc_id_r1", 
          "oniloticus_homolog_goc_score", "oniloticus_homolog_wga_coverage", 
          "oniloticus_homolog_orthology_confidence", "pmbairdii_homolog_ensembl_gene", 
          "pmbairdii_homolog_associated_gene_name", "pmbairdii_homolog_ensembl_peptide", 
          "pmbairdii_homolog_chromosome", "pmbairdii_homolog_chrom_start", 
          "pmbairdii_homolog_chrom_end", "pmbairdii_homolog_canonical_transcript_protein", 
          "pmbairdii_homolog_subtype", "pmbairdii_homolog_orthology_type", 
          "pmbairdii_homolog_perc_id", "pmbairdii_homolog_perc_id_r1", 
          "pmbairdii_homolog_goc_score", "pmbairdii_homolog_wga_coverage", 
          "pmbairdii_homolog_orthology_confidence", "elucius_homolog_ensembl_gene", 
          "elucius_homolog_associated_gene_name", "elucius_homolog_ensembl_peptide", 
          "elucius_homolog_chromosome", "elucius_homolog_chrom_start", 
          "elucius_homolog_chrom_end", "elucius_homolog_canonical_transcript_protein", 
          "elucius_homolog_subtype", "elucius_homolog_orthology_type", 
          "elucius_homolog_perc_id", "elucius_homolog_perc_id_r1", 
          "elucius_homolog_goc_score", "elucius_homolog_wga_coverage", 
          "elucius_homolog_orthology_confidence", "panubis_homolog_ensembl_gene", 
          "panubis_homolog_associated_gene_name", "panubis_homolog_ensembl_peptide", 
          "panubis_homolog_chromosome", "panubis_homolog_chrom_start", 
          "panubis_homolog_chrom_end", "panubis_homolog_canonical_transcript_protein", 
          "panubis_homolog_subtype", "panubis_homolog_orthology_type", 
          "panubis_homolog_perc_id", "panubis_homolog_perc_id_r1", 
          "panubis_homolog_goc_score", "panubis_homolog_wga_coverage", 
          "panubis_homolog_orthology_confidence", "mdomestica_homolog_ensembl_gene", 
          "mdomestica_homolog_associated_gene_name", "mdomestica_homolog_ensembl_peptide", 
          "mdomestica_homolog_chromosome", "mdomestica_homolog_chrom_start", 
          "mdomestica_homolog_chrom_end", "mdomestica_homolog_canonical_transcript_protein", 
          "mdomestica_homolog_subtype", "mdomestica_homolog_orthology_type", 
          "mdomestica_homolog_perc_id", "mdomestica_homolog_perc_id_r1", 
          "mdomestica_homolog_goc_score", "mdomestica_homolog_wga_coverage", 
          "mdomestica_homolog_orthology_confidence", "apercula_homolog_ensembl_gene", 
          "apercula_homolog_associated_gene_name", "apercula_homolog_ensembl_peptide", 
          "apercula_homolog_chromosome", "apercula_homolog_chrom_start", 
          "apercula_homolog_chrom_end", "apercula_homolog_canonical_transcript_protein", 
          "apercula_homolog_subtype", "apercula_homolog_orthology_type", 
          "apercula_homolog_perc_id", "apercula_homolog_perc_id_r1", 
          "apercula_homolog_goc_score", "apercula_homolog_wga_coverage", 
          "apercula_homolog_orthology_confidence", "cpbellii_homolog_ensembl_gene", 
          "cpbellii_homolog_associated_gene_name", "cpbellii_homolog_ensembl_peptide", 
          "cpbellii_homolog_chromosome", "cpbellii_homolog_chrom_start", 
          "cpbellii_homolog_chrom_end", "cpbellii_homolog_canonical_transcript_protein", 
          "cpbellii_homolog_subtype", "cpbellii_homolog_orthology_type", 
          "cpbellii_homolog_perc_id", "cpbellii_homolog_perc_id_r1", 
          "cpbellii_homolog_goc_score", "cpbellii_homolog_wga_coverage", 
          "cpbellii_homolog_orthology_confidence", "pkingsleyae_homolog_ensembl_gene", 
          "pkingsleyae_homolog_associated_gene_name", "pkingsleyae_homolog_ensembl_peptide", 
          "pkingsleyae_homolog_chromosome", "pkingsleyae_homolog_chrom_start", 
          "pkingsleyae_homolog_chrom_end", "pkingsleyae_homolog_canonical_transcript_protein", 
          "pkingsleyae_homolog_subtype", "pkingsleyae_homolog_orthology_type", 
          "pkingsleyae_homolog_perc_id", "pkingsleyae_homolog_perc_id_r1", 
          "pkingsleyae_homolog_goc_score", "pkingsleyae_homolog_wga_coverage", 
          "pkingsleyae_homolog_orthology_confidence", "sscrofa_homolog_ensembl_gene", 
          "sscrofa_homolog_associated_gene_name", "sscrofa_homolog_ensembl_peptide", 
          "sscrofa_homolog_chromosome", "sscrofa_homolog_chrom_start", 
          "sscrofa_homolog_chrom_end", "sscrofa_homolog_canonical_transcript_protein", 
          "sscrofa_homolog_subtype", "sscrofa_homolog_orthology_type", 
          "sscrofa_homolog_perc_id", "sscrofa_homolog_perc_id_r1", 
          "sscrofa_homolog_goc_score", "sscrofa_homolog_wga_coverage", 
          "sscrofa_homolog_orthology_confidence", "mnemestrina_homolog_ensembl_gene", 
          "mnemestrina_homolog_associated_gene_name", "mnemestrina_homolog_ensembl_peptide", 
          "mnemestrina_homolog_chromosome", "mnemestrina_homolog_chrom_start", 
          "mnemestrina_homolog_chrom_end", "mnemestrina_homolog_canonical_transcript_protein", 
          "mnemestrina_homolog_subtype", "mnemestrina_homolog_orthology_type", 
          "mnemestrina_homolog_perc_id", "mnemestrina_homolog_perc_id_r1", 
          "mnemestrina_homolog_goc_score", "mnemestrina_homolog_wga_coverage", 
          "mnemestrina_homolog_orthology_confidence", "oprinceps_homolog_ensembl_gene", 
          "oprinceps_homolog_associated_gene_name", "oprinceps_homolog_ensembl_peptide", 
          "oprinceps_homolog_chromosome", "oprinceps_homolog_chrom_start", 
          "oprinceps_homolog_chrom_end", "oprinceps_homolog_canonical_transcript_protein", 
          "oprinceps_homolog_subtype", "oprinceps_homolog_orthology_type", 
          "oprinceps_homolog_perc_id", "oprinceps_homolog_perc_id_r1", 
          "oprinceps_homolog_goc_score", "oprinceps_homolog_wga_coverage", 
          "oprinceps_homolog_orthology_confidence", "slucioperca_homolog_ensembl_gene", 
          "slucioperca_homolog_associated_gene_name", "slucioperca_homolog_ensembl_peptide", 
          "slucioperca_homolog_chromosome", "slucioperca_homolog_chrom_start", 
          "slucioperca_homolog_chrom_end", "slucioperca_homolog_canonical_transcript_protein", 
          "slucioperca_homolog_subtype", "slucioperca_homolog_orthology_type", 
          "slucioperca_homolog_perc_id", "slucioperca_homolog_perc_id_r1", 
          "slucioperca_homolog_goc_score", "slucioperca_homolog_wga_coverage", 
          "slucioperca_homolog_orthology_confidence", "mmurdjan_homolog_ensembl_gene", 
          "mmurdjan_homolog_associated_gene_name", "mmurdjan_homolog_ensembl_peptide", 
          "mmurdjan_homolog_chromosome", "mmurdjan_homolog_chrom_start", 
          "mmurdjan_homolog_chrom_end", "mmurdjan_homolog_canonical_transcript_protein", 
          "mmurdjan_homolog_subtype", "mmurdjan_homolog_orthology_type", 
          "mmurdjan_homolog_perc_id", "mmurdjan_homolog_perc_id_r1", 
          "mmurdjan_homolog_goc_score", "mmurdjan_homolog_wga_coverage", 
          "mmurdjan_homolog_orthology_confidence", "abrachyrhynchus_homolog_ensembl_gene", 
          "abrachyrhynchus_homolog_associated_gene_name", "abrachyrhynchus_homolog_ensembl_peptide", 
          "abrachyrhynchus_homolog_chromosome", "abrachyrhynchus_homolog_chrom_start", 
          "abrachyrhynchus_homolog_chrom_end", "abrachyrhynchus_homolog_canonical_transcript_protein", 
          "abrachyrhynchus_homolog_subtype", "abrachyrhynchus_homolog_orthology_type", 
          "abrachyrhynchus_homolog_perc_id", "abrachyrhynchus_homolog_perc_id_r1", 
          "abrachyrhynchus_homolog_goc_score", "abrachyrhynchus_homolog_wga_coverage", 
          "abrachyrhynchus_homolog_orthology_confidence", "xmaculatus_homolog_ensembl_gene", 
          "xmaculatus_homolog_associated_gene_name", "xmaculatus_homolog_ensembl_peptide", 
          "xmaculatus_homolog_chromosome", "xmaculatus_homolog_chrom_start", 
          "xmaculatus_homolog_chrom_end", "xmaculatus_homolog_canonical_transcript_protein", 
          "xmaculatus_homolog_subtype", "xmaculatus_homolog_orthology_type", 
          "xmaculatus_homolog_perc_id", "xmaculatus_homolog_perc_id_r1", 
          "xmaculatus_homolog_goc_score", "xmaculatus_homolog_wga_coverage", 
          "xmaculatus_homolog_orthology_confidence", "oanatinus_homolog_ensembl_gene", 
          "oanatinus_homolog_associated_gene_name", "oanatinus_homolog_ensembl_peptide", 
          "oanatinus_homolog_chromosome", "oanatinus_homolog_chrom_start", 
          "oanatinus_homolog_chrom_end", "oanatinus_homolog_canonical_transcript_protein", 
          "oanatinus_homolog_subtype", "oanatinus_homolog_orthology_type", 
          "oanatinus_homolog_perc_id", "oanatinus_homolog_perc_id_r1", 
          "oanatinus_homolog_goc_score", "oanatinus_homolog_wga_coverage", 
          "oanatinus_homolog_orthology_confidence", "umaritimus_homolog_ensembl_gene", 
          "umaritimus_homolog_associated_gene_name", "umaritimus_homolog_ensembl_peptide", 
          "umaritimus_homolog_chromosome", "umaritimus_homolog_chrom_start", 
          "umaritimus_homolog_chrom_end", "umaritimus_homolog_canonical_transcript_protein", 
          "umaritimus_homolog_subtype", "umaritimus_homolog_orthology_type", 
          "umaritimus_homolog_perc_id", "umaritimus_homolog_perc_id_r1", 
          "umaritimus_homolog_goc_score", "umaritimus_homolog_wga_coverage", 
          "umaritimus_homolog_orthology_confidence", "mochrogaster_homolog_ensembl_gene", 
          "mochrogaster_homolog_associated_gene_name", "mochrogaster_homolog_ensembl_peptide", 
          "mochrogaster_homolog_chromosome", "mochrogaster_homolog_chrom_start", 
          "mochrogaster_homolog_chrom_end", "mochrogaster_homolog_canonical_transcript_protein", 
          "mochrogaster_homolog_subtype", "mochrogaster_homolog_orthology_type", 
          "mochrogaster_homolog_perc_id", "mochrogaster_homolog_perc_id_r1", 
          "mochrogaster_homolog_goc_score", "mochrogaster_homolog_wga_coverage", 
          "mochrogaster_homolog_orthology_confidence", "ocuniculus_homolog_ensembl_gene", 
          "ocuniculus_homolog_associated_gene_name", "ocuniculus_homolog_ensembl_peptide", 
          "ocuniculus_homolog_chromosome", "ocuniculus_homolog_chrom_start", 
          "ocuniculus_homolog_chrom_end", "ocuniculus_homolog_canonical_transcript_protein", 
          "ocuniculus_homolog_subtype", "ocuniculus_homolog_orthology_type", 
          "ocuniculus_homolog_perc_id", "ocuniculus_homolog_perc_id_r1", 
          "ocuniculus_homolog_goc_score", "ocuniculus_homolog_wga_coverage", 
          "ocuniculus_homolog_orthology_confidence", "omykiss_homolog_ensembl_gene", 
          "omykiss_homolog_associated_gene_name", "omykiss_homolog_ensembl_peptide", 
          "omykiss_homolog_chromosome", "omykiss_homolog_chrom_start", 
          "omykiss_homolog_chrom_end", "omykiss_homolog_canonical_transcript_protein", 
          "omykiss_homolog_subtype", "omykiss_homolog_orthology_type", 
          "omykiss_homolog_perc_id", "omykiss_homolog_perc_id_r1", 
          "omykiss_homolog_goc_score", "omykiss_homolog_wga_coverage", 
          "omykiss_homolog_orthology_confidence", "rnorvegicus_homolog_ensembl_gene", 
          "rnorvegicus_homolog_associated_gene_name", "rnorvegicus_homolog_ensembl_peptide", 
          "rnorvegicus_homolog_chromosome", "rnorvegicus_homolog_chrom_start", 
          "rnorvegicus_homolog_chrom_end", "rnorvegicus_homolog_canonical_transcript_protein", 
          "rnorvegicus_homolog_subtype", "rnorvegicus_homolog_orthology_type", 
          "rnorvegicus_homolog_perc_id", "rnorvegicus_homolog_perc_id_r1", 
          "rnorvegicus_homolog_goc_score", "rnorvegicus_homolog_wga_coverage", 
          "rnorvegicus_homolog_orthology_confidence", "vvulpes_homolog_ensembl_gene", 
          "vvulpes_homolog_associated_gene_name", "vvulpes_homolog_ensembl_peptide", 
          "vvulpes_homolog_chromosome", "vvulpes_homolog_chrom_start", 
          "vvulpes_homolog_chrom_end", "vvulpes_homolog_canonical_transcript_protein", 
          "vvulpes_homolog_subtype", "vvulpes_homolog_orthology_type", 
          "vvulpes_homolog_perc_id", "vvulpes_homolog_perc_id_r1", 
          "vvulpes_homolog_goc_score", "vvulpes_homolog_wga_coverage", 
          "vvulpes_homolog_orthology_confidence", "pnattereri_homolog_ensembl_gene", 
          "pnattereri_homolog_associated_gene_name", "pnattereri_homolog_ensembl_peptide", 
          "pnattereri_homolog_chromosome", "pnattereri_homolog_chrom_start", 
          "pnattereri_homolog_chrom_end", "pnattereri_homolog_canonical_transcript_protein", 
          "pnattereri_homolog_subtype", "pnattereri_homolog_orthology_type", 
          "pnattereri_homolog_perc_id", "pnattereri_homolog_perc_id_r1", 
          "pnattereri_homolog_goc_score", "pnattereri_homolog_wga_coverage", 
          "pnattereri_homolog_orthology_confidence", "ecalabaricus_homolog_ensembl_gene", 
          "ecalabaricus_homolog_associated_gene_name", "ecalabaricus_homolog_ensembl_peptide", 
          "ecalabaricus_homolog_chromosome", "ecalabaricus_homolog_chrom_start", 
          "ecalabaricus_homolog_chrom_end", "ecalabaricus_homolog_canonical_transcript_protein", 
          "ecalabaricus_homolog_subtype", "ecalabaricus_homolog_orthology_type", 
          "ecalabaricus_homolog_perc_id", "ecalabaricus_homolog_perc_id_r1", 
          "ecalabaricus_homolog_goc_score", "ecalabaricus_homolog_wga_coverage", 
          "ecalabaricus_homolog_orthology_confidence", "mcaroli_homolog_ensembl_gene", 
          "mcaroli_homolog_associated_gene_name", "mcaroli_homolog_ensembl_peptide", 
          "mcaroli_homolog_chromosome", "mcaroli_homolog_chrom_start", 
          "mcaroli_homolog_chrom_end", "mcaroli_homolog_canonical_transcript_protein", 
          "mcaroli_homolog_subtype", "mcaroli_homolog_orthology_type", 
          "mcaroli_homolog_perc_id", "mcaroli_homolog_perc_id_r1", 
          "mcaroli_homolog_goc_score", "mcaroli_homolog_wga_coverage", 
          "mcaroli_homolog_orthology_confidence", "scerevisiae_homolog_ensembl_gene", 
          "scerevisiae_homolog_associated_gene_name", "scerevisiae_homolog_ensembl_peptide", 
          "scerevisiae_homolog_chromosome", "scerevisiae_homolog_chrom_start", 
          "scerevisiae_homolog_chrom_end", "scerevisiae_homolog_canonical_transcript_protein", 
          "scerevisiae_homolog_subtype", "scerevisiae_homolog_orthology_type", 
          "scerevisiae_homolog_perc_id", "scerevisiae_homolog_perc_id_r1", 
          "scerevisiae_homolog_orthology_confidence", "platipinna_homolog_ensembl_gene", 
          "platipinna_homolog_associated_gene_name", "platipinna_homolog_ensembl_peptide", 
          "platipinna_homolog_chromosome", "platipinna_homolog_chrom_start", 
          "platipinna_homolog_chrom_end", "platipinna_homolog_canonical_transcript_protein", 
          "platipinna_homolog_subtype", "platipinna_homolog_orthology_type", 
          "platipinna_homolog_perc_id", "platipinna_homolog_perc_id_r1", 
          "platipinna_homolog_goc_score", "platipinna_homolog_wga_coverage", 
          "platipinna_homolog_orthology_confidence", "oarambouillet_homolog_ensembl_gene", 
          "oarambouillet_homolog_associated_gene_name", "oarambouillet_homolog_ensembl_peptide", 
          "oarambouillet_homolog_chromosome", "oarambouillet_homolog_chrom_start", 
          "oarambouillet_homolog_chrom_end", "oarambouillet_homolog_canonical_transcript_protein", 
          "oarambouillet_homolog_subtype", "oarambouillet_homolog_orthology_type", 
          "oarambouillet_homolog_perc_id", "oarambouillet_homolog_perc_id_r1", 
          "oarambouillet_homolog_goc_score", "oarambouillet_homolog_wga_coverage", 
          "oarambouillet_homolog_orthology_confidence", "cvariegatus_homolog_ensembl_gene", 
          "cvariegatus_homolog_associated_gene_name", "cvariegatus_homolog_ensembl_peptide", 
          "cvariegatus_homolog_chromosome", "cvariegatus_homolog_chrom_start", 
          "cvariegatus_homolog_chrom_end", "cvariegatus_homolog_canonical_transcript_protein", 
          "cvariegatus_homolog_subtype", "cvariegatus_homolog_orthology_type", 
          "cvariegatus_homolog_perc_id", "cvariegatus_homolog_perc_id_r1", 
          "cvariegatus_homolog_goc_score", "cvariegatus_homolog_wga_coverage", 
          "cvariegatus_homolog_orthology_confidence", "saraneus_homolog_ensembl_gene", 
          "saraneus_homolog_associated_gene_name", "saraneus_homolog_ensembl_peptide", 
          "saraneus_homolog_chromosome", "saraneus_homolog_chrom_start", 
          "saraneus_homolog_chrom_end", "saraneus_homolog_canonical_transcript_protein", 
          "saraneus_homolog_subtype", "saraneus_homolog_orthology_type", 
          "saraneus_homolog_perc_id", "saraneus_homolog_perc_id_r1", 
          "saraneus_homolog_goc_score", "saraneus_homolog_wga_coverage", 
          "saraneus_homolog_orthology_confidence", "mpahari_homolog_ensembl_gene", 
          "mpahari_homolog_associated_gene_name", "mpahari_homolog_ensembl_peptide", 
          "mpahari_homolog_chromosome", "mpahari_homolog_chrom_start", 
          "mpahari_homolog_chrom_end", "mpahari_homolog_canonical_transcript_protein", 
          "mpahari_homolog_subtype", "mpahari_homolog_orthology_type", 
          "mpahari_homolog_perc_id", "mpahari_homolog_perc_id_r1", 
          "mpahari_homolog_goc_score", "mpahari_homolog_wga_coverage", 
          "mpahari_homolog_orthology_confidence", "bsplendens_homolog_ensembl_gene", 
          "bsplendens_homolog_associated_gene_name", "bsplendens_homolog_ensembl_peptide", 
          "bsplendens_homolog_chromosome", "bsplendens_homolog_chrom_start", 
          "bsplendens_homolog_chrom_end", "bsplendens_homolog_canonical_transcript_protein", 
          "bsplendens_homolog_subtype", "bsplendens_homolog_orthology_type", 
          "bsplendens_homolog_perc_id", "bsplendens_homolog_perc_id_r1", 
          "bsplendens_homolog_goc_score", "bsplendens_homolog_wga_coverage", 
          "bsplendens_homolog_orthology_confidence", "mmoschiferus_homolog_ensembl_gene", 
          "mmoschiferus_homolog_associated_gene_name", "mmoschiferus_homolog_ensembl_peptide", 
          "mmoschiferus_homolog_chromosome", "mmoschiferus_homolog_chrom_start", 
          "mmoschiferus_homolog_chrom_end", "mmoschiferus_homolog_canonical_transcript_protein", 
          "mmoschiferus_homolog_subtype", "mmoschiferus_homolog_orthology_type", 
          "mmoschiferus_homolog_perc_id", "mmoschiferus_homolog_perc_id_r1", 
          "mmoschiferus_homolog_goc_score", "mmoschiferus_homolog_wga_coverage", 
          "mmoschiferus_homolog_orthology_confidence", "choffmanni_homolog_ensembl_gene", 
          "choffmanni_homolog_associated_gene_name", "choffmanni_homolog_ensembl_peptide", 
          "choffmanni_homolog_chromosome", "choffmanni_homolog_chrom_start", 
          "choffmanni_homolog_chrom_end", "choffmanni_homolog_canonical_transcript_protein", 
          "choffmanni_homolog_subtype", "choffmanni_homolog_orthology_type", 
          "choffmanni_homolog_perc_id", "choffmanni_homolog_perc_id_r1", 
          "choffmanni_homolog_goc_score", "choffmanni_homolog_wga_coverage", 
          "choffmanni_homolog_orthology_confidence", "catys_homolog_ensembl_gene", 
          "catys_homolog_associated_gene_name", "catys_homolog_ensembl_peptide", 
          "catys_homolog_chromosome", "catys_homolog_chrom_start", 
          "catys_homolog_chrom_end", "catys_homolog_canonical_transcript_protein", 
          "catys_homolog_subtype", "catys_homolog_orthology_type", 
          "catys_homolog_perc_id", "catys_homolog_perc_id_r1", 
          "catys_homolog_goc_score", "catys_homolog_wga_coverage", 
          "catys_homolog_orthology_confidence", "pcatodon_homolog_ensembl_gene", 
          "pcatodon_homolog_associated_gene_name", "pcatodon_homolog_ensembl_peptide", 
          "pcatodon_homolog_chromosome", "pcatodon_homolog_chrom_start", 
          "pcatodon_homolog_chrom_end", "pcatodon_homolog_canonical_transcript_protein", 
          "pcatodon_homolog_subtype", "pcatodon_homolog_orthology_type", 
          "pcatodon_homolog_perc_id", "pcatodon_homolog_perc_id_r1", 
          "pcatodon_homolog_goc_score", "pcatodon_homolog_wga_coverage", 
          "pcatodon_homolog_orthology_confidence", "apolyacanthus_homolog_ensembl_gene", 
          "apolyacanthus_homolog_associated_gene_name", "apolyacanthus_homolog_ensembl_peptide", 
          "apolyacanthus_homolog_chromosome", "apolyacanthus_homolog_chrom_start", 
          "apolyacanthus_homolog_chrom_end", "apolyacanthus_homolog_canonical_transcript_protein", 
          "apolyacanthus_homolog_subtype", "apolyacanthus_homolog_orthology_type", 
          "apolyacanthus_homolog_perc_id", "apolyacanthus_homolog_perc_id_r1", 
          "apolyacanthus_homolog_goc_score", "apolyacanthus_homolog_wga_coverage", 
          "apolyacanthus_homolog_orthology_confidence", "loculatus_homolog_ensembl_gene", 
          "loculatus_homolog_associated_gene_name", "loculatus_homolog_ensembl_peptide", 
          "loculatus_homolog_chromosome", "loculatus_homolog_chrom_start", 
          "loculatus_homolog_chrom_end", "loculatus_homolog_canonical_transcript_protein", 
          "loculatus_homolog_subtype", "loculatus_homolog_orthology_type", 
          "loculatus_homolog_perc_id", "loculatus_homolog_perc_id_r1", 
          "loculatus_homolog_goc_score", "loculatus_homolog_wga_coverage", 
          "loculatus_homolog_orthology_confidence", "itridecemlineatus_homolog_ensembl_gene", 
          "itridecemlineatus_homolog_associated_gene_name", "itridecemlineatus_homolog_ensembl_peptide", 
          "itridecemlineatus_homolog_chromosome", "itridecemlineatus_homolog_chrom_start", 
          "itridecemlineatus_homolog_chrom_end", "itridecemlineatus_homolog_canonical_transcript_protein", 
          "itridecemlineatus_homolog_subtype", "itridecemlineatus_homolog_orthology_type", 
          "itridecemlineatus_homolog_perc_id", "itridecemlineatus_homolog_perc_id_r1", 
          "itridecemlineatus_homolog_goc_score", "itridecemlineatus_homolog_wga_coverage", 
          "itridecemlineatus_homolog_orthology_confidence", "mspicilegus_homolog_ensembl_gene", 
          "mspicilegus_homolog_associated_gene_name", "mspicilegus_homolog_ensembl_peptide", 
          "mspicilegus_homolog_chromosome", "mspicilegus_homolog_chrom_start", 
          "mspicilegus_homolog_chrom_end", "mspicilegus_homolog_canonical_transcript_protein", 
          "mspicilegus_homolog_subtype", "mspicilegus_homolog_orthology_type", 
          "mspicilegus_homolog_perc_id", "mspicilegus_homolog_perc_id_r1", 
          "mspicilegus_homolog_goc_score", "mspicilegus_homolog_wga_coverage", 
          "mspicilegus_homolog_orthology_confidence", "gaculeatus_homolog_ensembl_gene", 
          "gaculeatus_homolog_associated_gene_name", "gaculeatus_homolog_ensembl_peptide", 
          "gaculeatus_homolog_chromosome", "gaculeatus_homolog_chrom_start", 
          "gaculeatus_homolog_chrom_end", "gaculeatus_homolog_canonical_transcript_protein", 
          "gaculeatus_homolog_subtype", "gaculeatus_homolog_orthology_type", 
          "gaculeatus_homolog_perc_id", "gaculeatus_homolog_perc_id_r1", 
          "gaculeatus_homolog_goc_score", "gaculeatus_homolog_wga_coverage", 
          "gaculeatus_homolog_orthology_confidence", "pabelii_homolog_ensembl_gene", 
          "pabelii_homolog_associated_gene_name", "pabelii_homolog_ensembl_peptide", 
          "pabelii_homolog_chromosome", "pabelii_homolog_chrom_start", 
          "pabelii_homolog_chrom_end", "pabelii_homolog_canonical_transcript_protein", 
          "pabelii_homolog_subtype", "pabelii_homolog_orthology_type", 
          "pabelii_homolog_perc_id", "pabelii_homolog_perc_id_r1", 
          "pabelii_homolog_goc_score", "pabelii_homolog_wga_coverage", 
          "pabelii_homolog_orthology_confidence", "csyrichta_homolog_ensembl_gene", 
          "csyrichta_homolog_associated_gene_name", "csyrichta_homolog_ensembl_peptide", 
          "csyrichta_homolog_chromosome", "csyrichta_homolog_chrom_start", 
          "csyrichta_homolog_chrom_end", "csyrichta_homolog_canonical_transcript_protein", 
          "csyrichta_homolog_subtype", "csyrichta_homolog_orthology_type", 
          "csyrichta_homolog_perc_id", "csyrichta_homolog_perc_id_r1", 
          "csyrichta_homolog_goc_score", "csyrichta_homolog_wga_coverage", 
          "csyrichta_homolog_orthology_confidence", "sharrisii_homolog_ensembl_gene", 
          "sharrisii_homolog_associated_gene_name", "sharrisii_homolog_ensembl_peptide", 
          "sharrisii_homolog_chromosome", "sharrisii_homolog_chrom_start", 
          "sharrisii_homolog_chrom_end", "sharrisii_homolog_canonical_transcript_protein", 
          "sharrisii_homolog_subtype", "sharrisii_homolog_orthology_type", 
          "sharrisii_homolog_perc_id", "sharrisii_homolog_perc_id_r1", 
          "sharrisii_homolog_goc_score", "sharrisii_homolog_orthology_confidence", 
          "tnigroviridis_homolog_ensembl_gene", "tnigroviridis_homolog_associated_gene_name", 
          "tnigroviridis_homolog_ensembl_peptide", "tnigroviridis_homolog_chromosome", 
          "tnigroviridis_homolog_chrom_start", "tnigroviridis_homolog_chrom_end", 
          "tnigroviridis_homolog_canonical_transcript_protein", 
          "tnigroviridis_homolog_subtype", "tnigroviridis_homolog_orthology_type", 
          "tnigroviridis_homolog_perc_id", "tnigroviridis_homolog_perc_id_r1", 
          "tnigroviridis_homolog_goc_score", "tnigroviridis_homolog_wga_coverage", 
          "tnigroviridis_homolog_orthology_confidence", "tctriunguis_homolog_ensembl_gene", 
          "tctriunguis_homolog_associated_gene_name", "tctriunguis_homolog_ensembl_peptide", 
          "tctriunguis_homolog_chromosome", "tctriunguis_homolog_chrom_start", 
          "tctriunguis_homolog_chrom_end", "tctriunguis_homolog_canonical_transcript_protein", 
          "tctriunguis_homolog_subtype", "tctriunguis_homolog_orthology_type", 
          "tctriunguis_homolog_perc_id", "tctriunguis_homolog_perc_id_r1", 
          "tctriunguis_homolog_goc_score", "tctriunguis_homolog_wga_coverage", 
          "tctriunguis_homolog_orthology_confidence", "ptaltaica_homolog_ensembl_gene", 
          "ptaltaica_homolog_associated_gene_name", "ptaltaica_homolog_ensembl_peptide", 
          "ptaltaica_homolog_chromosome", "ptaltaica_homolog_chrom_start", 
          "ptaltaica_homolog_chrom_end", "ptaltaica_homolog_canonical_transcript_protein", 
          "ptaltaica_homolog_subtype", "ptaltaica_homolog_orthology_type", 
          "ptaltaica_homolog_perc_id", "ptaltaica_homolog_perc_id_r1", 
          "ptaltaica_homolog_goc_score", "ptaltaica_homolog_wga_coverage", 
          "ptaltaica_homolog_orthology_confidence", "hcomes_homolog_ensembl_gene", 
          "hcomes_homolog_associated_gene_name", "hcomes_homolog_ensembl_peptide", 
          "hcomes_homolog_chromosome", "hcomes_homolog_chrom_start", 
          "hcomes_homolog_chrom_end", "hcomes_homolog_canonical_transcript_protein", 
          "hcomes_homolog_subtype", "hcomes_homolog_orthology_type", 
          "hcomes_homolog_perc_id", "hcomes_homolog_perc_id_r1", 
          "hcomes_homolog_goc_score", "hcomes_homolog_wga_coverage", 
          "hcomes_homolog_orthology_confidence", "csemilaevis_homolog_ensembl_gene", 
          "csemilaevis_homolog_associated_gene_name", "csemilaevis_homolog_ensembl_peptide", 
          "csemilaevis_homolog_chromosome", "csemilaevis_homolog_chrom_start", 
          "csemilaevis_homolog_chrom_end", "csemilaevis_homolog_canonical_transcript_protein", 
          "csemilaevis_homolog_subtype", "csemilaevis_homolog_orthology_type", 
          "csemilaevis_homolog_perc_id", "csemilaevis_homolog_perc_id_r1", 
          "csemilaevis_homolog_goc_score", "csemilaevis_homolog_wga_coverage", 
          "csemilaevis_homolog_orthology_confidence", "tbelangeri_homolog_ensembl_gene", 
          "tbelangeri_homolog_associated_gene_name", "tbelangeri_homolog_ensembl_peptide", 
          "tbelangeri_homolog_chromosome", "tbelangeri_homolog_chrom_start", 
          "tbelangeri_homolog_chrom_end", "tbelangeri_homolog_canonical_transcript_protein", 
          "tbelangeri_homolog_subtype", "tbelangeri_homolog_orthology_type", 
          "tbelangeri_homolog_perc_id", "tbelangeri_homolog_perc_id_r1", 
          "tbelangeri_homolog_goc_score", "tbelangeri_homolog_wga_coverage", 
          "tbelangeri_homolog_orthology_confidence", "xtropicalis_homolog_ensembl_gene", 
          "xtropicalis_homolog_associated_gene_name", "xtropicalis_homolog_ensembl_peptide", 
          "xtropicalis_homolog_chromosome", "xtropicalis_homolog_chrom_start", 
          "xtropicalis_homolog_chrom_end", "xtropicalis_homolog_canonical_transcript_protein", 
          "xtropicalis_homolog_subtype", "xtropicalis_homolog_orthology_type", 
          "xtropicalis_homolog_perc_id", "xtropicalis_homolog_perc_id_r1", 
          "xtropicalis_homolog_goc_score", "xtropicalis_homolog_wga_coverage", 
          "xtropicalis_homolog_orthology_confidence", "spunctatus_homolog_ensembl_gene", 
          "spunctatus_homolog_associated_gene_name", "spunctatus_homolog_ensembl_peptide", 
          "spunctatus_homolog_chromosome", "spunctatus_homolog_chrom_start", 
          "spunctatus_homolog_chrom_end", "spunctatus_homolog_canonical_transcript_protein", 
          "spunctatus_homolog_subtype", "spunctatus_homolog_orthology_type", 
          "spunctatus_homolog_perc_id", "spunctatus_homolog_perc_id_r1", 
          "spunctatus_homolog_goc_score", "spunctatus_homolog_wga_coverage", 
          "spunctatus_homolog_orthology_confidence", "smaximus_homolog_ensembl_gene", 
          "smaximus_homolog_associated_gene_name", "smaximus_homolog_ensembl_peptide", 
          "smaximus_homolog_chromosome", "smaximus_homolog_chrom_start", 
          "smaximus_homolog_chrom_end", "smaximus_homolog_canonical_transcript_protein", 
          "smaximus_homolog_subtype", "smaximus_homolog_orthology_type", 
          "smaximus_homolog_perc_id", "smaximus_homolog_perc_id_r1", 
          "smaximus_homolog_goc_score", "smaximus_homolog_orthology_confidence", 
          "mgallopavo_homolog_ensembl_gene", "mgallopavo_homolog_associated_gene_name", 
          "mgallopavo_homolog_ensembl_peptide", "mgallopavo_homolog_chromosome", 
          "mgallopavo_homolog_chrom_start", "mgallopavo_homolog_chrom_end", 
          "mgallopavo_homolog_canonical_transcript_protein", "mgallopavo_homolog_subtype", 
          "mgallopavo_homolog_orthology_type", "mgallopavo_homolog_perc_id", 
          "mgallopavo_homolog_perc_id_r1", "mgallopavo_homolog_goc_score", 
          "mgallopavo_homolog_orthology_confidence", "nfurzeri_homolog_ensembl_gene", 
          "nfurzeri_homolog_associated_gene_name", "nfurzeri_homolog_ensembl_peptide", 
          "nfurzeri_homolog_chromosome", "nfurzeri_homolog_chrom_start", 
          "nfurzeri_homolog_chrom_end", "nfurzeri_homolog_canonical_transcript_protein", 
          "nfurzeri_homolog_subtype", "nfurzeri_homolog_orthology_type", 
          "nfurzeri_homolog_perc_id", "nfurzeri_homolog_perc_id_r1", 
          "nfurzeri_homolog_goc_score", "nfurzeri_homolog_wga_coverage", 
          "nfurzeri_homolog_orthology_confidence", "ngalili_homolog_ensembl_gene", 
          "ngalili_homolog_associated_gene_name", "ngalili_homolog_ensembl_peptide", 
          "ngalili_homolog_chromosome", "ngalili_homolog_chrom_start", 
          "ngalili_homolog_chrom_end", "ngalili_homolog_canonical_transcript_protein", 
          "ngalili_homolog_subtype", "ngalili_homolog_orthology_type", 
          "ngalili_homolog_perc_id", "ngalili_homolog_perc_id_r1", 
          "ngalili_homolog_goc_score", "ngalili_homolog_wga_coverage", 
          "ngalili_homolog_orthology_confidence", "psinus_homolog_ensembl_gene", 
          "psinus_homolog_associated_gene_name", "psinus_homolog_ensembl_peptide", 
          "psinus_homolog_chromosome", "psinus_homolog_chrom_start", 
          "psinus_homolog_chrom_end", "psinus_homolog_canonical_transcript_protein", 
          "psinus_homolog_subtype", "psinus_homolog_orthology_type", 
          "psinus_homolog_perc_id", "psinus_homolog_perc_id_r1", 
          "psinus_homolog_goc_score", "psinus_homolog_wga_coverage", 
          "psinus_homolog_orthology_confidence", "csabaeus_homolog_ensembl_gene", 
          "csabaeus_homolog_associated_gene_name", "csabaeus_homolog_ensembl_peptide", 
          "csabaeus_homolog_chromosome", "csabaeus_homolog_chrom_start", 
          "csabaeus_homolog_chrom_end", "csabaeus_homolog_canonical_transcript_protein", 
          "csabaeus_homolog_subtype", "csabaeus_homolog_orthology_type", 
          "csabaeus_homolog_perc_id", "csabaeus_homolog_perc_id_r1", 
          "csabaeus_homolog_goc_score", "csabaeus_homolog_wga_coverage", 
          "csabaeus_homolog_orthology_confidence", "neugenii_homolog_ensembl_gene", 
          "neugenii_homolog_associated_gene_name", "neugenii_homolog_ensembl_peptide", 
          "neugenii_homolog_chromosome", "neugenii_homolog_chrom_start", 
          "neugenii_homolog_chrom_end", "neugenii_homolog_canonical_transcript_protein", 
          "neugenii_homolog_subtype", "neugenii_homolog_orthology_type", 
          "neugenii_homolog_perc_id", "neugenii_homolog_perc_id_r1", 
          "neugenii_homolog_goc_score", "neugenii_homolog_wga_coverage", 
          "neugenii_homolog_orthology_confidence", "cjacchus_homolog_ensembl_gene", 
          "cjacchus_homolog_associated_gene_name", "cjacchus_homolog_ensembl_peptide", 
          "cjacchus_homolog_chromosome", "cjacchus_homolog_chrom_start", 
          "cjacchus_homolog_chrom_end", "cjacchus_homolog_canonical_transcript_protein", 
          "cjacchus_homolog_subtype", "cjacchus_homolog_orthology_type", 
          "cjacchus_homolog_perc_id", "cjacchus_homolog_perc_id_r1", 
          "cjacchus_homolog_goc_score", "cjacchus_homolog_wga_coverage", 
          "cjacchus_homolog_orthology_confidence", "bmutus_homolog_ensembl_gene", 
          "bmutus_homolog_associated_gene_name", "bmutus_homolog_ensembl_peptide", 
          "bmutus_homolog_chromosome", "bmutus_homolog_chrom_start", 
          "bmutus_homolog_chrom_end", "bmutus_homolog_canonical_transcript_protein", 
          "bmutus_homolog_subtype", "bmutus_homolog_orthology_type", 
          "bmutus_homolog_perc_id", "bmutus_homolog_perc_id_r1", 
          "bmutus_homolog_goc_score", "bmutus_homolog_wga_coverage", 
          "bmutus_homolog_orthology_confidence", "chyarkandensis_homolog_ensembl_gene", 
          "chyarkandensis_homolog_associated_gene_name", "chyarkandensis_homolog_ensembl_peptide", 
          "chyarkandensis_homolog_chromosome", "chyarkandensis_homolog_chrom_start", 
          "chyarkandensis_homolog_chrom_end", "chyarkandensis_homolog_canonical_transcript_protein", 
          "chyarkandensis_homolog_subtype", "chyarkandensis_homolog_orthology_type", 
          "chyarkandensis_homolog_perc_id", "chyarkandensis_homolog_perc_id_r1", 
          "chyarkandensis_homolog_goc_score", "chyarkandensis_homolog_wga_coverage", 
          "chyarkandensis_homolog_orthology_confidence", "sldorsalis_homolog_ensembl_gene", 
          "sldorsalis_homolog_associated_gene_name", "sldorsalis_homolog_ensembl_peptide", 
          "sldorsalis_homolog_chromosome", "sldorsalis_homolog_chrom_start", 
          "sldorsalis_homolog_chrom_end", "sldorsalis_homolog_canonical_transcript_protein", 
          "sldorsalis_homolog_subtype", "sldorsalis_homolog_orthology_type", 
          "sldorsalis_homolog_perc_id", "sldorsalis_homolog_perc_id_r1", 
          "sldorsalis_homolog_goc_score", "sldorsalis_homolog_wga_coverage", 
          "sldorsalis_homolog_orthology_confidence", "tguttata_homolog_ensembl_gene", 
          "tguttata_homolog_associated_gene_name", "tguttata_homolog_ensembl_peptide", 
          "tguttata_homolog_chromosome", "tguttata_homolog_chrom_start", 
          "tguttata_homolog_chrom_end", "tguttata_homolog_canonical_transcript_protein", 
          "tguttata_homolog_subtype", "tguttata_homolog_orthology_type", 
          "tguttata_homolog_perc_id", "tguttata_homolog_perc_id_r1", 
          "tguttata_homolog_goc_score", "tguttata_homolog_wga_coverage", 
          "tguttata_homolog_orthology_confidence", "mzebra_homolog_ensembl_gene", 
          "mzebra_homolog_associated_gene_name", "mzebra_homolog_ensembl_peptide", 
          "mzebra_homolog_chromosome", "mzebra_homolog_chrom_start", 
          "mzebra_homolog_chrom_end", "mzebra_homolog_canonical_transcript_protein", 
          "mzebra_homolog_subtype", "mzebra_homolog_orthology_type", 
          "mzebra_homolog_perc_id", "mzebra_homolog_perc_id_r1", 
          "mzebra_homolog_goc_score", "mzebra_homolog_wga_coverage", 
          "mzebra_homolog_orthology_confidence", "drerio_homolog_ensembl_gene", 
          "drerio_homolog_associated_gene_name", "drerio_homolog_ensembl_peptide", 
          "drerio_homolog_chromosome", "drerio_homolog_chrom_start", 
          "drerio_homolog_chrom_end", "drerio_homolog_canonical_transcript_protein", 
          "drerio_homolog_subtype", "drerio_homolog_orthology_type", 
          "drerio_homolog_perc_id", "drerio_homolog_perc_id_r1", 
          "drerio_homolog_goc_score", "drerio_homolog_wga_coverage", 
          "drerio_homolog_orthology_confidence", "marmatus_homolog_ensembl_gene", 
          "marmatus_homolog_associated_gene_name", "marmatus_homolog_ensembl_peptide", 
          "marmatus_homolog_chromosome", "marmatus_homolog_chrom_start", 
          "marmatus_homolog_chrom_end", "marmatus_homolog_canonical_transcript_protein", 
          "marmatus_homolog_subtype", "marmatus_homolog_orthology_type", 
          "marmatus_homolog_perc_id", "marmatus_homolog_perc_id_r1", 
          "marmatus_homolog_goc_score", "marmatus_homolog_orthology_confidence", 
          "hsapiens_paralog_ensembl_gene", "hsapiens_paralog_associated_gene_name", 
          "hsapiens_paralog_ensembl_peptide", "hsapiens_paralog_chromosome", 
          "hsapiens_paralog_chrom_start", "hsapiens_paralog_chrom_end", 
          "hsapiens_paralog_canonical_transcript_protein", "hsapiens_paralog_subtype", 
          "hsapiens_paralog_orthology_type", "hsapiens_paralog_perc_id", 
          "hsapiens_paralog_perc_id_r1", "ensembl_gene_id", "ensembl_gene_id_version", 
          "version", "ensembl_transcript_id", "ensembl_transcript_id_version", 
          "transcript_version", "ensembl_peptide_id", "ensembl_peptide_id_version", 
          "peptide_version", "chromosome_name", "start_position", 
          "end_position", "strand", "band", "external_gene_name", 
          "external_gene_source", "transcript_count", "percentage_gene_gc_content", 
          "description", "variation_name", "germ_line_variation_source", 
          "source_description", "allele", "validated", "mapweight", 
          "minor_allele", "minor_allele_freq", "minor_allele_count", 
          "clinical_significance", "transcript_location", "snp_chromosome_strand", 
          "peptide_location", "chromosome_start", "chromosome_end", 
          "polyphen_prediction_2076", "polyphen_score_2076", "sift_prediction_2076", 
          "sift_score_2076", "distance_to_transcript_2076", "cds_start_2076", 
          "cds_end_2076", "peptide_shift", "synonymous_status", 
          "allele_string_2076", "transcript_exon_intron", "gene_exon_intron", 
          "transcript_flank", "gene_flank", "coding_transcript_flank", 
          "coding_gene_flank", "5utr", "3utr", "gene_exon", "cdna", 
          "coding", "peptide", "upstream_flank", "downstream_flank", 
          "ensembl_gene_id", "ensembl_gene_id_version", "description", 
          "external_gene_name", "external_gene_source", "chromosome_name", 
          "start_position", "end_position", "gene_biotype", "version", 
          "uniparc", "uniprotswissprot", "uniprotsptrembl", "cdna_coding_start", 
          "cdna_coding_end", "5_utr_start", "5_utr_end", "3_utr_start", 
          "3_utr_end", "ensembl_transcript_id", "ensembl_transcript_id_version", 
          "ensembl_peptide_id", "ensembl_peptide_id_version", "transcript_biotype", 
          "transcript_version", "peptide_version", "strand", "transcript_start", 
          "transcript_end", "transcription_start_site", "transcript_length", 
          "cds_length", "cds_start", "cds_end", "ensembl_exon_id", 
          "exon_chrom_start", "exon_chrom_end", "strand", "rank", 
          "phase", "end_phase", "cdna_coding_start", "cdna_coding_end", 
          "genomic_coding_start", "genomic_coding_end", "is_constitutive"
          ), description = c("Gene stable ID", "Gene stable ID version", 
          "Transcript stable ID", "Transcript stable ID version", 
          "Protein stable ID", "Protein stable ID version", "Exon stable ID", 
          "Gene description", "Chromosome/scaffold name", "Gene start (bp)", 
          "Gene end (bp)", "Strand", "Karyotype band", "Transcript start (bp)", 
          "Transcript end (bp)", "Transcription start site (TSS)", 
          "Transcript length (including UTRs and CDS)", "Transcript support level (TSL)", 
          "GENCODE basic annotation", "APPRIS annotation", "Ensembl Canonical", 
          "RefSeq match transcript (MANE Select)", "RefSeq match transcript (MANE Plus Clinical)", 
          "Gene name", "Source of gene name", "Transcript name", 
          "Source of transcript name", "Transcript count", "Gene % GC content", 
          "Gene type", "Transcript type", "Source (gene)", "Source (transcript)", 
          "Version (gene)", "Version (transcript)", "Version (protein)", 
          "Gene Synonym", "Phenotype description", "Source name", 
          "Study external reference", "Strain name", "Strain gender", 
          "P value", "GO term accession", "GO term name", "GO term definition", 
          "GO term evidence code", "GO domain", "GOSlim GOA Accession(s)", 
          "GOSlim GOA Description", "BioGRID Interaction data, The General Repository for Interaction Datasets ID", 
          "CCDS ID", "ChEMBL ID", "DataBase of Aberrant 3' Splice Sites name", 
          "DataBase of Aberrant 3' Splice Sites ID", "DataBase of Aberrant 5' Splice Sites name", 
          "DataBase of Aberrant 5' Splice Sites ID", "Ensembl Human Transcript ID", 
          "Ensembl Human Translation ID", "EntrezGene transcript name ID", 
          "European Nucleotide Archive ID", "Expression Atlas ID", 
          "GeneDB ID", "HGNC ID", "HGNC symbol", "Human Protein Atlas accession", 
          "Human Protein Atlas ID", "INSDC protein ID", "LRG display in Ensembl gene ID", 
          "LRG display in Ensembl transcript ID", "MEROPS - the Peptidase Database ID", 
          "MIM gene description", "MIM gene accession", "MIM morbid description", 
          "MIM morbid accession", "miRBase accession", "miRBase ID", 
          "miRBase transcript name ID", "NCBI gene (formerly Entrezgene) description", 
          "NCBI gene (formerly Entrezgene) accession", "NCBI gene (formerly Entrezgene) ID", 
          "PDB ID", "Reactome ID", "Reactome gene ID", "Reactome transcript ID", 
          "RefSeq mRNA ID", "RefSeq mRNA predicted ID", "RefSeq ncRNA ID", 
          "RefSeq ncRNA predicted ID", "RefSeq peptide ID", "RefSeq peptide predicted ID", 
          "RFAM ID", "RFAM transcript name ID", "RNAcentral ID", 
          "Transcript name ID", "UCSC Stable ID", "UniParc ID", 
          "UniProtKB Gene Name symbol", "UniProtKB Gene Name ID", 
          "UniProtKB isoform ID", "UniProtKB/Swiss-Prot ID", "UniProtKB/TrEMBL ID", 
          "WikiGene description", "WikiGene name", "WikiGene ID", 
          "AFFY HC G110 probe", "AFFY HG Focus probe", "AFFY HG U133A probe", 
          "AFFY HG U133A 2 probe", "AFFY HG U133B probe", "AFFY HG U133 Plus 2 probe", 
          "AFFY HG U95A probe", "AFFY HG U95Av2 probe", "AFFY HG U95B probe", 
          "AFFY HG U95C probe", "AFFY HG U95D probe", "AFFY HG U95E probe", 
          "AFFY HTA 2 0 probe", "AFFY HuEx 1 0 st v2 probe", "AFFY HuGeneFL probe", 
          "AFFY HuGene 1 0 st v1 probe", "AFFY HuGene 2 0 st v1 probe", 
          "AFFY HuGene 2 1 st v1 probe", "AFFY PrimeView probe", 
          "AFFY U133 X3P probe", "AGILENT CGH 44b probe", "AGILENT GPL26966 probe", 
          "AGILENT GPL6848 probe", "AGILENT SurePrint G3 GE 8x60k probe", 
          "AGILENT SurePrint G3 GE 8x60k v2 probe", "AGILENT WholeGenome probe", 
          "AGILENT WholeGenome 4x44k v1 probe", "AGILENT WholeGenome 4x44k v2 probe", 
          "CODELINK CODELINK probe", "ILLUMINA HumanHT 12 V3 probe", 
          "ILLUMINA HumanHT 12 V4 probe", "ILLUMINA HumanRef 8 V3 probe", 
          "ILLUMINA HumanWG 6 V1 probe", "ILLUMINA HumanWG 6 V2 probe", 
          "ILLUMINA HumanWG 6 V3 probe", "PHALANX OneArray probe", 
          "CDD ID", "CDD start", "CDD end", "Gene3D ID", "Gene3D start", 
          "Gene3D end", "HAMAP ID", "HAMAP start", "HAMAP end", 
          "PANTHER ID", "PANTHER start", "PANTHER end", "Pfam ID", 
          "Pfam start", "Pfam end", "PIRSF ID", "PIRSF start", 
          "PIRSF end", "Prints ID", "Prints start", "Prints end", 
          "PROSITE patterns ID", "PROSITE patterns start", "PROSITE patterns end", 
          "PROSITE profiles ID", "PROSITE profiles start", "PROSITE profiles end", 
          "SFLD ID", "SFLD start", "SFLD end", "SMART ID", "SMART start", 
          "SMART end", "Superfamily ID", "Superfamily start", "Superfamily end", 
          "TIGRFAM ID", "TIGRFAM start", "TIGRFAM end", "Interpro ID", 
          "Interpro Short Description", "Interpro Description", 
          "Interpro start", "Interpro end", "MobiDB lite", "MobiDB lite start", 
          "MobiDB lite end", "Coiled-coils (Ncoils)", "Coiled-coils (Ncoils) start", 
          "Coiled-coils (Ncoils) end", "Low complexity (Seg)", 
          "Low complexity (Seg) start", "Low complexity (Seg) end", 
          "PDB-ENSP mappings", "PDB-ENSP mappings start", "PDB-ENSP mappings end", 
          "Cleavage site (Signalp)", "Cleavage site (Signalp) start", 
          "Cleavage site (Signalp) end", "Transmembrane helices", 
          "Transmembrane helices start", "Transmembrane helices end", 
          "Gene stable ID", "Gene stable ID version", "Version (gene)", 
          "Transcript stable ID", "Transcript stable ID version", 
          "Version (transcript)", "Protein stable ID", "Protein stable ID version", 
          "Version (protein)", "Chromosome/scaffold name", "Gene start (bp)", 
          "Gene end (bp)", "Transcript start (bp)", "Transcript end (bp)", 
          "Transcription start site (TSS)", "Transcript length (including UTRs and CDS)", 
          "Strand", "Gene name", "Source of gene name", "5' UTR start", 
          "5' UTR end", "3' UTR start", "3' UTR end", "CDS Length", 
          "Transcript count", "Gene description", "Gene type", 
          "Exon region start (bp)", "Exon region end (bp)", "Constitutive exon", 
          "Exon rank in transcript", "Start phase", "End phase", 
          "cDNA coding start", "cDNA coding end", "Genomic coding start", 
          "Genomic coding end", "Exon stable ID", "CDS start", 
          "CDS end", "Gene stable ID", "Gene stable ID version", 
          "Version (gene)", "Transcript stable ID", "Transcript stable ID version", 
          "Version (transcript)", "Protein stable ID", "Protein stable ID version", 
          "Version (protein)", "Chromosome/scaffold name", "Gene start (bp)", 
          "Gene end (bp)", "Strand", "Karyotype band", "Gene name", 
          "Source of gene name", "Transcript count", "Gene % GC content", 
          "Gene description", "Abingdon island giant tortoise gene stable ID", 
          "Abingdon island giant tortoise gene name", "Abingdon island giant tortoise protein or transcript stable ID", 
          "Abingdon island giant tortoise chromosome/scaffold name", 
          "Abingdon island giant tortoise chromosome/scaffold start (bp)", 
          "Abingdon island giant tortoise chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Abingdon island giant tortoise", 
          "Abingdon island giant tortoise homology type", "%id. target Abingdon island giant tortoise gene identical to query gene", 
          "%id. query gene identical to target Abingdon island giant tortoise gene", 
          "Abingdon island giant tortoise Gene-order conservation score", 
          "Abingdon island giant tortoise Whole-genome alignment coverage", 
          "Abingdon island giant tortoise orthology confidence [0 low, 1 high]", 
          "African ostrich gene stable ID", "African ostrich gene name", 
          "African ostrich protein or transcript stable ID", "African ostrich chromosome/scaffold name", 
          "African ostrich chromosome/scaffold start (bp)", "African ostrich chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with African ostrich", 
          "African ostrich homology type", "%id. target African ostrich gene identical to query gene", 
          "%id. query gene identical to target African ostrich gene", 
          "African ostrich Gene-order conservation score", "African ostrich Whole-genome alignment coverage", 
          "African ostrich orthology confidence [0 low, 1 high]", 
          "Algerian mouse gene stable ID", "Algerian mouse gene name", 
          "Algerian mouse protein or transcript stable ID", "Algerian mouse chromosome/scaffold name", 
          "Algerian mouse chromosome/scaffold start (bp)", "Algerian mouse chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Algerian mouse", 
          "Algerian mouse homology type", "%id. target Algerian mouse gene identical to query gene", 
          "%id. query gene identical to target Algerian mouse gene", 
          "Algerian mouse Gene-order conservation score", "Algerian mouse Whole-genome alignment coverage", 
          "Algerian mouse orthology confidence [0 low, 1 high]", 
          "Alpaca gene stable ID", "Alpaca gene name", "Alpaca protein or transcript stable ID", 
          "Alpaca chromosome/scaffold name", "Alpaca chromosome/scaffold start (bp)", 
          "Alpaca chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Alpaca", "Alpaca homology type", 
          "%id. target Alpaca gene identical to query gene", "%id. query gene identical to target Alpaca gene", 
          "Alpaca Gene-order conservation score", "Alpaca Whole-genome alignment coverage", 
          "Alpaca orthology confidence [0 low, 1 high]", "Alpine marmot gene stable ID", 
          "Alpine marmot gene name", "Alpine marmot protein or transcript stable ID", 
          "Alpine marmot chromosome/scaffold name", "Alpine marmot chromosome/scaffold start (bp)", 
          "Alpine marmot chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Alpine marmot", "Alpine marmot homology type", 
          "%id. target Alpine marmot gene identical to query gene", 
          "%id. query gene identical to target Alpine marmot gene", 
          "Alpine marmot Gene-order conservation score", "Alpine marmot Whole-genome alignment coverage", 
          "Alpine marmot orthology confidence [0 low, 1 high]", 
          "Amazon molly gene stable ID", "Amazon molly gene name", 
          "Amazon molly protein or transcript stable ID", "Amazon molly chromosome/scaffold name", 
          "Amazon molly chromosome/scaffold start (bp)", "Amazon molly chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Amazon molly", 
          "Amazon molly homology type", "%id. target Amazon molly gene identical to query gene", 
          "%id. query gene identical to target Amazon molly gene", 
          "Amazon molly Gene-order conservation score", "Amazon molly Whole-genome alignment coverage", 
          "Amazon molly orthology confidence [0 low, 1 high]", 
          "American bison gene stable ID", "American bison gene name", 
          "American bison protein or transcript stable ID", "American bison chromosome/scaffold name", 
          "American bison chromosome/scaffold start (bp)", "American bison chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with American bison", 
          "American bison homology type", "%id. target American bison gene identical to query gene", 
          "%id. query gene identical to target American bison gene", 
          "American bison Gene-order conservation score", "American bison Whole-genome alignment coverage", 
          "American bison orthology confidence [0 low, 1 high]", 
          "American black bear gene stable ID", "American black bear gene name", 
          "American black bear protein or transcript stable ID", 
          "American black bear chromosome/scaffold name", "American black bear chromosome/scaffold start (bp)", 
          "American black bear chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with American black bear", "American black bear homology type", 
          "%id. target American black bear gene identical to query gene", 
          "%id. query gene identical to target American black bear gene", 
          "American black bear Gene-order conservation score", 
          "American black bear Whole-genome alignment coverage", 
          "American black bear orthology confidence [0 low, 1 high]", 
          "American mink gene stable ID", "American mink gene name", 
          "American mink protein or transcript stable ID", "American mink chromosome/scaffold name", 
          "American mink chromosome/scaffold start (bp)", "American mink chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with American mink", 
          "American mink homology type", "%id. target American mink gene identical to query gene", 
          "%id. query gene identical to target American mink gene", 
          "American mink Gene-order conservation score", "American mink Whole-genome alignment coverage", 
          "American mink orthology confidence [0 low, 1 high]", 
          "Arabian camel gene stable ID", "Arabian camel gene name", 
          "Arabian camel protein or transcript stable ID", "Arabian camel chromosome/scaffold name", 
          "Arabian camel chromosome/scaffold start (bp)", "Arabian camel chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Arabian camel", 
          "Arabian camel homology type", "%id. target Arabian camel gene identical to query gene", 
          "%id. query gene identical to target Arabian camel gene", 
          "Arabian camel Gene-order conservation score", "Arabian camel Whole-genome alignment coverage", 
          "Arabian camel orthology confidence [0 low, 1 high]", 
          "Arctic ground squirrel gene stable ID", "Arctic ground squirrel gene name", 
          "Arctic ground squirrel protein or transcript stable ID", 
          "Arctic ground squirrel chromosome/scaffold name", "Arctic ground squirrel chromosome/scaffold start (bp)", 
          "Arctic ground squirrel chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Arctic ground squirrel", 
          "Arctic ground squirrel homology type", "%id. target Arctic ground squirrel gene identical to query gene", 
          "%id. query gene identical to target Arctic ground squirrel gene", 
          "Arctic ground squirrel Gene-order conservation score", 
          "Arctic ground squirrel Whole-genome alignment coverage", 
          "Arctic ground squirrel orthology confidence [0 low, 1 high]", 
          "Argentine black and white tegu gene stable ID", "Argentine black and white tegu gene name", 
          "Argentine black and white tegu protein or transcript stable ID", 
          "Argentine black and white tegu chromosome/scaffold name", 
          "Argentine black and white tegu chromosome/scaffold start (bp)", 
          "Argentine black and white tegu chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Argentine black and white tegu", 
          "Argentine black and white tegu homology type", "%id. target Argentine black and white tegu gene identical to query gene", 
          "%id. query gene identical to target Argentine black and white tegu gene", 
          "Argentine black and white tegu Gene-order conservation score", 
          "Argentine black and white tegu Whole-genome alignment coverage", 
          "Argentine black and white tegu orthology confidence [0 low, 1 high]", 
          "Armadillo gene stable ID", "Armadillo gene name", "Armadillo protein or transcript stable ID", 
          "Armadillo chromosome/scaffold name", "Armadillo chromosome/scaffold start (bp)", 
          "Armadillo chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Armadillo", "Armadillo homology type", 
          "%id. target Armadillo gene identical to query gene", 
          "%id. query gene identical to target Armadillo gene", 
          "Armadillo Gene-order conservation score", "Armadillo Whole-genome alignment coverage", 
          "Armadillo orthology confidence [0 low, 1 high]", "Asian bonytongue gene stable ID", 
          "Asian bonytongue gene name", "Asian bonytongue protein or transcript stable ID", 
          "Asian bonytongue chromosome/scaffold name", "Asian bonytongue chromosome/scaffold start (bp)", 
          "Asian bonytongue chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Asian bonytongue", "Asian bonytongue homology type", 
          "%id. target Asian bonytongue gene identical to query gene", 
          "%id. query gene identical to target Asian bonytongue gene", 
          "Asian bonytongue Gene-order conservation score", "Asian bonytongue Whole-genome alignment coverage", 
          "Asian bonytongue orthology confidence [0 low, 1 high]", 
          "Atlantic cod gene stable ID", "Atlantic cod gene name", 
          "Atlantic cod protein or transcript stable ID", "Atlantic cod chromosome/scaffold name", 
          "Atlantic cod chromosome/scaffold start (bp)", "Atlantic cod chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Atlantic cod", 
          "Atlantic cod homology type", "%id. target Atlantic cod gene identical to query gene", 
          "%id. query gene identical to target Atlantic cod gene", 
          "Atlantic cod Gene-order conservation score", "Atlantic cod orthology confidence [0 low, 1 high]", 
          "Atlantic herring gene stable ID", "Atlantic herring gene name", 
          "Atlantic herring protein or transcript stable ID", "Atlantic herring chromosome/scaffold name", 
          "Atlantic herring chromosome/scaffold start (bp)", "Atlantic herring chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Atlantic herring", 
          "Atlantic herring homology type", "%id. target Atlantic herring gene identical to query gene", 
          "%id. query gene identical to target Atlantic herring gene", 
          "Atlantic herring Gene-order conservation score", "Atlantic herring Whole-genome alignment coverage", 
          "Atlantic herring orthology confidence [0 low, 1 high]", 
          "Atlantic salmon gene stable ID", "Atlantic salmon gene name", 
          "Atlantic salmon protein or transcript stable ID", "Atlantic salmon chromosome/scaffold name", 
          "Atlantic salmon chromosome/scaffold start (bp)", "Atlantic salmon chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Atlantic salmon", 
          "Atlantic salmon homology type", "%id. target Atlantic salmon gene identical to query gene", 
          "%id. query gene identical to target Atlantic salmon gene", 
          "Atlantic salmon Gene-order conservation score", "Atlantic salmon Whole-genome alignment coverage", 
          "Atlantic salmon orthology confidence [0 low, 1 high]", 
          "Australian saltwater crocodile gene stable ID", "Australian saltwater crocodile gene name", 
          "Australian saltwater crocodile protein or transcript stable ID", 
          "Australian saltwater crocodile chromosome/scaffold name", 
          "Australian saltwater crocodile chromosome/scaffold start (bp)", 
          "Australian saltwater crocodile chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Australian saltwater crocodile", 
          "Australian saltwater crocodile homology type", "%id. target Australian saltwater crocodile gene identical to query gene", 
          "%id. query gene identical to target Australian saltwater crocodile gene", 
          "Australian saltwater crocodile Gene-order conservation score", 
          "Australian saltwater crocodile Whole-genome alignment coverage", 
          "Australian saltwater crocodile orthology confidence [0 low, 1 high]", 
          "Ballan wrasse gene stable ID", "Ballan wrasse gene name", 
          "Ballan wrasse protein or transcript stable ID", "Ballan wrasse chromosome/scaffold name", 
          "Ballan wrasse chromosome/scaffold start (bp)", "Ballan wrasse chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Ballan wrasse", 
          "Ballan wrasse homology type", "%id. target Ballan wrasse gene identical to query gene", 
          "%id. query gene identical to target Ballan wrasse gene", 
          "Ballan wrasse Gene-order conservation score", "Ballan wrasse Whole-genome alignment coverage", 
          "Ballan wrasse orthology confidence [0 low, 1 high]", 
          "Barramundi perch gene stable ID", "Barramundi perch gene name", 
          "Barramundi perch protein or transcript stable ID", "Barramundi perch chromosome/scaffold name", 
          "Barramundi perch chromosome/scaffold start (bp)", "Barramundi perch chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Barramundi perch", 
          "Barramundi perch homology type", "%id. target Barramundi perch gene identical to query gene", 
          "%id. query gene identical to target Barramundi perch gene", 
          "Barramundi perch Gene-order conservation score", "Barramundi perch Whole-genome alignment coverage", 
          "Barramundi perch orthology confidence [0 low, 1 high]", 
          "Beluga whale gene stable ID", "Beluga whale gene name", 
          "Beluga whale protein or transcript stable ID", "Beluga whale chromosome/scaffold name", 
          "Beluga whale chromosome/scaffold start (bp)", "Beluga whale chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Beluga whale", 
          "Beluga whale homology type", "%id. target Beluga whale gene identical to query gene", 
          "%id. query gene identical to target Beluga whale gene", 
          "Beluga whale Gene-order conservation score", "Beluga whale Whole-genome alignment coverage", 
          "Beluga whale orthology confidence [0 low, 1 high]", 
          "Bicolor damselfish gene stable ID", "Bicolor damselfish gene name", 
          "Bicolor damselfish protein or transcript stable ID", 
          "Bicolor damselfish chromosome/scaffold name", "Bicolor damselfish chromosome/scaffold start (bp)", 
          "Bicolor damselfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Bicolor damselfish", "Bicolor damselfish homology type", 
          "%id. target Bicolor damselfish gene identical to query gene", 
          "%id. query gene identical to target Bicolor damselfish gene", 
          "Bicolor damselfish Gene-order conservation score", "Bicolor damselfish Whole-genome alignment coverage", 
          "Bicolor damselfish orthology confidence [0 low, 1 high]", 
          "Black snub-nosed monkey gene stable ID", "Black snub-nosed monkey gene name", 
          "Black snub-nosed monkey protein or transcript stable ID", 
          "Black snub-nosed monkey chromosome/scaffold name", "Black snub-nosed monkey chromosome/scaffold start (bp)", 
          "Black snub-nosed monkey chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Black snub-nosed monkey", 
          "Black snub-nosed monkey homology type", "%id. target Black snub-nosed monkey gene identical to query gene", 
          "%id. query gene identical to target Black snub-nosed monkey gene", 
          "Black snub-nosed monkey Gene-order conservation score", 
          "Black snub-nosed monkey Whole-genome alignment coverage", 
          "Black snub-nosed monkey orthology confidence [0 low, 1 high]", 
          "Blue whale gene stable ID", "Blue whale gene name", 
          "Blue whale protein or transcript stable ID", "Blue whale chromosome/scaffold name", 
          "Blue whale chromosome/scaffold start (bp)", "Blue whale chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Blue whale", 
          "Blue whale homology type", "%id. target Blue whale gene identical to query gene", 
          "%id. query gene identical to target Blue whale gene", 
          "Blue whale Gene-order conservation score", "Blue whale Whole-genome alignment coverage", 
          "Blue whale orthology confidence [0 low, 1 high]", "Blue-ringed sea krait gene stable ID", 
          "Blue-ringed sea krait gene name", "Blue-ringed sea krait protein or transcript stable ID", 
          "Blue-ringed sea krait chromosome/scaffold name", "Blue-ringed sea krait chromosome/scaffold start (bp)", 
          "Blue-ringed sea krait chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Blue-ringed sea krait", 
          "Blue-ringed sea krait homology type", "%id. target Blue-ringed sea krait gene identical to query gene", 
          "%id. query gene identical to target Blue-ringed sea krait gene", 
          "Blue-ringed sea krait Gene-order conservation score", 
          "Blue-ringed sea krait Whole-genome alignment coverage", 
          "Blue-ringed sea krait orthology confidence [0 low, 1 high]", 
          "Bolivian squirrel monkey gene stable ID", "Bolivian squirrel monkey gene name", 
          "Bolivian squirrel monkey protein or transcript stable ID", 
          "Bolivian squirrel monkey chromosome/scaffold name", 
          "Bolivian squirrel monkey chromosome/scaffold start (bp)", 
          "Bolivian squirrel monkey chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Bolivian squirrel monkey", 
          "Bolivian squirrel monkey homology type", "%id. target Bolivian squirrel monkey gene identical to query gene", 
          "%id. query gene identical to target Bolivian squirrel monkey gene", 
          "Bolivian squirrel monkey Gene-order conservation score", 
          "Bolivian squirrel monkey Whole-genome alignment coverage", 
          "Bolivian squirrel monkey orthology confidence [0 low, 1 high]", 
          "Bonobo gene stable ID", "Bonobo gene name", "Bonobo protein or transcript stable ID", 
          "Bonobo chromosome/scaffold name", "Bonobo chromosome/scaffold start (bp)", 
          "Bonobo chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Bonobo", "Bonobo homology type", 
          "%id. target Bonobo gene identical to query gene", "%id. query gene identical to target Bonobo gene", 
          "Bonobo Gene-order conservation score", "Bonobo Whole-genome alignment coverage", 
          "Bonobo orthology confidence [0 low, 1 high]", "Brown trout gene stable ID", 
          "Brown trout gene name", "Brown trout protein or transcript stable ID", 
          "Brown trout chromosome/scaffold name", "Brown trout chromosome/scaffold start (bp)", 
          "Brown trout chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Brown trout", "Brown trout homology type", 
          "%id. target Brown trout gene identical to query gene", 
          "%id. query gene identical to target Brown trout gene", 
          "Brown trout Gene-order conservation score", "Brown trout Whole-genome alignment coverage", 
          "Brown trout orthology confidence [0 low, 1 high]", "Burton's mouthbrooder gene stable ID", 
          "Burton's mouthbrooder gene name", "Burton's mouthbrooder protein or transcript stable ID", 
          "Burton's mouthbrooder chromosome/scaffold name", "Burton's mouthbrooder chromosome/scaffold start (bp)", 
          "Burton's mouthbrooder chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Burton's mouthbrooder", 
          "Burton's mouthbrooder homology type", "%id. target Burton's mouthbrooder gene identical to query gene", 
          "%id. query gene identical to target Burton's mouthbrooder gene", 
          "Burton's mouthbrooder Gene-order conservation score", 
          "Burton's mouthbrooder Whole-genome alignment coverage", 
          "Burton's mouthbrooder orthology confidence [0 low, 1 high]", 
          "Bushbaby gene stable ID", "Bushbaby gene name", "Bushbaby protein or transcript stable ID", 
          "Bushbaby chromosome/scaffold name", "Bushbaby chromosome/scaffold start (bp)", 
          "Bushbaby chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Bushbaby", "Bushbaby homology type", 
          "%id. target Bushbaby gene identical to query gene", 
          "%id. query gene identical to target Bushbaby gene", 
          "Bushbaby Gene-order conservation score", "Bushbaby Whole-genome alignment coverage", 
          "Bushbaby orthology confidence [0 low, 1 high]", "C.intestinalis gene stable ID", 
          "C.intestinalis gene name", "C.intestinalis protein or transcript stable ID", 
          "C.intestinalis chromosome/scaffold name", "C.intestinalis chromosome/scaffold start (bp)", 
          "C.intestinalis chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with C.intestinalis", "C.intestinalis homology type", 
          "%id. target C.intestinalis gene identical to query gene", 
          "%id. query gene identical to target C.intestinalis gene", 
          "C.intestinalis Whole-genome alignment coverage", "C.intestinalis orthology confidence [0 low, 1 high]", 
          "C.savignyi gene stable ID", "C.savignyi gene name", 
          "C.savignyi protein or transcript stable ID", "C.savignyi chromosome/scaffold name", 
          "C.savignyi chromosome/scaffold start (bp)", "C.savignyi chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with C.savignyi", 
          "C.savignyi homology type", "%id. target C.savignyi gene identical to query gene", 
          "%id. query gene identical to target C.savignyi gene", 
          "C.savignyi Whole-genome alignment coverage", "C.savignyi orthology confidence [0 low, 1 high]", 
          "Caenorhabditis elegans gene stable ID", "Caenorhabditis elegans gene name", 
          "Caenorhabditis elegans protein or transcript stable ID", 
          "Caenorhabditis elegans chromosome/scaffold name", "Caenorhabditis elegans chromosome/scaffold start (bp)", 
          "Caenorhabditis elegans chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Caenorhabditis elegans", 
          "Caenorhabditis elegans homology type", "%id. target Caenorhabditis elegans gene identical to query gene", 
          "%id. query gene identical to target Caenorhabditis elegans gene", 
          "Caenorhabditis elegans orthology confidence [0 low, 1 high]", 
          "Capuchin gene stable ID", "Capuchin gene name", "Capuchin protein or transcript stable ID", 
          "Capuchin chromosome/scaffold name", "Capuchin chromosome/scaffold start (bp)", 
          "Capuchin chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Capuchin", "Capuchin homology type", 
          "%id. target Capuchin gene identical to query gene", 
          "%id. query gene identical to target Capuchin gene", 
          "Capuchin Gene-order conservation score", "Capuchin Whole-genome alignment coverage", 
          "Capuchin orthology confidence [0 low, 1 high]", "Cat gene stable ID", 
          "Cat gene name", "Cat protein or transcript stable ID", 
          "Cat chromosome/scaffold name", "Cat chromosome/scaffold start (bp)", 
          "Cat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Cat", "Cat homology type", 
          "%id. target Cat gene identical to query gene", "%id. query gene identical to target Cat gene", 
          "Cat Gene-order conservation score", "Cat Whole-genome alignment coverage", 
          "Cat orthology confidence [0 low, 1 high]", "Chacoan peccary gene stable ID", 
          "Chacoan peccary gene name", "Chacoan peccary protein or transcript stable ID", 
          "Chacoan peccary chromosome/scaffold name", "Chacoan peccary chromosome/scaffold start (bp)", 
          "Chacoan peccary chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Chacoan peccary", "Chacoan peccary homology type", 
          "%id. target Chacoan peccary gene identical to query gene", 
          "%id. query gene identical to target Chacoan peccary gene", 
          "Chacoan peccary Gene-order conservation score", "Chacoan peccary Whole-genome alignment coverage", 
          "Chacoan peccary orthology confidence [0 low, 1 high]", 
          "Channel bull blenny gene stable ID", "Channel bull blenny gene name", 
          "Channel bull blenny protein or transcript stable ID", 
          "Channel bull blenny chromosome/scaffold name", "Channel bull blenny chromosome/scaffold start (bp)", 
          "Channel bull blenny chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Channel bull blenny", "Channel bull blenny homology type", 
          "%id. target Channel bull blenny gene identical to query gene", 
          "%id. query gene identical to target Channel bull blenny gene", 
          "Channel bull blenny Gene-order conservation score", 
          "Channel bull blenny Whole-genome alignment coverage", 
          "Channel bull blenny orthology confidence [0 low, 1 high]", 
          "Channel catfish gene stable ID", "Channel catfish gene name", 
          "Channel catfish protein or transcript stable ID", "Channel catfish chromosome/scaffold name", 
          "Channel catfish chromosome/scaffold start (bp)", "Channel catfish chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Channel catfish", 
          "Channel catfish homology type", "%id. target Channel catfish gene identical to query gene", 
          "%id. query gene identical to target Channel catfish gene", 
          "Channel catfish Gene-order conservation score", "Channel catfish Whole-genome alignment coverage", 
          "Channel catfish orthology confidence [0 low, 1 high]", 
          "Chicken gene stable ID", "Chicken gene name", "Chicken protein or transcript stable ID", 
          "Chicken chromosome/scaffold name", "Chicken chromosome/scaffold start (bp)", 
          "Chicken chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Chicken", "Chicken homology type", 
          "%id. target Chicken gene identical to query gene", "%id. query gene identical to target Chicken gene", 
          "Chicken Gene-order conservation score", "Chicken Whole-genome alignment coverage", 
          "Chicken orthology confidence [0 low, 1 high]", "Chimpanzee gene stable ID", 
          "Chimpanzee gene name", "Chimpanzee protein or transcript stable ID", 
          "Chimpanzee chromosome/scaffold name", "Chimpanzee chromosome/scaffold start (bp)", 
          "Chimpanzee chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Chimpanzee", "Chimpanzee homology type", 
          "%id. target Chimpanzee gene identical to query gene", 
          "%id. query gene identical to target Chimpanzee gene", 
          "Chimpanzee Gene-order conservation score", "Chimpanzee Whole-genome alignment coverage", 
          "Chimpanzee orthology confidence [0 low, 1 high]", "Chinese hamster CHOK1GS gene stable ID", 
          "Chinese hamster CHOK1GS gene name", "Chinese hamster CHOK1GS protein or transcript stable ID", 
          "Chinese hamster CHOK1GS chromosome/scaffold name", "Chinese hamster CHOK1GS chromosome/scaffold start (bp)", 
          "Chinese hamster CHOK1GS chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Chinese hamster CHOK1GS", 
          "Chinese hamster CHOK1GS homology type", "%id. target Chinese hamster CHOK1GS gene identical to query gene", 
          "%id. query gene identical to target Chinese hamster CHOK1GS gene", 
          "Chinese hamster CHOK1GS Gene-order conservation score", 
          "Chinese hamster CHOK1GS Whole-genome alignment coverage", 
          "Chinese hamster CHOK1GS orthology confidence [0 low, 1 high]", 
          "Chinese medaka gene stable ID", "Chinese medaka gene name", 
          "Chinese medaka protein or transcript stable ID", "Chinese medaka chromosome/scaffold name", 
          "Chinese medaka chromosome/scaffold start (bp)", "Chinese medaka chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Chinese medaka", 
          "Chinese medaka homology type", "%id. target Chinese medaka gene identical to query gene", 
          "%id. query gene identical to target Chinese medaka gene", 
          "Chinese medaka Gene-order conservation score", "Chinese medaka Whole-genome alignment coverage", 
          "Chinese medaka orthology confidence [0 low, 1 high]", 
          "Chinese softshell turtle gene stable ID", "Chinese softshell turtle gene name", 
          "Chinese softshell turtle protein or transcript stable ID", 
          "Chinese softshell turtle chromosome/scaffold name", 
          "Chinese softshell turtle chromosome/scaffold start (bp)", 
          "Chinese softshell turtle chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Chinese softshell turtle", 
          "Chinese softshell turtle homology type", "%id. target Chinese softshell turtle gene identical to query gene", 
          "%id. query gene identical to target Chinese softshell turtle gene", 
          "Chinese softshell turtle Gene-order conservation score", 
          "Chinese softshell turtle Whole-genome alignment coverage", 
          "Chinese softshell turtle orthology confidence [0 low, 1 high]", 
          "Chinook salmon gene stable ID", "Chinook salmon gene name", 
          "Chinook salmon protein or transcript stable ID", "Chinook salmon chromosome/scaffold name", 
          "Chinook salmon chromosome/scaffold start (bp)", "Chinook salmon chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Chinook salmon", 
          "Chinook salmon homology type", "%id. target Chinook salmon gene identical to query gene", 
          "%id. query gene identical to target Chinook salmon gene", 
          "Chinook salmon Gene-order conservation score", "Chinook salmon Whole-genome alignment coverage", 
          "Chinook salmon orthology confidence [0 low, 1 high]", 
          "Climbing perch gene stable ID", "Climbing perch gene name", 
          "Climbing perch protein or transcript stable ID", "Climbing perch chromosome/scaffold name", 
          "Climbing perch chromosome/scaffold start (bp)", "Climbing perch chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Climbing perch", 
          "Climbing perch homology type", "%id. target Climbing perch gene identical to query gene", 
          "%id. query gene identical to target Climbing perch gene", 
          "Climbing perch Gene-order conservation score", "Climbing perch orthology confidence [0 low, 1 high]", 
          "Clown anemonefish gene stable ID", "Clown anemonefish gene name", 
          "Clown anemonefish protein or transcript stable ID", 
          "Clown anemonefish chromosome/scaffold name", "Clown anemonefish chromosome/scaffold start (bp)", 
          "Clown anemonefish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Clown anemonefish", "Clown anemonefish homology type", 
          "%id. target Clown anemonefish gene identical to query gene", 
          "%id. query gene identical to target Clown anemonefish gene", 
          "Clown anemonefish Gene-order conservation score", "Clown anemonefish Whole-genome alignment coverage", 
          "Clown anemonefish orthology confidence [0 low, 1 high]", 
          "Coelacanth gene stable ID", "Coelacanth gene name", 
          "Coelacanth protein or transcript stable ID", "Coelacanth chromosome/scaffold name", 
          "Coelacanth chromosome/scaffold start (bp)", "Coelacanth chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Coelacanth", 
          "Coelacanth homology type", "%id. target Coelacanth gene identical to query gene", 
          "%id. query gene identical to target Coelacanth gene", 
          "Coelacanth Gene-order conservation score", "Coelacanth Whole-genome alignment coverage", 
          "Coelacanth orthology confidence [0 low, 1 high]", "Coho salmon gene stable ID", 
          "Coho salmon gene name", "Coho salmon protein or transcript stable ID", 
          "Coho salmon chromosome/scaffold name", "Coho salmon chromosome/scaffold start (bp)", 
          "Coho salmon chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Coho salmon", "Coho salmon homology type", 
          "%id. target Coho salmon gene identical to query gene", 
          "%id. query gene identical to target Coho salmon gene", 
          "Coho salmon Gene-order conservation score", "Coho salmon Whole-genome alignment coverage", 
          "Coho salmon orthology confidence [0 low, 1 high]", "Collared flycatcher gene stable ID", 
          "Collared flycatcher gene name", "Collared flycatcher protein or transcript stable ID", 
          "Collared flycatcher chromosome/scaffold name", "Collared flycatcher chromosome/scaffold start (bp)", 
          "Collared flycatcher chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Collared flycatcher", "Collared flycatcher homology type", 
          "%id. target Collared flycatcher gene identical to query gene", 
          "%id. query gene identical to target Collared flycatcher gene", 
          "Collared flycatcher Gene-order conservation score", 
          "Collared flycatcher orthology confidence [0 low, 1 high]", 
          "Common canary gene stable ID", "Common canary gene name", 
          "Common canary protein or transcript stable ID", "Common canary chromosome/scaffold name", 
          "Common canary chromosome/scaffold start (bp)", "Common canary chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Common canary", 
          "Common canary homology type", "%id. target Common canary gene identical to query gene", 
          "%id. query gene identical to target Common canary gene", 
          "Common canary Gene-order conservation score", "Common canary Whole-genome alignment coverage", 
          "Common canary orthology confidence [0 low, 1 high]", 
          "Common carp gene stable ID", "Common carp gene name", 
          "Common carp protein or transcript stable ID", "Common carp chromosome/scaffold name", 
          "Common carp chromosome/scaffold start (bp)", "Common carp chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Common carp", 
          "Common carp homology type", "%id. target Common carp gene identical to query gene", 
          "%id. query gene identical to target Common carp gene", 
          "Common carp Gene-order conservation score", "Common carp Whole-genome alignment coverage", 
          "Common carp orthology confidence [0 low, 1 high]", "Common wall lizard gene stable ID", 
          "Common wall lizard gene name", "Common wall lizard protein or transcript stable ID", 
          "Common wall lizard chromosome/scaffold name", "Common wall lizard chromosome/scaffold start (bp)", 
          "Common wall lizard chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Common wall lizard", "Common wall lizard homology type", 
          "%id. target Common wall lizard gene identical to query gene", 
          "%id. query gene identical to target Common wall lizard gene", 
          "Common wall lizard Gene-order conservation score", "Common wall lizard Whole-genome alignment coverage", 
          "Common wall lizard orthology confidence [0 low, 1 high]", 
          "Common wombat gene stable ID", "Common wombat gene name", 
          "Common wombat protein or transcript stable ID", "Common wombat chromosome/scaffold name", 
          "Common wombat chromosome/scaffold start (bp)", "Common wombat chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Common wombat", 
          "Common wombat homology type", "%id. target Common wombat gene identical to query gene", 
          "%id. query gene identical to target Common wombat gene", 
          "Common wombat Gene-order conservation score", "Common wombat Whole-genome alignment coverage", 
          "Common wombat orthology confidence [0 low, 1 high]", 
          "Coquerel's sifaka gene stable ID", "Coquerel's sifaka gene name", 
          "Coquerel's sifaka protein or transcript stable ID", 
          "Coquerel's sifaka chromosome/scaffold name", "Coquerel's sifaka chromosome/scaffold start (bp)", 
          "Coquerel's sifaka chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Coquerel's sifaka", "Coquerel's sifaka homology type", 
          "%id. target Coquerel's sifaka gene identical to query gene", 
          "%id. query gene identical to target Coquerel's sifaka gene", 
          "Coquerel's sifaka Gene-order conservation score", "Coquerel's sifaka Whole-genome alignment coverage", 
          "Coquerel's sifaka orthology confidence [0 low, 1 high]", 
          "Cow gene stable ID", "Cow gene name", "Cow protein or transcript stable ID", 
          "Cow chromosome/scaffold name", "Cow chromosome/scaffold start (bp)", 
          "Cow chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Cow", "Cow homology type", 
          "%id. target Cow gene identical to query gene", "%id. query gene identical to target Cow gene", 
          "Cow Gene-order conservation score", "Cow Whole-genome alignment coverage", 
          "Cow orthology confidence [0 low, 1 high]", "Crab-eating macaque gene stable ID", 
          "Crab-eating macaque gene name", "Crab-eating macaque protein or transcript stable ID", 
          "Crab-eating macaque chromosome/scaffold name", "Crab-eating macaque chromosome/scaffold start (bp)", 
          "Crab-eating macaque chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Crab-eating macaque", "Crab-eating macaque homology type", 
          "%id. target Crab-eating macaque gene identical to query gene", 
          "%id. query gene identical to target Crab-eating macaque gene", 
          "Crab-eating macaque Gene-order conservation score", 
          "Crab-eating macaque Whole-genome alignment coverage", 
          "Crab-eating macaque orthology confidence [0 low, 1 high]", 
          "Degu gene stable ID", "Degu gene name", "Degu protein or transcript stable ID", 
          "Degu chromosome/scaffold name", "Degu chromosome/scaffold start (bp)", 
          "Degu chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Degu", "Degu homology type", 
          "%id. target Degu gene identical to query gene", "%id. query gene identical to target Degu gene", 
          "Degu Gene-order conservation score", "Degu Whole-genome alignment coverage", 
          "Degu orthology confidence [0 low, 1 high]", "Denticle herring gene stable ID", 
          "Denticle herring gene name", "Denticle herring protein or transcript stable ID", 
          "Denticle herring chromosome/scaffold name", "Denticle herring chromosome/scaffold start (bp)", 
          "Denticle herring chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Denticle herring", "Denticle herring homology type", 
          "%id. target Denticle herring gene identical to query gene", 
          "%id. query gene identical to target Denticle herring gene", 
          "Denticle herring Gene-order conservation score", "Denticle herring Whole-genome alignment coverage", 
          "Denticle herring orthology confidence [0 low, 1 high]", 
          "Dingo gene stable ID", "Dingo gene name", "Dingo protein or transcript stable ID", 
          "Dingo chromosome/scaffold name", "Dingo chromosome/scaffold start (bp)", 
          "Dingo chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Dingo", "Dingo homology type", 
          "%id. target Dingo gene identical to query gene", "%id. query gene identical to target Dingo gene", 
          "Dingo Gene-order conservation score", "Dingo Whole-genome alignment coverage", 
          "Dingo orthology confidence [0 low, 1 high]", "Dog gene stable ID", 
          "Dog gene name", "Dog protein or transcript stable ID", 
          "Dog chromosome/scaffold name", "Dog chromosome/scaffold start (bp)", 
          "Dog chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Dog", "Dog homology type", 
          "%id. target Dog gene identical to query gene", "%id. query gene identical to target Dog gene", 
          "Dog Gene-order conservation score", "Dog Whole-genome alignment coverage", 
          "Dog orthology confidence [0 low, 1 high]", "Dolphin gene stable ID", 
          "Dolphin gene name", "Dolphin protein or transcript stable ID", 
          "Dolphin chromosome/scaffold name", "Dolphin chromosome/scaffold start (bp)", 
          "Dolphin chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Dolphin", "Dolphin homology type", 
          "%id. target Dolphin gene identical to query gene", "%id. query gene identical to target Dolphin gene", 
          "Dolphin Gene-order conservation score", "Dolphin Whole-genome alignment coverage", 
          "Dolphin orthology confidence [0 low, 1 high]", "Domestic yak gene stable ID", 
          "Domestic yak gene name", "Domestic yak protein or transcript stable ID", 
          "Domestic yak chromosome/scaffold name", "Domestic yak chromosome/scaffold start (bp)", 
          "Domestic yak chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Domestic yak", "Domestic yak homology type", 
          "%id. target Domestic yak gene identical to query gene", 
          "%id. query gene identical to target Domestic yak gene", 
          "Domestic yak Gene-order conservation score", "Domestic yak Whole-genome alignment coverage", 
          "Domestic yak orthology confidence [0 low, 1 high]", 
          "Donkey gene stable ID", "Donkey gene name", "Donkey protein or transcript stable ID", 
          "Donkey chromosome/scaffold name", "Donkey chromosome/scaffold start (bp)", 
          "Donkey chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Donkey", "Donkey homology type", 
          "%id. target Donkey gene identical to query gene", "%id. query gene identical to target Donkey gene", 
          "Donkey Gene-order conservation score", "Donkey Whole-genome alignment coverage", 
          "Donkey orthology confidence [0 low, 1 high]", "Drill gene stable ID", 
          "Drill gene name", "Drill protein or transcript stable ID", 
          "Drill chromosome/scaffold name", "Drill chromosome/scaffold start (bp)", 
          "Drill chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Drill", "Drill homology type", 
          "%id. target Drill gene identical to query gene", "%id. query gene identical to target Drill gene", 
          "Drill Gene-order conservation score", "Drill Whole-genome alignment coverage", 
          "Drill orthology confidence [0 low, 1 high]", "Drosophila melanogaster gene stable ID", 
          "Drosophila melanogaster gene name", "Drosophila melanogaster protein or transcript stable ID", 
          "Drosophila melanogaster chromosome/scaffold name", "Drosophila melanogaster chromosome/scaffold start (bp)", 
          "Drosophila melanogaster chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Drosophila melanogaster", 
          "Drosophila melanogaster homology type", "%id. target Drosophila melanogaster gene identical to query gene", 
          "%id. query gene identical to target Drosophila melanogaster gene", 
          "Drosophila melanogaster orthology confidence [0 low, 1 high]", 
          "Duck gene stable ID", "Duck gene name", "Duck protein or transcript stable ID", 
          "Duck chromosome/scaffold name", "Duck chromosome/scaffold start (bp)", 
          "Duck chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Duck", "Duck homology type", 
          "%id. target Duck gene identical to query gene", "%id. query gene identical to target Duck gene", 
          "Duck Gene-order conservation score", "Duck Whole-genome alignment coverage", 
          "Duck orthology confidence [0 low, 1 high]", "Eastern brown snake gene stable ID", 
          "Eastern brown snake gene name", "Eastern brown snake protein or transcript stable ID", 
          "Eastern brown snake chromosome/scaffold name", "Eastern brown snake chromosome/scaffold start (bp)", 
          "Eastern brown snake chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Eastern brown snake", "Eastern brown snake homology type", 
          "%id. target Eastern brown snake gene identical to query gene", 
          "%id. query gene identical to target Eastern brown snake gene", 
          "Eastern brown snake Gene-order conservation score", 
          "Eastern brown snake Whole-genome alignment coverage", 
          "Eastern brown snake orthology confidence [0 low, 1 high]", 
          "Eastern happy gene stable ID", "Eastern happy gene name", 
          "Eastern happy protein or transcript stable ID", "Eastern happy chromosome/scaffold name", 
          "Eastern happy chromosome/scaffold start (bp)", "Eastern happy chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Eastern happy", 
          "Eastern happy homology type", "%id. target Eastern happy gene identical to query gene", 
          "%id. query gene identical to target Eastern happy gene", 
          "Eastern happy Gene-order conservation score", "Eastern happy Whole-genome alignment coverage", 
          "Eastern happy orthology confidence [0 low, 1 high]", 
          "Electric eel gene stable ID", "Electric eel gene name", 
          "Electric eel protein or transcript stable ID", "Electric eel chromosome/scaffold name", 
          "Electric eel chromosome/scaffold start (bp)", "Electric eel chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Electric eel", 
          "Electric eel homology type", "%id. target Electric eel gene identical to query gene", 
          "%id. query gene identical to target Electric eel gene", 
          "Electric eel Gene-order conservation score", "Electric eel Whole-genome alignment coverage", 
          "Electric eel orthology confidence [0 low, 1 high]", 
          "Elephant gene stable ID", "Elephant gene name", "Elephant protein or transcript stable ID", 
          "Elephant chromosome/scaffold name", "Elephant chromosome/scaffold start (bp)", 
          "Elephant chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Elephant", "Elephant homology type", 
          "%id. target Elephant gene identical to query gene", 
          "%id. query gene identical to target Elephant gene", 
          "Elephant Gene-order conservation score", "Elephant Whole-genome alignment coverage", 
          "Elephant orthology confidence [0 low, 1 high]", "Elephant shark gene stable ID", 
          "Elephant shark gene name", "Elephant shark protein or transcript stable ID", 
          "Elephant shark chromosome/scaffold name", "Elephant shark chromosome/scaffold start (bp)", 
          "Elephant shark chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Elephant shark", "Elephant shark homology type", 
          "%id. target Elephant shark gene identical to query gene", 
          "%id. query gene identical to target Elephant shark gene", 
          "Elephant shark Whole-genome alignment coverage", "Elephant shark orthology confidence [0 low, 1 high]", 
          "Eurasian red squirrel gene stable ID", "Eurasian red squirrel gene name", 
          "Eurasian red squirrel protein or transcript stable ID", 
          "Eurasian red squirrel chromosome/scaffold name", "Eurasian red squirrel chromosome/scaffold start (bp)", 
          "Eurasian red squirrel chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Eurasian red squirrel", 
          "Eurasian red squirrel homology type", "%id. target Eurasian red squirrel gene identical to query gene", 
          "%id. query gene identical to target Eurasian red squirrel gene", 
          "Eurasian red squirrel Gene-order conservation score", 
          "Eurasian red squirrel Whole-genome alignment coverage", 
          "Eurasian red squirrel orthology confidence [0 low, 1 high]", 
          "European seabass gene stable ID", "European seabass gene name", 
          "European seabass protein or transcript stable ID", "European seabass chromosome/scaffold name", 
          "European seabass chromosome/scaffold start (bp)", "European seabass chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with European seabass", 
          "European seabass homology type", "%id. target European seabass gene identical to query gene", 
          "%id. query gene identical to target European seabass gene", 
          "European seabass Gene-order conservation score", "European seabass Whole-genome alignment coverage", 
          "European seabass orthology confidence [0 low, 1 high]", 
          "Ferret gene stable ID", "Ferret gene name", "Ferret protein or transcript stable ID", 
          "Ferret chromosome/scaffold name", "Ferret chromosome/scaffold start (bp)", 
          "Ferret chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Ferret", "Ferret homology type", 
          "%id. target Ferret gene identical to query gene", "%id. query gene identical to target Ferret gene", 
          "Ferret Gene-order conservation score", "Ferret Whole-genome alignment coverage", 
          "Ferret orthology confidence [0 low, 1 high]", "Fugu gene stable ID", 
          "Fugu gene name", "Fugu protein or transcript stable ID", 
          "Fugu chromosome/scaffold name", "Fugu chromosome/scaffold start (bp)", 
          "Fugu chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Fugu", "Fugu homology type", 
          "%id. target Fugu gene identical to query gene", "%id. query gene identical to target Fugu gene", 
          "Fugu Gene-order conservation score", "Fugu Whole-genome alignment coverage", 
          "Fugu orthology confidence [0 low, 1 high]", "Giant panda gene stable ID", 
          "Giant panda gene name", "Giant panda protein or transcript stable ID", 
          "Giant panda chromosome/scaffold name", "Giant panda chromosome/scaffold start (bp)", 
          "Giant panda chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Giant panda", "Giant panda homology type", 
          "%id. target Giant panda gene identical to query gene", 
          "%id. query gene identical to target Giant panda gene", 
          "Giant panda Gene-order conservation score", "Giant panda orthology confidence [0 low, 1 high]", 
          "Gibbon gene stable ID", "Gibbon gene name", "Gibbon protein or transcript stable ID", 
          "Gibbon chromosome/scaffold name", "Gibbon chromosome/scaffold start (bp)", 
          "Gibbon chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Gibbon", "Gibbon homology type", 
          "%id. target Gibbon gene identical to query gene", "%id. query gene identical to target Gibbon gene", 
          "Gibbon Gene-order conservation score", "Gibbon Whole-genome alignment coverage", 
          "Gibbon orthology confidence [0 low, 1 high]", "Gilthead seabream gene stable ID", 
          "Gilthead seabream gene name", "Gilthead seabream protein or transcript stable ID", 
          "Gilthead seabream chromosome/scaffold name", "Gilthead seabream chromosome/scaffold start (bp)", 
          "Gilthead seabream chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Gilthead seabream", "Gilthead seabream homology type", 
          "%id. target Gilthead seabream gene identical to query gene", 
          "%id. query gene identical to target Gilthead seabream gene", 
          "Gilthead seabream Gene-order conservation score", "Gilthead seabream Whole-genome alignment coverage", 
          "Gilthead seabream orthology confidence [0 low, 1 high]", 
          "Goat gene stable ID", "Goat gene name", "Goat protein or transcript stable ID", 
          "Goat chromosome/scaffold name", "Goat chromosome/scaffold start (bp)", 
          "Goat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Goat", "Goat homology type", 
          "%id. target Goat gene identical to query gene", "%id. query gene identical to target Goat gene", 
          "Goat Gene-order conservation score", "Goat Whole-genome alignment coverage", 
          "Goat orthology confidence [0 low, 1 high]", "Golden Hamster gene stable ID", 
          "Golden Hamster gene name", "Golden Hamster protein or transcript stable ID", 
          "Golden Hamster chromosome/scaffold name", "Golden Hamster chromosome/scaffold start (bp)", 
          "Golden Hamster chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Golden Hamster", "Golden Hamster homology type", 
          "%id. target Golden Hamster gene identical to query gene", 
          "%id. query gene identical to target Golden Hamster gene", 
          "Golden Hamster Gene-order conservation score", "Golden Hamster Whole-genome alignment coverage", 
          "Golden Hamster orthology confidence [0 low, 1 high]", 
          "Golden eagle gene stable ID", "Golden eagle gene name", 
          "Golden eagle protein or transcript stable ID", "Golden eagle chromosome/scaffold name", 
          "Golden eagle chromosome/scaffold start (bp)", "Golden eagle chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Golden eagle", 
          "Golden eagle homology type", "%id. target Golden eagle gene identical to query gene", 
          "%id. query gene identical to target Golden eagle gene", 
          "Golden eagle Gene-order conservation score", "Golden eagle Whole-genome alignment coverage", 
          "Golden eagle orthology confidence [0 low, 1 high]", 
          "Golden snub-nosed monkey gene stable ID", "Golden snub-nosed monkey gene name", 
          "Golden snub-nosed monkey protein or transcript stable ID", 
          "Golden snub-nosed monkey chromosome/scaffold name", 
          "Golden snub-nosed monkey chromosome/scaffold start (bp)", 
          "Golden snub-nosed monkey chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Golden snub-nosed monkey", 
          "Golden snub-nosed monkey homology type", "%id. target Golden snub-nosed monkey gene identical to query gene", 
          "%id. query gene identical to target Golden snub-nosed monkey gene", 
          "Golden snub-nosed monkey Gene-order conservation score", 
          "Golden snub-nosed monkey Whole-genome alignment coverage", 
          "Golden snub-nosed monkey orthology confidence [0 low, 1 high]", 
          "Golden-line barbel gene stable ID", "Golden-line barbel gene name", 
          "Golden-line barbel protein or transcript stable ID", 
          "Golden-line barbel chromosome/scaffold name", "Golden-line barbel chromosome/scaffold start (bp)", 
          "Golden-line barbel chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Golden-line barbel", "Golden-line barbel homology type", 
          "%id. target Golden-line barbel gene identical to query gene", 
          "%id. query gene identical to target Golden-line barbel gene", 
          "Golden-line barbel Gene-order conservation score", "Golden-line barbel Whole-genome alignment coverage", 
          "Golden-line barbel orthology confidence [0 low, 1 high]", 
          "Goldfish gene stable ID", "Goldfish gene name", "Goldfish protein or transcript stable ID", 
          "Goldfish chromosome/scaffold name", "Goldfish chromosome/scaffold start (bp)", 
          "Goldfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Goldfish", "Goldfish homology type", 
          "%id. target Goldfish gene identical to query gene", 
          "%id. query gene identical to target Goldfish gene", 
          "Goldfish Gene-order conservation score", "Goldfish Whole-genome alignment coverage", 
          "Goldfish orthology confidence [0 low, 1 high]", "Goodes thornscrub tortoise gene stable ID", 
          "Goodes thornscrub tortoise gene name", "Goodes thornscrub tortoise protein or transcript stable ID", 
          "Goodes thornscrub tortoise chromosome/scaffold name", 
          "Goodes thornscrub tortoise chromosome/scaffold start (bp)", 
          "Goodes thornscrub tortoise chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Goodes thornscrub tortoise", 
          "Goodes thornscrub tortoise homology type", "%id. target Goodes thornscrub tortoise gene identical to query gene", 
          "%id. query gene identical to target Goodes thornscrub tortoise gene", 
          "Goodes thornscrub tortoise Gene-order conservation score", 
          "Goodes thornscrub tortoise Whole-genome alignment coverage", 
          "Goodes thornscrub tortoise orthology confidence [0 low, 1 high]", 
          "Gorilla gene stable ID", "Gorilla gene name", "Gorilla protein or transcript stable ID", 
          "Gorilla chromosome/scaffold name", "Gorilla chromosome/scaffold start (bp)", 
          "Gorilla chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Gorilla", "Gorilla homology type", 
          "%id. target Gorilla gene identical to query gene", "%id. query gene identical to target Gorilla gene", 
          "Gorilla Gene-order conservation score", "Gorilla Whole-genome alignment coverage", 
          "Gorilla orthology confidence [0 low, 1 high]", "Great Tit gene stable ID", 
          "Great Tit gene name", "Great Tit protein or transcript stable ID", 
          "Great Tit chromosome/scaffold name", "Great Tit chromosome/scaffold start (bp)", 
          "Great Tit chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Great Tit", "Great Tit homology type", 
          "%id. target Great Tit gene identical to query gene", 
          "%id. query gene identical to target Great Tit gene", 
          "Great Tit Gene-order conservation score", "Great Tit Whole-genome alignment coverage", 
          "Great Tit orthology confidence [0 low, 1 high]", "Greater amberjack gene stable ID", 
          "Greater amberjack gene name", "Greater amberjack protein or transcript stable ID", 
          "Greater amberjack chromosome/scaffold name", "Greater amberjack chromosome/scaffold start (bp)", 
          "Greater amberjack chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Greater amberjack", "Greater amberjack homology type", 
          "%id. target Greater amberjack gene identical to query gene", 
          "%id. query gene identical to target Greater amberjack gene", 
          "Greater amberjack Gene-order conservation score", "Greater amberjack Whole-genome alignment coverage", 
          "Greater amberjack orthology confidence [0 low, 1 high]", 
          "Greater bamboo lemur gene stable ID", "Greater bamboo lemur gene name", 
          "Greater bamboo lemur protein or transcript stable ID", 
          "Greater bamboo lemur chromosome/scaffold name", "Greater bamboo lemur chromosome/scaffold start (bp)", 
          "Greater bamboo lemur chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Greater bamboo lemur", 
          "Greater bamboo lemur homology type", "%id. target Greater bamboo lemur gene identical to query gene", 
          "%id. query gene identical to target Greater bamboo lemur gene", 
          "Greater bamboo lemur Gene-order conservation score", 
          "Greater bamboo lemur Whole-genome alignment coverage", 
          "Greater bamboo lemur orthology confidence [0 low, 1 high]", 
          "Greater horseshoe bat gene stable ID", "Greater horseshoe bat gene name", 
          "Greater horseshoe bat protein or transcript stable ID", 
          "Greater horseshoe bat chromosome/scaffold name", "Greater horseshoe bat chromosome/scaffold start (bp)", 
          "Greater horseshoe bat chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Greater horseshoe bat", 
          "Greater horseshoe bat homology type", "%id. target Greater horseshoe bat gene identical to query gene", 
          "%id. query gene identical to target Greater horseshoe bat gene", 
          "Greater horseshoe bat Gene-order conservation score", 
          "Greater horseshoe bat Whole-genome alignment coverage", 
          "Greater horseshoe bat orthology confidence [0 low, 1 high]", 
          "Green anole gene stable ID", "Green anole gene name", 
          "Green anole protein or transcript stable ID", "Green anole chromosome/scaffold name", 
          "Green anole chromosome/scaffold start (bp)", "Green anole chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Green anole", 
          "Green anole homology type", "%id. target Green anole gene identical to query gene", 
          "%id. query gene identical to target Green anole gene", 
          "Green anole Gene-order conservation score", "Green anole orthology confidence [0 low, 1 high]", 
          "Guinea Pig gene stable ID", "Guinea Pig gene name", 
          "Guinea Pig protein or transcript stable ID", "Guinea Pig chromosome/scaffold name", 
          "Guinea Pig chromosome/scaffold start (bp)", "Guinea Pig chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Guinea Pig", 
          "Guinea Pig homology type", "%id. target Guinea Pig gene identical to query gene", 
          "%id. query gene identical to target Guinea Pig gene", 
          "Guinea Pig Gene-order conservation score", "Guinea Pig Whole-genome alignment coverage", 
          "Guinea Pig orthology confidence [0 low, 1 high]", "Guppy gene stable ID", 
          "Guppy gene name", "Guppy protein or transcript stable ID", 
          "Guppy chromosome/scaffold name", "Guppy chromosome/scaffold start (bp)", 
          "Guppy chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Guppy", "Guppy homology type", 
          "%id. target Guppy gene identical to query gene", "%id. query gene identical to target Guppy gene", 
          "Guppy Gene-order conservation score", "Guppy Whole-genome alignment coverage", 
          "Guppy orthology confidence [0 low, 1 high]", "Hagfish gene stable ID", 
          "Hagfish gene name", "Hagfish protein or transcript stable ID", 
          "Hagfish chromosome/scaffold name", "Hagfish chromosome/scaffold start (bp)", 
          "Hagfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Hagfish", "Hagfish homology type", 
          "%id. target Hagfish gene identical to query gene", "%id. query gene identical to target Hagfish gene", 
          "Hagfish Whole-genome alignment coverage", "Hagfish orthology confidence [0 low, 1 high]", 
          "Hedgehog gene stable ID", "Hedgehog gene name", "Hedgehog protein or transcript stable ID", 
          "Hedgehog chromosome/scaffold name", "Hedgehog chromosome/scaffold start (bp)", 
          "Hedgehog chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Hedgehog", "Hedgehog homology type", 
          "%id. target Hedgehog gene identical to query gene", 
          "%id. query gene identical to target Hedgehog gene", 
          "Hedgehog Gene-order conservation score", "Hedgehog Whole-genome alignment coverage", 
          "Hedgehog orthology confidence [0 low, 1 high]", "Horse gene stable ID", 
          "Horse gene name", "Horse protein or transcript stable ID", 
          "Horse chromosome/scaffold name", "Horse chromosome/scaffold start (bp)", 
          "Horse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Horse", "Horse homology type", 
          "%id. target Horse gene identical to query gene", "%id. query gene identical to target Horse gene", 
          "Horse Gene-order conservation score", "Horse Whole-genome alignment coverage", 
          "Horse orthology confidence [0 low, 1 high]", "Huchen gene stable ID", 
          "Huchen gene name", "Huchen protein or transcript stable ID", 
          "Huchen chromosome/scaffold name", "Huchen chromosome/scaffold start (bp)", 
          "Huchen chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Huchen", "Huchen homology type", 
          "%id. target Huchen gene identical to query gene", "%id. query gene identical to target Huchen gene", 
          "Huchen Gene-order conservation score", "Huchen Whole-genome alignment coverage", 
          "Huchen orthology confidence [0 low, 1 high]", "Hybrid - Bos Indicus gene stable ID", 
          "Hybrid - Bos Indicus gene name", "Hybrid - Bos Indicus protein or transcript stable ID", 
          "Hybrid - Bos Indicus chromosome/scaffold name", "Hybrid - Bos Indicus chromosome/scaffold start (bp)", 
          "Hybrid - Bos Indicus chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Hybrid - Bos Indicus", 
          "Hybrid - Bos Indicus homology type", "%id. target Hybrid - Bos Indicus gene identical to query gene", 
          "%id. query gene identical to target Hybrid - Bos Indicus gene", 
          "Hybrid - Bos Indicus Gene-order conservation score", 
          "Hybrid - Bos Indicus Whole-genome alignment coverage", 
          "Hybrid - Bos Indicus orthology confidence [0 low, 1 high]", 
          "Hyrax gene stable ID", "Hyrax gene name", "Hyrax protein or transcript stable ID", 
          "Hyrax chromosome/scaffold name", "Hyrax chromosome/scaffold start (bp)", 
          "Hyrax chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Hyrax", "Hyrax homology type", 
          "%id. target Hyrax gene identical to query gene", "%id. query gene identical to target Hyrax gene", 
          "Hyrax Gene-order conservation score", "Hyrax Whole-genome alignment coverage", 
          "Hyrax orthology confidence [0 low, 1 high]", "Indian cobra gene stable ID", 
          "Indian cobra gene name", "Indian cobra protein or transcript stable ID", 
          "Indian cobra chromosome/scaffold name", "Indian cobra chromosome/scaffold start (bp)", 
          "Indian cobra chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Indian cobra", "Indian cobra homology type", 
          "%id. target Indian cobra gene identical to query gene", 
          "%id. query gene identical to target Indian cobra gene", 
          "Indian cobra Gene-order conservation score", "Indian cobra Whole-genome alignment coverage", 
          "Indian cobra orthology confidence [0 low, 1 high]", 
          "Indian medaka gene stable ID", "Indian medaka gene name", 
          "Indian medaka protein or transcript stable ID", "Indian medaka chromosome/scaffold name", 
          "Indian medaka chromosome/scaffold start (bp)", "Indian medaka chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Indian medaka", 
          "Indian medaka homology type", "%id. target Indian medaka gene identical to query gene", 
          "%id. query gene identical to target Indian medaka gene", 
          "Indian medaka Gene-order conservation score", "Indian medaka Whole-genome alignment coverage", 
          "Indian medaka orthology confidence [0 low, 1 high]", 
          "Japanese medaka HdrR gene stable ID", "Japanese medaka HdrR gene name", 
          "Japanese medaka HdrR protein or transcript stable ID", 
          "Japanese medaka HdrR chromosome/scaffold name", "Japanese medaka HdrR chromosome/scaffold start (bp)", 
          "Japanese medaka HdrR chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Japanese medaka HdrR", 
          "Japanese medaka HdrR homology type", "%id. target Japanese medaka HdrR gene identical to query gene", 
          "%id. query gene identical to target Japanese medaka HdrR gene", 
          "Japanese medaka HdrR Gene-order conservation score", 
          "Japanese medaka HdrR Whole-genome alignment coverage", 
          "Japanese medaka HdrR orthology confidence [0 low, 1 high]", 
          "Japanese quail gene stable ID", "Japanese quail gene name", 
          "Japanese quail protein or transcript stable ID", "Japanese quail chromosome/scaffold name", 
          "Japanese quail chromosome/scaffold start (bp)", "Japanese quail chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Japanese quail", 
          "Japanese quail homology type", "%id. target Japanese quail gene identical to query gene", 
          "%id. query gene identical to target Japanese quail gene", 
          "Japanese quail Gene-order conservation score", "Japanese quail Whole-genome alignment coverage", 
          "Japanese quail orthology confidence [0 low, 1 high]", 
          "Javanese ricefish gene stable ID", "Javanese ricefish gene name", 
          "Javanese ricefish protein or transcript stable ID", 
          "Javanese ricefish chromosome/scaffold name", "Javanese ricefish chromosome/scaffold start (bp)", 
          "Javanese ricefish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Javanese ricefish", "Javanese ricefish homology type", 
          "%id. target Javanese ricefish gene identical to query gene", 
          "%id. query gene identical to target Javanese ricefish gene", 
          "Javanese ricefish Gene-order conservation score", "Javanese ricefish Whole-genome alignment coverage", 
          "Javanese ricefish orthology confidence [0 low, 1 high]", 
          "Kakapo gene stable ID", "Kakapo gene name", "Kakapo protein or transcript stable ID", 
          "Kakapo chromosome/scaffold name", "Kakapo chromosome/scaffold start (bp)", 
          "Kakapo chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Kakapo", "Kakapo homology type", 
          "%id. target Kakapo gene identical to query gene", "%id. query gene identical to target Kakapo gene", 
          "Kakapo Gene-order conservation score", "Kakapo Whole-genome alignment coverage", 
          "Kakapo orthology confidence [0 low, 1 high]", "Kangaroo rat gene stable ID", 
          "Kangaroo rat gene name", "Kangaroo rat protein or transcript stable ID", 
          "Kangaroo rat chromosome/scaffold name", "Kangaroo rat chromosome/scaffold start (bp)", 
          "Kangaroo rat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Kangaroo rat", "Kangaroo rat homology type", 
          "%id. target Kangaroo rat gene identical to query gene", 
          "%id. query gene identical to target Kangaroo rat gene", 
          "Kangaroo rat Gene-order conservation score", "Kangaroo rat Whole-genome alignment coverage", 
          "Kangaroo rat orthology confidence [0 low, 1 high]", 
          "Koala gene stable ID", "Koala gene name", "Koala protein or transcript stable ID", 
          "Koala chromosome/scaffold name", "Koala chromosome/scaffold start (bp)", 
          "Koala chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Koala", "Koala homology type", 
          "%id. target Koala gene identical to query gene", "%id. query gene identical to target Koala gene", 
          "Koala Gene-order conservation score", "Koala Whole-genome alignment coverage", 
          "Koala orthology confidence [0 low, 1 high]", "Lamprey gene stable ID", 
          "Lamprey gene name", "Lamprey protein or transcript stable ID", 
          "Lamprey chromosome/scaffold name", "Lamprey chromosome/scaffold start (bp)", 
          "Lamprey chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Lamprey", "Lamprey homology type", 
          "%id. target Lamprey gene identical to query gene", "%id. query gene identical to target Lamprey gene", 
          "Lamprey Whole-genome alignment coverage", "Lamprey orthology confidence [0 low, 1 high]", 
          "Large yellow croaker gene stable ID", "Large yellow croaker gene name", 
          "Large yellow croaker protein or transcript stable ID", 
          "Large yellow croaker chromosome/scaffold name", "Large yellow croaker chromosome/scaffold start (bp)", 
          "Large yellow croaker chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Large yellow croaker", 
          "Large yellow croaker homology type", "%id. target Large yellow croaker gene identical to query gene", 
          "%id. query gene identical to target Large yellow croaker gene", 
          "Large yellow croaker Gene-order conservation score", 
          "Large yellow croaker Whole-genome alignment coverage", 
          "Large yellow croaker orthology confidence [0 low, 1 high]", 
          "Leishan spiny toad gene stable ID", "Leishan spiny toad gene name", 
          "Leishan spiny toad protein or transcript stable ID", 
          "Leishan spiny toad chromosome/scaffold name", "Leishan spiny toad chromosome/scaffold start (bp)", 
          "Leishan spiny toad chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Leishan spiny toad", "Leishan spiny toad homology type", 
          "%id. target Leishan spiny toad gene identical to query gene", 
          "%id. query gene identical to target Leishan spiny toad gene", 
          "Leishan spiny toad Gene-order conservation score", "Leishan spiny toad Whole-genome alignment coverage", 
          "Leishan spiny toad orthology confidence [0 low, 1 high]", 
          "Leopard gene stable ID", "Leopard gene name", "Leopard protein or transcript stable ID", 
          "Leopard chromosome/scaffold name", "Leopard chromosome/scaffold start (bp)", 
          "Leopard chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Leopard", "Leopard homology type", 
          "%id. target Leopard gene identical to query gene", "%id. query gene identical to target Leopard gene", 
          "Leopard Gene-order conservation score", "Leopard Whole-genome alignment coverage", 
          "Leopard orthology confidence [0 low, 1 high]", "Lesser Egyptian jerboa gene stable ID", 
          "Lesser Egyptian jerboa gene name", "Lesser Egyptian jerboa protein or transcript stable ID", 
          "Lesser Egyptian jerboa chromosome/scaffold name", "Lesser Egyptian jerboa chromosome/scaffold start (bp)", 
          "Lesser Egyptian jerboa chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Lesser Egyptian jerboa", 
          "Lesser Egyptian jerboa homology type", "%id. target Lesser Egyptian jerboa gene identical to query gene", 
          "%id. query gene identical to target Lesser Egyptian jerboa gene", 
          "Lesser Egyptian jerboa Gene-order conservation score", 
          "Lesser Egyptian jerboa Whole-genome alignment coverage", 
          "Lesser Egyptian jerboa orthology confidence [0 low, 1 high]", 
          "Lesser hedgehog tenrec gene stable ID", "Lesser hedgehog tenrec gene name", 
          "Lesser hedgehog tenrec protein or transcript stable ID", 
          "Lesser hedgehog tenrec chromosome/scaffold name", "Lesser hedgehog tenrec chromosome/scaffold start (bp)", 
          "Lesser hedgehog tenrec chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Lesser hedgehog tenrec", 
          "Lesser hedgehog tenrec homology type", "%id. target Lesser hedgehog tenrec gene identical to query gene", 
          "%id. query gene identical to target Lesser hedgehog tenrec gene", 
          "Lesser hedgehog tenrec Gene-order conservation score", 
          "Lesser hedgehog tenrec Whole-genome alignment coverage", 
          "Lesser hedgehog tenrec orthology confidence [0 low, 1 high]", 
          "Lion gene stable ID", "Lion gene name", "Lion protein or transcript stable ID", 
          "Lion chromosome/scaffold name", "Lion chromosome/scaffold start (bp)", 
          "Lion chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Lion", "Lion homology type", 
          "%id. target Lion gene identical to query gene", "%id. query gene identical to target Lion gene", 
          "Lion Gene-order conservation score", "Lion Whole-genome alignment coverage", 
          "Lion orthology confidence [0 low, 1 high]", "Long-tailed chinchilla gene stable ID", 
          "Long-tailed chinchilla gene name", "Long-tailed chinchilla protein or transcript stable ID", 
          "Long-tailed chinchilla chromosome/scaffold name", "Long-tailed chinchilla chromosome/scaffold start (bp)", 
          "Long-tailed chinchilla chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Long-tailed chinchilla", 
          "Long-tailed chinchilla homology type", "%id. target Long-tailed chinchilla gene identical to query gene", 
          "%id. query gene identical to target Long-tailed chinchilla gene", 
          "Long-tailed chinchilla Gene-order conservation score", 
          "Long-tailed chinchilla Whole-genome alignment coverage", 
          "Long-tailed chinchilla orthology confidence [0 low, 1 high]", 
          "Lumpfish gene stable ID", "Lumpfish gene name", "Lumpfish protein or transcript stable ID", 
          "Lumpfish chromosome/scaffold name", "Lumpfish chromosome/scaffold start (bp)", 
          "Lumpfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Lumpfish", "Lumpfish homology type", 
          "%id. target Lumpfish gene identical to query gene", 
          "%id. query gene identical to target Lumpfish gene", 
          "Lumpfish Gene-order conservation score", "Lumpfish Whole-genome alignment coverage", 
          "Lumpfish orthology confidence [0 low, 1 high]", "Lyretail cichlid gene stable ID", 
          "Lyretail cichlid gene name", "Lyretail cichlid protein or transcript stable ID", 
          "Lyretail cichlid chromosome/scaffold name", "Lyretail cichlid chromosome/scaffold start (bp)", 
          "Lyretail cichlid chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Lyretail cichlid", "Lyretail cichlid homology type", 
          "%id. target Lyretail cichlid gene identical to query gene", 
          "%id. query gene identical to target Lyretail cichlid gene", 
          "Lyretail cichlid Gene-order conservation score", "Lyretail cichlid Whole-genome alignment coverage", 
          "Lyretail cichlid orthology confidence [0 low, 1 high]", 
          "Ma's night monkey gene stable ID", "Ma's night monkey gene name", 
          "Ma's night monkey protein or transcript stable ID", 
          "Ma's night monkey chromosome/scaffold name", "Ma's night monkey chromosome/scaffold start (bp)", 
          "Ma's night monkey chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Ma's night monkey", "Ma's night monkey homology type", 
          "%id. target Ma's night monkey gene identical to query gene", 
          "%id. query gene identical to target Ma's night monkey gene", 
          "Ma's night monkey Gene-order conservation score", "Ma's night monkey Whole-genome alignment coverage", 
          "Ma's night monkey orthology confidence [0 low, 1 high]", 
          "Macaque gene stable ID", "Macaque gene name", "Macaque protein or transcript stable ID", 
          "Macaque chromosome/scaffold name", "Macaque chromosome/scaffold start (bp)", 
          "Macaque chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Macaque", "Macaque homology type", 
          "%id. target Macaque gene identical to query gene", "%id. query gene identical to target Macaque gene", 
          "Macaque Gene-order conservation score", "Macaque Whole-genome alignment coverage", 
          "Macaque orthology confidence [0 low, 1 high]", "Mainland tiger snake gene stable ID", 
          "Mainland tiger snake gene name", "Mainland tiger snake protein or transcript stable ID", 
          "Mainland tiger snake chromosome/scaffold name", "Mainland tiger snake chromosome/scaffold start (bp)", 
          "Mainland tiger snake chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Mainland tiger snake", 
          "Mainland tiger snake homology type", "%id. target Mainland tiger snake gene identical to query gene", 
          "%id. query gene identical to target Mainland tiger snake gene", 
          "Mainland tiger snake Gene-order conservation score", 
          "Mainland tiger snake Whole-genome alignment coverage", 
          "Mainland tiger snake orthology confidence [0 low, 1 high]", 
          "Makobe Island cichlid gene stable ID", "Makobe Island cichlid gene name", 
          "Makobe Island cichlid protein or transcript stable ID", 
          "Makobe Island cichlid chromosome/scaffold name", "Makobe Island cichlid chromosome/scaffold start (bp)", 
          "Makobe Island cichlid chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Makobe Island cichlid", 
          "Makobe Island cichlid homology type", "%id. target Makobe Island cichlid gene identical to query gene", 
          "%id. query gene identical to target Makobe Island cichlid gene", 
          "Makobe Island cichlid Gene-order conservation score", 
          "Makobe Island cichlid Whole-genome alignment coverage", 
          "Makobe Island cichlid orthology confidence [0 low, 1 high]", 
          "Mangrove rivulus gene stable ID", "Mangrove rivulus gene name", 
          "Mangrove rivulus protein or transcript stable ID", "Mangrove rivulus chromosome/scaffold name", 
          "Mangrove rivulus chromosome/scaffold start (bp)", "Mangrove rivulus chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Mangrove rivulus", 
          "Mangrove rivulus homology type", "%id. target Mangrove rivulus gene identical to query gene", 
          "%id. query gene identical to target Mangrove rivulus gene", 
          "Mangrove rivulus Gene-order conservation score", "Mangrove rivulus Whole-genome alignment coverage", 
          "Mangrove rivulus orthology confidence [0 low, 1 high]", 
          "Medium ground-finch gene stable ID", "Medium ground-finch gene name", 
          "Medium ground-finch protein or transcript stable ID", 
          "Medium ground-finch chromosome/scaffold name", "Medium ground-finch chromosome/scaffold start (bp)", 
          "Medium ground-finch chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Medium ground-finch", "Medium ground-finch homology type", 
          "%id. target Medium ground-finch gene identical to query gene", 
          "%id. query gene identical to target Medium ground-finch gene", 
          "Medium ground-finch Gene-order conservation score", 
          "Medium ground-finch Whole-genome alignment coverage", 
          "Medium ground-finch orthology confidence [0 low, 1 high]", 
          "Megabat gene stable ID", "Megabat gene name", "Megabat protein or transcript stable ID", 
          "Megabat chromosome/scaffold name", "Megabat chromosome/scaffold start (bp)", 
          "Megabat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Megabat", "Megabat homology type", 
          "%id. target Megabat gene identical to query gene", "%id. query gene identical to target Megabat gene", 
          "Megabat Gene-order conservation score", "Megabat Whole-genome alignment coverage", 
          "Megabat orthology confidence [0 low, 1 high]", "Mexican tetra gene stable ID", 
          "Mexican tetra gene name", "Mexican tetra protein or transcript stable ID", 
          "Mexican tetra chromosome/scaffold name", "Mexican tetra chromosome/scaffold start (bp)", 
          "Mexican tetra chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Mexican tetra", "Mexican tetra homology type", 
          "%id. target Mexican tetra gene identical to query gene", 
          "%id. query gene identical to target Mexican tetra gene", 
          "Mexican tetra Gene-order conservation score", "Mexican tetra Whole-genome alignment coverage", 
          "Mexican tetra orthology confidence [0 low, 1 high]", 
          "Microbat gene stable ID", "Microbat gene name", "Microbat protein or transcript stable ID", 
          "Microbat chromosome/scaffold name", "Microbat chromosome/scaffold start (bp)", 
          "Microbat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Microbat", "Microbat homology type", 
          "%id. target Microbat gene identical to query gene", 
          "%id. query gene identical to target Microbat gene", 
          "Microbat Gene-order conservation score", "Microbat Whole-genome alignment coverage", 
          "Microbat orthology confidence [0 low, 1 high]", "Midas cichlid gene stable ID", 
          "Midas cichlid gene name", "Midas cichlid protein or transcript stable ID", 
          "Midas cichlid chromosome/scaffold name", "Midas cichlid chromosome/scaffold start (bp)", 
          "Midas cichlid chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Midas cichlid", "Midas cichlid homology type", 
          "%id. target Midas cichlid gene identical to query gene", 
          "%id. query gene identical to target Midas cichlid gene", 
          "Midas cichlid Gene-order conservation score", "Midas cichlid Whole-genome alignment coverage", 
          "Midas cichlid orthology confidence [0 low, 1 high]", 
          "Mouse gene stable ID", "Mouse gene name", "Mouse protein or transcript stable ID", 
          "Mouse chromosome/scaffold name", "Mouse chromosome/scaffold start (bp)", 
          "Mouse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Mouse", "Mouse homology type", 
          "%id. target Mouse gene identical to query gene", "%id. query gene identical to target Mouse gene", 
          "Mouse Gene-order conservation score", "Mouse Whole-genome alignment coverage", 
          "Mouse orthology confidence [0 low, 1 high]", "Mouse Lemur gene stable ID", 
          "Mouse Lemur gene name", "Mouse Lemur protein or transcript stable ID", 
          "Mouse Lemur chromosome/scaffold name", "Mouse Lemur chromosome/scaffold start (bp)", 
          "Mouse Lemur chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Mouse Lemur", "Mouse Lemur homology type", 
          "%id. target Mouse Lemur gene identical to query gene", 
          "%id. query gene identical to target Mouse Lemur gene", 
          "Mouse Lemur Gene-order conservation score", "Mouse Lemur Whole-genome alignment coverage", 
          "Mouse Lemur orthology confidence [0 low, 1 high]", "Mummichog gene stable ID", 
          "Mummichog gene name", "Mummichog protein or transcript stable ID", 
          "Mummichog chromosome/scaffold name", "Mummichog chromosome/scaffold start (bp)", 
          "Mummichog chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Mummichog", "Mummichog homology type", 
          "%id. target Mummichog gene identical to query gene", 
          "%id. query gene identical to target Mummichog gene", 
          "Mummichog Gene-order conservation score", "Mummichog Whole-genome alignment coverage", 
          "Mummichog orthology confidence [0 low, 1 high]", "Naked mole-rat female gene stable ID", 
          "Naked mole-rat female gene name", "Naked mole-rat female protein or transcript stable ID", 
          "Naked mole-rat female chromosome/scaffold name", "Naked mole-rat female chromosome/scaffold start (bp)", 
          "Naked mole-rat female chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Naked mole-rat female", 
          "Naked mole-rat female homology type", "%id. target Naked mole-rat female gene identical to query gene", 
          "%id. query gene identical to target Naked mole-rat female gene", 
          "Naked mole-rat female Gene-order conservation score", 
          "Naked mole-rat female Whole-genome alignment coverage", 
          "Naked mole-rat female orthology confidence [0 low, 1 high]", 
          "Narwhal gene stable ID", "Narwhal gene name", "Narwhal protein or transcript stable ID", 
          "Narwhal chromosome/scaffold name", "Narwhal chromosome/scaffold start (bp)", 
          "Narwhal chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Narwhal", "Narwhal homology type", 
          "%id. target Narwhal gene identical to query gene", "%id. query gene identical to target Narwhal gene", 
          "Narwhal Gene-order conservation score", "Narwhal Whole-genome alignment coverage", 
          "Narwhal orthology confidence [0 low, 1 high]", "Nile tilapia gene stable ID", 
          "Nile tilapia gene name", "Nile tilapia protein or transcript stable ID", 
          "Nile tilapia chromosome/scaffold name", "Nile tilapia chromosome/scaffold start (bp)", 
          "Nile tilapia chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Nile tilapia", "Nile tilapia homology type", 
          "%id. target Nile tilapia gene identical to query gene", 
          "%id. query gene identical to target Nile tilapia gene", 
          "Nile tilapia Gene-order conservation score", "Nile tilapia Whole-genome alignment coverage", 
          "Nile tilapia orthology confidence [0 low, 1 high]", 
          "Northern American deer mouse gene stable ID", "Northern American deer mouse gene name", 
          "Northern American deer mouse protein or transcript stable ID", 
          "Northern American deer mouse chromosome/scaffold name", 
          "Northern American deer mouse chromosome/scaffold start (bp)", 
          "Northern American deer mouse chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Northern American deer mouse", 
          "Northern American deer mouse homology type", "%id. target Northern American deer mouse gene identical to query gene", 
          "%id. query gene identical to target Northern American deer mouse gene", 
          "Northern American deer mouse Gene-order conservation score", 
          "Northern American deer mouse Whole-genome alignment coverage", 
          "Northern American deer mouse orthology confidence [0 low, 1 high]", 
          "Northern pike gene stable ID", "Northern pike gene name", 
          "Northern pike protein or transcript stable ID", "Northern pike chromosome/scaffold name", 
          "Northern pike chromosome/scaffold start (bp)", "Northern pike chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Northern pike", 
          "Northern pike homology type", "%id. target Northern pike gene identical to query gene", 
          "%id. query gene identical to target Northern pike gene", 
          "Northern pike Gene-order conservation score", "Northern pike Whole-genome alignment coverage", 
          "Northern pike orthology confidence [0 low, 1 high]", 
          "Olive baboon gene stable ID", "Olive baboon gene name", 
          "Olive baboon protein or transcript stable ID", "Olive baboon chromosome/scaffold name", 
          "Olive baboon chromosome/scaffold start (bp)", "Olive baboon chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Olive baboon", 
          "Olive baboon homology type", "%id. target Olive baboon gene identical to query gene", 
          "%id. query gene identical to target Olive baboon gene", 
          "Olive baboon Gene-order conservation score", "Olive baboon Whole-genome alignment coverage", 
          "Olive baboon orthology confidence [0 low, 1 high]", 
          "Opossum gene stable ID", "Opossum gene name", "Opossum protein or transcript stable ID", 
          "Opossum chromosome/scaffold name", "Opossum chromosome/scaffold start (bp)", 
          "Opossum chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Opossum", "Opossum homology type", 
          "%id. target Opossum gene identical to query gene", "%id. query gene identical to target Opossum gene", 
          "Opossum Gene-order conservation score", "Opossum Whole-genome alignment coverage", 
          "Opossum orthology confidence [0 low, 1 high]", "Orange clownfish gene stable ID", 
          "Orange clownfish gene name", "Orange clownfish protein or transcript stable ID", 
          "Orange clownfish chromosome/scaffold name", "Orange clownfish chromosome/scaffold start (bp)", 
          "Orange clownfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Orange clownfish", "Orange clownfish homology type", 
          "%id. target Orange clownfish gene identical to query gene", 
          "%id. query gene identical to target Orange clownfish gene", 
          "Orange clownfish Gene-order conservation score", "Orange clownfish Whole-genome alignment coverage", 
          "Orange clownfish orthology confidence [0 low, 1 high]", 
          "Painted turtle gene stable ID", "Painted turtle gene name", 
          "Painted turtle protein or transcript stable ID", "Painted turtle chromosome/scaffold name", 
          "Painted turtle chromosome/scaffold start (bp)", "Painted turtle chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Painted turtle", 
          "Painted turtle homology type", "%id. target Painted turtle gene identical to query gene", 
          "%id. query gene identical to target Painted turtle gene", 
          "Painted turtle Gene-order conservation score", "Painted turtle Whole-genome alignment coverage", 
          "Painted turtle orthology confidence [0 low, 1 high]", 
          "Paramormyrops kingsleyae gene stable ID", "Paramormyrops kingsleyae gene name", 
          "Paramormyrops kingsleyae protein or transcript stable ID", 
          "Paramormyrops kingsleyae chromosome/scaffold name", 
          "Paramormyrops kingsleyae chromosome/scaffold start (bp)", 
          "Paramormyrops kingsleyae chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Paramormyrops kingsleyae", 
          "Paramormyrops kingsleyae homology type", "%id. target Paramormyrops kingsleyae gene identical to query gene", 
          "%id. query gene identical to target Paramormyrops kingsleyae gene", 
          "Paramormyrops kingsleyae Gene-order conservation score", 
          "Paramormyrops kingsleyae Whole-genome alignment coverage", 
          "Paramormyrops kingsleyae orthology confidence [0 low, 1 high]", 
          "Pig gene stable ID", "Pig gene name", "Pig protein or transcript stable ID", 
          "Pig chromosome/scaffold name", "Pig chromosome/scaffold start (bp)", 
          "Pig chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Pig", "Pig homology type", 
          "%id. target Pig gene identical to query gene", "%id. query gene identical to target Pig gene", 
          "Pig Gene-order conservation score", "Pig Whole-genome alignment coverage", 
          "Pig orthology confidence [0 low, 1 high]", "Pig-tailed macaque gene stable ID", 
          "Pig-tailed macaque gene name", "Pig-tailed macaque protein or transcript stable ID", 
          "Pig-tailed macaque chromosome/scaffold name", "Pig-tailed macaque chromosome/scaffold start (bp)", 
          "Pig-tailed macaque chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Pig-tailed macaque", "Pig-tailed macaque homology type", 
          "%id. target Pig-tailed macaque gene identical to query gene", 
          "%id. query gene identical to target Pig-tailed macaque gene", 
          "Pig-tailed macaque Gene-order conservation score", "Pig-tailed macaque Whole-genome alignment coverage", 
          "Pig-tailed macaque orthology confidence [0 low, 1 high]", 
          "Pika gene stable ID", "Pika gene name", "Pika protein or transcript stable ID", 
          "Pika chromosome/scaffold name", "Pika chromosome/scaffold start (bp)", 
          "Pika chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Pika", "Pika homology type", 
          "%id. target Pika gene identical to query gene", "%id. query gene identical to target Pika gene", 
          "Pika Gene-order conservation score", "Pika Whole-genome alignment coverage", 
          "Pika orthology confidence [0 low, 1 high]", "Pike-perch gene stable ID", 
          "Pike-perch gene name", "Pike-perch protein or transcript stable ID", 
          "Pike-perch chromosome/scaffold name", "Pike-perch chromosome/scaffold start (bp)", 
          "Pike-perch chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Pike-perch", "Pike-perch homology type", 
          "%id. target Pike-perch gene identical to query gene", 
          "%id. query gene identical to target Pike-perch gene", 
          "Pike-perch Gene-order conservation score", "Pike-perch Whole-genome alignment coverage", 
          "Pike-perch orthology confidence [0 low, 1 high]", "Pinecone soldierfish gene stable ID", 
          "Pinecone soldierfish gene name", "Pinecone soldierfish protein or transcript stable ID", 
          "Pinecone soldierfish chromosome/scaffold name", "Pinecone soldierfish chromosome/scaffold start (bp)", 
          "Pinecone soldierfish chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Pinecone soldierfish", 
          "Pinecone soldierfish homology type", "%id. target Pinecone soldierfish gene identical to query gene", 
          "%id. query gene identical to target Pinecone soldierfish gene", 
          "Pinecone soldierfish Gene-order conservation score", 
          "Pinecone soldierfish Whole-genome alignment coverage", 
          "Pinecone soldierfish orthology confidence [0 low, 1 high]", 
          "Pink-footed goose gene stable ID", "Pink-footed goose gene name", 
          "Pink-footed goose protein or transcript stable ID", 
          "Pink-footed goose chromosome/scaffold name", "Pink-footed goose chromosome/scaffold start (bp)", 
          "Pink-footed goose chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Pink-footed goose", "Pink-footed goose homology type", 
          "%id. target Pink-footed goose gene identical to query gene", 
          "%id. query gene identical to target Pink-footed goose gene", 
          "Pink-footed goose Gene-order conservation score", "Pink-footed goose Whole-genome alignment coverage", 
          "Pink-footed goose orthology confidence [0 low, 1 high]", 
          "Platyfish gene stable ID", "Platyfish gene name", "Platyfish protein or transcript stable ID", 
          "Platyfish chromosome/scaffold name", "Platyfish chromosome/scaffold start (bp)", 
          "Platyfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Platyfish", "Platyfish homology type", 
          "%id. target Platyfish gene identical to query gene", 
          "%id. query gene identical to target Platyfish gene", 
          "Platyfish Gene-order conservation score", "Platyfish Whole-genome alignment coverage", 
          "Platyfish orthology confidence [0 low, 1 high]", "Platypus gene stable ID", 
          "Platypus gene name", "Platypus protein or transcript stable ID", 
          "Platypus chromosome/scaffold name", "Platypus chromosome/scaffold start (bp)", 
          "Platypus chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Platypus", "Platypus homology type", 
          "%id. target Platypus gene identical to query gene", 
          "%id. query gene identical to target Platypus gene", 
          "Platypus Gene-order conservation score", "Platypus Whole-genome alignment coverage", 
          "Platypus orthology confidence [0 low, 1 high]", "Polar bear gene stable ID", 
          "Polar bear gene name", "Polar bear protein or transcript stable ID", 
          "Polar bear chromosome/scaffold name", "Polar bear chromosome/scaffold start (bp)", 
          "Polar bear chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Polar bear", "Polar bear homology type", 
          "%id. target Polar bear gene identical to query gene", 
          "%id. query gene identical to target Polar bear gene", 
          "Polar bear Gene-order conservation score", "Polar bear Whole-genome alignment coverage", 
          "Polar bear orthology confidence [0 low, 1 high]", "Prairie vole gene stable ID", 
          "Prairie vole gene name", "Prairie vole protein or transcript stable ID", 
          "Prairie vole chromosome/scaffold name", "Prairie vole chromosome/scaffold start (bp)", 
          "Prairie vole chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Prairie vole", "Prairie vole homology type", 
          "%id. target Prairie vole gene identical to query gene", 
          "%id. query gene identical to target Prairie vole gene", 
          "Prairie vole Gene-order conservation score", "Prairie vole Whole-genome alignment coverage", 
          "Prairie vole orthology confidence [0 low, 1 high]", 
          "Rabbit gene stable ID", "Rabbit gene name", "Rabbit protein or transcript stable ID", 
          "Rabbit chromosome/scaffold name", "Rabbit chromosome/scaffold start (bp)", 
          "Rabbit chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Rabbit", "Rabbit homology type", 
          "%id. target Rabbit gene identical to query gene", "%id. query gene identical to target Rabbit gene", 
          "Rabbit Gene-order conservation score", "Rabbit Whole-genome alignment coverage", 
          "Rabbit orthology confidence [0 low, 1 high]", "Rainbow trout gene stable ID", 
          "Rainbow trout gene name", "Rainbow trout protein or transcript stable ID", 
          "Rainbow trout chromosome/scaffold name", "Rainbow trout chromosome/scaffold start (bp)", 
          "Rainbow trout chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Rainbow trout", "Rainbow trout homology type", 
          "%id. target Rainbow trout gene identical to query gene", 
          "%id. query gene identical to target Rainbow trout gene", 
          "Rainbow trout Gene-order conservation score", "Rainbow trout Whole-genome alignment coverage", 
          "Rainbow trout orthology confidence [0 low, 1 high]", 
          "Rat gene stable ID", "Rat gene name", "Rat protein or transcript stable ID", 
          "Rat chromosome/scaffold name", "Rat chromosome/scaffold start (bp)", 
          "Rat chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Rat", "Rat homology type", 
          "%id. target Rat gene identical to query gene", "%id. query gene identical to target Rat gene", 
          "Rat Gene-order conservation score", "Rat Whole-genome alignment coverage", 
          "Rat orthology confidence [0 low, 1 high]", "Red fox gene stable ID", 
          "Red fox gene name", "Red fox protein or transcript stable ID", 
          "Red fox chromosome/scaffold name", "Red fox chromosome/scaffold start (bp)", 
          "Red fox chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Red fox", "Red fox homology type", 
          "%id. target Red fox gene identical to query gene", "%id. query gene identical to target Red fox gene", 
          "Red fox Gene-order conservation score", "Red fox Whole-genome alignment coverage", 
          "Red fox orthology confidence [0 low, 1 high]", "Red-bellied piranha gene stable ID", 
          "Red-bellied piranha gene name", "Red-bellied piranha protein or transcript stable ID", 
          "Red-bellied piranha chromosome/scaffold name", "Red-bellied piranha chromosome/scaffold start (bp)", 
          "Red-bellied piranha chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Red-bellied piranha", "Red-bellied piranha homology type", 
          "%id. target Red-bellied piranha gene identical to query gene", 
          "%id. query gene identical to target Red-bellied piranha gene", 
          "Red-bellied piranha Gene-order conservation score", 
          "Red-bellied piranha Whole-genome alignment coverage", 
          "Red-bellied piranha orthology confidence [0 low, 1 high]", 
          "Reedfish gene stable ID", "Reedfish gene name", "Reedfish protein or transcript stable ID", 
          "Reedfish chromosome/scaffold name", "Reedfish chromosome/scaffold start (bp)", 
          "Reedfish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Reedfish", "Reedfish homology type", 
          "%id. target Reedfish gene identical to query gene", 
          "%id. query gene identical to target Reedfish gene", 
          "Reedfish Gene-order conservation score", "Reedfish Whole-genome alignment coverage", 
          "Reedfish orthology confidence [0 low, 1 high]", "Ryukyu mouse gene stable ID", 
          "Ryukyu mouse gene name", "Ryukyu mouse protein or transcript stable ID", 
          "Ryukyu mouse chromosome/scaffold name", "Ryukyu mouse chromosome/scaffold start (bp)", 
          "Ryukyu mouse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Ryukyu mouse", "Ryukyu mouse homology type", 
          "%id. target Ryukyu mouse gene identical to query gene", 
          "%id. query gene identical to target Ryukyu mouse gene", 
          "Ryukyu mouse Gene-order conservation score", "Ryukyu mouse Whole-genome alignment coverage", 
          "Ryukyu mouse orthology confidence [0 low, 1 high]", 
          "Saccharomyces cerevisiae gene stable ID", "Saccharomyces cerevisiae gene name", 
          "Saccharomyces cerevisiae protein or transcript stable ID", 
          "Saccharomyces cerevisiae chromosome/scaffold name", 
          "Saccharomyces cerevisiae chromosome/scaffold start (bp)", 
          "Saccharomyces cerevisiae chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Saccharomyces cerevisiae", 
          "Saccharomyces cerevisiae homology type", "%id. target Saccharomyces cerevisiae gene identical to query gene", 
          "%id. query gene identical to target Saccharomyces cerevisiae gene", 
          "Saccharomyces cerevisiae orthology confidence [0 low, 1 high]", 
          "Sailfin molly gene stable ID", "Sailfin molly gene name", 
          "Sailfin molly protein or transcript stable ID", "Sailfin molly chromosome/scaffold name", 
          "Sailfin molly chromosome/scaffold start (bp)", "Sailfin molly chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Sailfin molly", 
          "Sailfin molly homology type", "%id. target Sailfin molly gene identical to query gene", 
          "%id. query gene identical to target Sailfin molly gene", 
          "Sailfin molly Gene-order conservation score", "Sailfin molly Whole-genome alignment coverage", 
          "Sailfin molly orthology confidence [0 low, 1 high]", 
          "Sheep gene stable ID", "Sheep gene name", "Sheep protein or transcript stable ID", 
          "Sheep chromosome/scaffold name", "Sheep chromosome/scaffold start (bp)", 
          "Sheep chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Sheep", "Sheep homology type", 
          "%id. target Sheep gene identical to query gene", "%id. query gene identical to target Sheep gene", 
          "Sheep Gene-order conservation score", "Sheep Whole-genome alignment coverage", 
          "Sheep orthology confidence [0 low, 1 high]", "Sheepshead minnow gene stable ID", 
          "Sheepshead minnow gene name", "Sheepshead minnow protein or transcript stable ID", 
          "Sheepshead minnow chromosome/scaffold name", "Sheepshead minnow chromosome/scaffold start (bp)", 
          "Sheepshead minnow chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Sheepshead minnow", "Sheepshead minnow homology type", 
          "%id. target Sheepshead minnow gene identical to query gene", 
          "%id. query gene identical to target Sheepshead minnow gene", 
          "Sheepshead minnow Gene-order conservation score", "Sheepshead minnow Whole-genome alignment coverage", 
          "Sheepshead minnow orthology confidence [0 low, 1 high]", 
          "Shrew gene stable ID", "Shrew gene name", "Shrew protein or transcript stable ID", 
          "Shrew chromosome/scaffold name", "Shrew chromosome/scaffold start (bp)", 
          "Shrew chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Shrew", "Shrew homology type", 
          "%id. target Shrew gene identical to query gene", "%id. query gene identical to target Shrew gene", 
          "Shrew Gene-order conservation score", "Shrew Whole-genome alignment coverage", 
          "Shrew orthology confidence [0 low, 1 high]", "Shrew mouse gene stable ID", 
          "Shrew mouse gene name", "Shrew mouse protein or transcript stable ID", 
          "Shrew mouse chromosome/scaffold name", "Shrew mouse chromosome/scaffold start (bp)", 
          "Shrew mouse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Shrew mouse", "Shrew mouse homology type", 
          "%id. target Shrew mouse gene identical to query gene", 
          "%id. query gene identical to target Shrew mouse gene", 
          "Shrew mouse Gene-order conservation score", "Shrew mouse Whole-genome alignment coverage", 
          "Shrew mouse orthology confidence [0 low, 1 high]", "Siamese fighting fish gene stable ID", 
          "Siamese fighting fish gene name", "Siamese fighting fish protein or transcript stable ID", 
          "Siamese fighting fish chromosome/scaffold name", "Siamese fighting fish chromosome/scaffold start (bp)", 
          "Siamese fighting fish chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Siamese fighting fish", 
          "Siamese fighting fish homology type", "%id. target Siamese fighting fish gene identical to query gene", 
          "%id. query gene identical to target Siamese fighting fish gene", 
          "Siamese fighting fish Gene-order conservation score", 
          "Siamese fighting fish Whole-genome alignment coverage", 
          "Siamese fighting fish orthology confidence [0 low, 1 high]", 
          "Siberian musk deer gene stable ID", "Siberian musk deer gene name", 
          "Siberian musk deer protein or transcript stable ID", 
          "Siberian musk deer chromosome/scaffold name", "Siberian musk deer chromosome/scaffold start (bp)", 
          "Siberian musk deer chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Siberian musk deer", "Siberian musk deer homology type", 
          "%id. target Siberian musk deer gene identical to query gene", 
          "%id. query gene identical to target Siberian musk deer gene", 
          "Siberian musk deer Gene-order conservation score", "Siberian musk deer Whole-genome alignment coverage", 
          "Siberian musk deer orthology confidence [0 low, 1 high]", 
          "Sloth gene stable ID", "Sloth gene name", "Sloth protein or transcript stable ID", 
          "Sloth chromosome/scaffold name", "Sloth chromosome/scaffold start (bp)", 
          "Sloth chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Sloth", "Sloth homology type", 
          "%id. target Sloth gene identical to query gene", "%id. query gene identical to target Sloth gene", 
          "Sloth Gene-order conservation score", "Sloth Whole-genome alignment coverage", 
          "Sloth orthology confidence [0 low, 1 high]", "Sooty mangabey gene stable ID", 
          "Sooty mangabey gene name", "Sooty mangabey protein or transcript stable ID", 
          "Sooty mangabey chromosome/scaffold name", "Sooty mangabey chromosome/scaffold start (bp)", 
          "Sooty mangabey chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Sooty mangabey", "Sooty mangabey homology type", 
          "%id. target Sooty mangabey gene identical to query gene", 
          "%id. query gene identical to target Sooty mangabey gene", 
          "Sooty mangabey Gene-order conservation score", "Sooty mangabey Whole-genome alignment coverage", 
          "Sooty mangabey orthology confidence [0 low, 1 high]", 
          "Sperm whale gene stable ID", "Sperm whale gene name", 
          "Sperm whale protein or transcript stable ID", "Sperm whale chromosome/scaffold name", 
          "Sperm whale chromosome/scaffold start (bp)", "Sperm whale chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Sperm whale", 
          "Sperm whale homology type", "%id. target Sperm whale gene identical to query gene", 
          "%id. query gene identical to target Sperm whale gene", 
          "Sperm whale Gene-order conservation score", "Sperm whale Whole-genome alignment coverage", 
          "Sperm whale orthology confidence [0 low, 1 high]", "Spiny chromis gene stable ID", 
          "Spiny chromis gene name", "Spiny chromis protein or transcript stable ID", 
          "Spiny chromis chromosome/scaffold name", "Spiny chromis chromosome/scaffold start (bp)", 
          "Spiny chromis chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Spiny chromis", "Spiny chromis homology type", 
          "%id. target Spiny chromis gene identical to query gene", 
          "%id. query gene identical to target Spiny chromis gene", 
          "Spiny chromis Gene-order conservation score", "Spiny chromis Whole-genome alignment coverage", 
          "Spiny chromis orthology confidence [0 low, 1 high]", 
          "Spotted gar gene stable ID", "Spotted gar gene name", 
          "Spotted gar protein or transcript stable ID", "Spotted gar chromosome/scaffold name", 
          "Spotted gar chromosome/scaffold start (bp)", "Spotted gar chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Spotted gar", 
          "Spotted gar homology type", "%id. target Spotted gar gene identical to query gene", 
          "%id. query gene identical to target Spotted gar gene", 
          "Spotted gar Gene-order conservation score", "Spotted gar Whole-genome alignment coverage", 
          "Spotted gar orthology confidence [0 low, 1 high]", "Squirrel gene stable ID", 
          "Squirrel gene name", "Squirrel protein or transcript stable ID", 
          "Squirrel chromosome/scaffold name", "Squirrel chromosome/scaffold start (bp)", 
          "Squirrel chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Squirrel", "Squirrel homology type", 
          "%id. target Squirrel gene identical to query gene", 
          "%id. query gene identical to target Squirrel gene", 
          "Squirrel Gene-order conservation score", "Squirrel Whole-genome alignment coverage", 
          "Squirrel orthology confidence [0 low, 1 high]", "Steppe mouse gene stable ID", 
          "Steppe mouse gene name", "Steppe mouse protein or transcript stable ID", 
          "Steppe mouse chromosome/scaffold name", "Steppe mouse chromosome/scaffold start (bp)", 
          "Steppe mouse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Steppe mouse", "Steppe mouse homology type", 
          "%id. target Steppe mouse gene identical to query gene", 
          "%id. query gene identical to target Steppe mouse gene", 
          "Steppe mouse Gene-order conservation score", "Steppe mouse Whole-genome alignment coverage", 
          "Steppe mouse orthology confidence [0 low, 1 high]", 
          "Stickleback gene stable ID", "Stickleback gene name", 
          "Stickleback protein or transcript stable ID", "Stickleback chromosome/scaffold name", 
          "Stickleback chromosome/scaffold start (bp)", "Stickleback chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Stickleback", 
          "Stickleback homology type", "%id. target Stickleback gene identical to query gene", 
          "%id. query gene identical to target Stickleback gene", 
          "Stickleback Gene-order conservation score", "Stickleback Whole-genome alignment coverage", 
          "Stickleback orthology confidence [0 low, 1 high]", "Sumatran orangutan gene stable ID", 
          "Sumatran orangutan gene name", "Sumatran orangutan protein or transcript stable ID", 
          "Sumatran orangutan chromosome/scaffold name", "Sumatran orangutan chromosome/scaffold start (bp)", 
          "Sumatran orangutan chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Sumatran orangutan", "Sumatran orangutan homology type", 
          "%id. target Sumatran orangutan gene identical to query gene", 
          "%id. query gene identical to target Sumatran orangutan gene", 
          "Sumatran orangutan Gene-order conservation score", "Sumatran orangutan Whole-genome alignment coverage", 
          "Sumatran orangutan orthology confidence [0 low, 1 high]", 
          "Tarsier gene stable ID", "Tarsier gene name", "Tarsier protein or transcript stable ID", 
          "Tarsier chromosome/scaffold name", "Tarsier chromosome/scaffold start (bp)", 
          "Tarsier chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tarsier", "Tarsier homology type", 
          "%id. target Tarsier gene identical to query gene", "%id. query gene identical to target Tarsier gene", 
          "Tarsier Gene-order conservation score", "Tarsier Whole-genome alignment coverage", 
          "Tarsier orthology confidence [0 low, 1 high]", "Tasmanian devil gene stable ID", 
          "Tasmanian devil gene name", "Tasmanian devil protein or transcript stable ID", 
          "Tasmanian devil chromosome/scaffold name", "Tasmanian devil chromosome/scaffold start (bp)", 
          "Tasmanian devil chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tasmanian devil", "Tasmanian devil homology type", 
          "%id. target Tasmanian devil gene identical to query gene", 
          "%id. query gene identical to target Tasmanian devil gene", 
          "Tasmanian devil Gene-order conservation score", "Tasmanian devil orthology confidence [0 low, 1 high]", 
          "Tetraodon gene stable ID", "Tetraodon gene name", "Tetraodon protein or transcript stable ID", 
          "Tetraodon chromosome/scaffold name", "Tetraodon chromosome/scaffold start (bp)", 
          "Tetraodon chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tetraodon", "Tetraodon homology type", 
          "%id. target Tetraodon gene identical to query gene", 
          "%id. query gene identical to target Tetraodon gene", 
          "Tetraodon Gene-order conservation score", "Tetraodon Whole-genome alignment coverage", 
          "Tetraodon orthology confidence [0 low, 1 high]", "Three-toed box turtle gene stable ID", 
          "Three-toed box turtle gene name", "Three-toed box turtle protein or transcript stable ID", 
          "Three-toed box turtle chromosome/scaffold name", "Three-toed box turtle chromosome/scaffold start (bp)", 
          "Three-toed box turtle chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Three-toed box turtle", 
          "Three-toed box turtle homology type", "%id. target Three-toed box turtle gene identical to query gene", 
          "%id. query gene identical to target Three-toed box turtle gene", 
          "Three-toed box turtle Gene-order conservation score", 
          "Three-toed box turtle Whole-genome alignment coverage", 
          "Three-toed box turtle orthology confidence [0 low, 1 high]", 
          "Tiger gene stable ID", "Tiger gene name", "Tiger protein or transcript stable ID", 
          "Tiger chromosome/scaffold name", "Tiger chromosome/scaffold start (bp)", 
          "Tiger chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tiger", "Tiger homology type", 
          "%id. target Tiger gene identical to query gene", "%id. query gene identical to target Tiger gene", 
          "Tiger Gene-order conservation score", "Tiger Whole-genome alignment coverage", 
          "Tiger orthology confidence [0 low, 1 high]", "Tiger tail seahorse gene stable ID", 
          "Tiger tail seahorse gene name", "Tiger tail seahorse protein or transcript stable ID", 
          "Tiger tail seahorse chromosome/scaffold name", "Tiger tail seahorse chromosome/scaffold start (bp)", 
          "Tiger tail seahorse chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tiger tail seahorse", "Tiger tail seahorse homology type", 
          "%id. target Tiger tail seahorse gene identical to query gene", 
          "%id. query gene identical to target Tiger tail seahorse gene", 
          "Tiger tail seahorse Gene-order conservation score", 
          "Tiger tail seahorse Whole-genome alignment coverage", 
          "Tiger tail seahorse orthology confidence [0 low, 1 high]", 
          "Tongue sole gene stable ID", "Tongue sole gene name", 
          "Tongue sole protein or transcript stable ID", "Tongue sole chromosome/scaffold name", 
          "Tongue sole chromosome/scaffold start (bp)", "Tongue sole chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Tongue sole", 
          "Tongue sole homology type", "%id. target Tongue sole gene identical to query gene", 
          "%id. query gene identical to target Tongue sole gene", 
          "Tongue sole Gene-order conservation score", "Tongue sole Whole-genome alignment coverage", 
          "Tongue sole orthology confidence [0 low, 1 high]", "Tree Shrew gene stable ID", 
          "Tree Shrew gene name", "Tree Shrew protein or transcript stable ID", 
          "Tree Shrew chromosome/scaffold name", "Tree Shrew chromosome/scaffold start (bp)", 
          "Tree Shrew chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tree Shrew", "Tree Shrew homology type", 
          "%id. target Tree Shrew gene identical to query gene", 
          "%id. query gene identical to target Tree Shrew gene", 
          "Tree Shrew Gene-order conservation score", "Tree Shrew Whole-genome alignment coverage", 
          "Tree Shrew orthology confidence [0 low, 1 high]", "Tropical clawed frog gene stable ID", 
          "Tropical clawed frog gene name", "Tropical clawed frog protein or transcript stable ID", 
          "Tropical clawed frog chromosome/scaffold name", "Tropical clawed frog chromosome/scaffold start (bp)", 
          "Tropical clawed frog chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Tropical clawed frog", 
          "Tropical clawed frog homology type", "%id. target Tropical clawed frog gene identical to query gene", 
          "%id. query gene identical to target Tropical clawed frog gene", 
          "Tropical clawed frog Gene-order conservation score", 
          "Tropical clawed frog Whole-genome alignment coverage", 
          "Tropical clawed frog orthology confidence [0 low, 1 high]", 
          "Tuatara gene stable ID", "Tuatara gene name", "Tuatara protein or transcript stable ID", 
          "Tuatara chromosome/scaffold name", "Tuatara chromosome/scaffold start (bp)", 
          "Tuatara chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Tuatara", "Tuatara homology type", 
          "%id. target Tuatara gene identical to query gene", "%id. query gene identical to target Tuatara gene", 
          "Tuatara Gene-order conservation score", "Tuatara Whole-genome alignment coverage", 
          "Tuatara orthology confidence [0 low, 1 high]", "Turbot gene stable ID", 
          "Turbot gene name", "Turbot protein or transcript stable ID", 
          "Turbot chromosome/scaffold name", "Turbot chromosome/scaffold start (bp)", 
          "Turbot chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Turbot", "Turbot homology type", 
          "%id. target Turbot gene identical to query gene", "%id. query gene identical to target Turbot gene", 
          "Turbot Gene-order conservation score", "Turbot orthology confidence [0 low, 1 high]", 
          "Turkey gene stable ID", "Turkey gene name", "Turkey protein or transcript stable ID", 
          "Turkey chromosome/scaffold name", "Turkey chromosome/scaffold start (bp)", 
          "Turkey chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Turkey", "Turkey homology type", 
          "%id. target Turkey gene identical to query gene", "%id. query gene identical to target Turkey gene", 
          "Turkey Gene-order conservation score", "Turkey orthology confidence [0 low, 1 high]", 
          "Turquoise killifish gene stable ID", "Turquoise killifish gene name", 
          "Turquoise killifish protein or transcript stable ID", 
          "Turquoise killifish chromosome/scaffold name", "Turquoise killifish chromosome/scaffold start (bp)", 
          "Turquoise killifish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Turquoise killifish", "Turquoise killifish homology type", 
          "%id. target Turquoise killifish gene identical to query gene", 
          "%id. query gene identical to target Turquoise killifish gene", 
          "Turquoise killifish Gene-order conservation score", 
          "Turquoise killifish Whole-genome alignment coverage", 
          "Turquoise killifish orthology confidence [0 low, 1 high]", 
          "Upper Galilee mountains blind mole rat gene stable ID", 
          "Upper Galilee mountains blind mole rat gene name", "Upper Galilee mountains blind mole rat protein or transcript stable ID", 
          "Upper Galilee mountains blind mole rat chromosome/scaffold name", 
          "Upper Galilee mountains blind mole rat chromosome/scaffold start (bp)", 
          "Upper Galilee mountains blind mole rat chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Upper Galilee mountains blind mole rat", 
          "Upper Galilee mountains blind mole rat homology type", 
          "%id. target Upper Galilee mountains blind mole rat gene identical to query gene", 
          "%id. query gene identical to target Upper Galilee mountains blind mole rat gene", 
          "Upper Galilee mountains blind mole rat Gene-order conservation score", 
          "Upper Galilee mountains blind mole rat Whole-genome alignment coverage", 
          "Upper Galilee mountains blind mole rat orthology confidence [0 low, 1 high]", 
          "Vaquita gene stable ID", "Vaquita gene name", "Vaquita protein or transcript stable ID", 
          "Vaquita chromosome/scaffold name", "Vaquita chromosome/scaffold start (bp)", 
          "Vaquita chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Vaquita", "Vaquita homology type", 
          "%id. target Vaquita gene identical to query gene", "%id. query gene identical to target Vaquita gene", 
          "Vaquita Gene-order conservation score", "Vaquita Whole-genome alignment coverage", 
          "Vaquita orthology confidence [0 low, 1 high]", "Vervet-AGM gene stable ID", 
          "Vervet-AGM gene name", "Vervet-AGM protein or transcript stable ID", 
          "Vervet-AGM chromosome/scaffold name", "Vervet-AGM chromosome/scaffold start (bp)", 
          "Vervet-AGM chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Vervet-AGM", "Vervet-AGM homology type", 
          "%id. target Vervet-AGM gene identical to query gene", 
          "%id. query gene identical to target Vervet-AGM gene", 
          "Vervet-AGM Gene-order conservation score", "Vervet-AGM Whole-genome alignment coverage", 
          "Vervet-AGM orthology confidence [0 low, 1 high]", "Wallaby gene stable ID", 
          "Wallaby gene name", "Wallaby protein or transcript stable ID", 
          "Wallaby chromosome/scaffold name", "Wallaby chromosome/scaffold start (bp)", 
          "Wallaby chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Wallaby", "Wallaby homology type", 
          "%id. target Wallaby gene identical to query gene", "%id. query gene identical to target Wallaby gene", 
          "Wallaby Gene-order conservation score", "Wallaby Whole-genome alignment coverage", 
          "Wallaby orthology confidence [0 low, 1 high]", "White-tufted-ear marmoset gene stable ID", 
          "White-tufted-ear marmoset gene name", "White-tufted-ear marmoset protein or transcript stable ID", 
          "White-tufted-ear marmoset chromosome/scaffold name", 
          "White-tufted-ear marmoset chromosome/scaffold start (bp)", 
          "White-tufted-ear marmoset chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with White-tufted-ear marmoset", 
          "White-tufted-ear marmoset homology type", "%id. target White-tufted-ear marmoset gene identical to query gene", 
          "%id. query gene identical to target White-tufted-ear marmoset gene", 
          "White-tufted-ear marmoset Gene-order conservation score", 
          "White-tufted-ear marmoset Whole-genome alignment coverage", 
          "White-tufted-ear marmoset orthology confidence [0 low, 1 high]", 
          "Wild yak gene stable ID", "Wild yak gene name", "Wild yak protein or transcript stable ID", 
          "Wild yak chromosome/scaffold name", "Wild yak chromosome/scaffold start (bp)", 
          "Wild yak chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Wild yak", "Wild yak homology type", 
          "%id. target Wild yak gene identical to query gene", 
          "%id. query gene identical to target Wild yak gene", 
          "Wild yak Gene-order conservation score", "Wild yak Whole-genome alignment coverage", 
          "Wild yak orthology confidence [0 low, 1 high]", "Yarkand deer gene stable ID", 
          "Yarkand deer gene name", "Yarkand deer protein or transcript stable ID", 
          "Yarkand deer chromosome/scaffold name", "Yarkand deer chromosome/scaffold start (bp)", 
          "Yarkand deer chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Yarkand deer", "Yarkand deer homology type", 
          "%id. target Yarkand deer gene identical to query gene", 
          "%id. query gene identical to target Yarkand deer gene", 
          "Yarkand deer Gene-order conservation score", "Yarkand deer Whole-genome alignment coverage", 
          "Yarkand deer orthology confidence [0 low, 1 high]", 
          "Yellowtail amberjack gene stable ID", "Yellowtail amberjack gene name", 
          "Yellowtail amberjack protein or transcript stable ID", 
          "Yellowtail amberjack chromosome/scaffold name", "Yellowtail amberjack chromosome/scaffold start (bp)", 
          "Yellowtail amberjack chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Yellowtail amberjack", 
          "Yellowtail amberjack homology type", "%id. target Yellowtail amberjack gene identical to query gene", 
          "%id. query gene identical to target Yellowtail amberjack gene", 
          "Yellowtail amberjack Gene-order conservation score", 
          "Yellowtail amberjack Whole-genome alignment coverage", 
          "Yellowtail amberjack orthology confidence [0 low, 1 high]", 
          "Zebra finch gene stable ID", "Zebra finch gene name", 
          "Zebra finch protein or transcript stable ID", "Zebra finch chromosome/scaffold name", 
          "Zebra finch chromosome/scaffold start (bp)", "Zebra finch chromosome/scaffold end (bp)", 
          "Query protein or transcript ID", "Last common ancestor with Zebra finch", 
          "Zebra finch homology type", "%id. target Zebra finch gene identical to query gene", 
          "%id. query gene identical to target Zebra finch gene", 
          "Zebra finch Gene-order conservation score", "Zebra finch Whole-genome alignment coverage", 
          "Zebra finch orthology confidence [0 low, 1 high]", "Zebra mbuna gene stable ID", 
          "Zebra mbuna gene name", "Zebra mbuna protein or transcript stable ID", 
          "Zebra mbuna chromosome/scaffold name", "Zebra mbuna chromosome/scaffold start (bp)", 
          "Zebra mbuna chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Zebra mbuna", "Zebra mbuna homology type", 
          "%id. target Zebra mbuna gene identical to query gene", 
          "%id. query gene identical to target Zebra mbuna gene", 
          "Zebra mbuna Gene-order conservation score", "Zebra mbuna Whole-genome alignment coverage", 
          "Zebra mbuna orthology confidence [0 low, 1 high]", "Zebrafish gene stable ID", 
          "Zebrafish gene name", "Zebrafish protein or transcript stable ID", 
          "Zebrafish chromosome/scaffold name", "Zebrafish chromosome/scaffold start (bp)", 
          "Zebrafish chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Zebrafish", "Zebrafish homology type", 
          "%id. target Zebrafish gene identical to query gene", 
          "%id. query gene identical to target Zebrafish gene", 
          "Zebrafish Gene-order conservation score", "Zebrafish Whole-genome alignment coverage", 
          "Zebrafish orthology confidence [0 low, 1 high]", "Zig-zag eel gene stable ID", 
          "Zig-zag eel gene name", "Zig-zag eel protein or transcript stable ID", 
          "Zig-zag eel chromosome/scaffold name", "Zig-zag eel chromosome/scaffold start (bp)", 
          "Zig-zag eel chromosome/scaffold end (bp)", "Query protein or transcript ID", 
          "Last common ancestor with Zig-zag eel", "Zig-zag eel homology type", 
          "%id. target Zig-zag eel gene identical to query gene", 
          "%id. query gene identical to target Zig-zag eel gene", 
          "Zig-zag eel Gene-order conservation score", "Zig-zag eel orthology confidence [0 low, 1 high]", 
          "Human paralogue gene stable ID", "Human paralogue associated gene name", 
          "Human paralogue protein or transcript ID", "Human paralogue chromosome/scaffold name", 
          "Human paralogue chromosome/scaffold start (bp)", "Human paralogue chromosome/scaffold end (bp)", 
          "Paralogue query protein or transcript ID", "Paralogue last common ancestor with Human", 
          "Human paralogue homology type", "Paralogue %id. target Human gene identical to query gene", 
          "Paralogue %id. query gene identical to target Human gene", 
          "Gene stable ID", "Gene stable ID version", "Version (gene)", 
          "Transcript stable ID", "Transcript stable ID version", 
          "Version (transcript)", "Protein stable ID", "Protein stable ID version", 
          "Version (protein)", "Chromosome/scaffold name", "Gene start (bp)", 
          "Gene end (bp)", "Strand", "Karyotype band", "Gene name", 
          "Source of gene name", "Transcript count", "Gene % GC content", 
          "Gene description", "Variant name", "Variant source", 
          "Variant source description", "Variant alleles", "Variant supporting evidence", 
          "Mapweight", "Minor allele", "Minor allele frequency", 
          "Minor allele count", "Clinical significance", "Transcript location (bp)", 
          "Variant chromosome Strand", "Protein location (aa)", 
          "chromosome/scaffold position start (bp)", "Chromosome/scaffold position end (bp)", 
          "PolyPhen prediction", "PolyPhen score", "SIFT prediction", 
          "SIFT score", "Distance to transcript", "CDS start", 
          "CDS end", "Protein allele", "Variant consequence", "Consequence specific allele", 
          "Unspliced (Transcript)", "Unspliced (Gene)", "Flank (Transcript)", 
          "Flank (Gene)", "Flank-coding region (Transcript)", "Flank-coding region (Gene)", 
          "5' UTR", "3' UTR", "Exon sequences", "cDNA sequences", 
          "Coding sequence", "Peptide", "upstream_flank", "downstream_flank", 
          "Gene stable ID", "Gene stable ID version", "Gene description", 
          "Gene name", "Source of gene name", "Chromosome/scaffold name", 
          "Gene start (bp)", "Gene end (bp)", "Gene type", "Version (gene)", 
          "UniParc ID", "UniProtKB/Swiss-Prot ID", "UniProtKB/TrEMBL ID", 
          "CDS start (within cDNA)", "CDS end (within cDNA)", "5' UTR start", 
          "5' UTR end", "3' UTR start", "3' UTR end", "Transcript stable ID", 
          "Transcript stable ID version", "Protein stable ID", 
          "Protein stable ID version", "Transcript type", "Version (transcript)", 
          "Version (protein)", "Strand", "Transcript start (bp)", 
          "Transcript end (bp)", "Transcription start site (TSS)", 
          "Transcript length (including UTRs and CDS)", "CDS Length", 
          "CDS start", "CDS end", "Exon stable ID", "Exon region start (bp)", 
          "Exon region end (bp)", "Strand", "Exon rank in transcript", 
          "Start phase", "End phase", "cDNA coding start", "cDNA coding end", 
          "Genomic coding start", "Genomic coding end", "Constitutive exon"
          ), fullDescription = c("Stable ID of the Gene", "Versionned stable ID of the Gene", 
          "Stable ID of the Transcript", "Versionned stable ID of the Transcript", 
          "", "", "", "", "Chromosome/scaffold name", "Start Coordinate of the gene in chromosomal coordinates.", 
          "End Coordinate of the gene in chromosomal coordinates.", 
          "Orientation of genes on chromosome/scaffold.", "Band of chromosome/scaffold where genes occur.", 
          "Start Coordinate of the transcript in chromosomal coordinates.", 
          "End Coordinate of the gene in chromosomal coordinates.", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "Percentage gene GC content", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "InterPro Accession ID", 
          "InterPro Short Description", "InterPro Description", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "Snp Allele", "", "", 
          "", "", "", "", "Start of Variant on Transcript in Chromosomal Coordinates", 
          "Orientation of the SNP on the Transcript", "Location of the SNP in the peptide", 
          "Start of the Variant on the chromosome/scaffold in Chromosomal Coordinates", 
          "End of the Variant on the chromosome/scaffold in Chromosomal Coordinates", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", "", 
          "", "", "", "", "", "", "", "", "", "", "", "", "", ""
          ), page = c("feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "feature_page", "feature_page", "feature_page", "feature_page", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "structure", "structure", "structure", "structure", "structure", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "homologs", "homologs", "homologs", "homologs", 
          "homologs", "snp", "snp", "snp", "snp", "snp", "snp", 
          "snp", "snp", "snp", "snp", "snp", "snp", "snp", "snp", 
          "snp", "snp", "snp", "snp", "snp", "snp", "snp", "snp", 
          "snp", "snp", "snp", "snp", "snp", "snp", "snp", "snp", 
          "snp", "snp", "snp", "snp", "snp", "snp", "snp", "snp", 
          "snp", "snp", "snp", "snp", "snp", "snp", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences", "sequences", 
          "sequences", "sequences", "sequences", "sequences"), 
              attributes5 = c("html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", "html,txt,csv,tsv,xls", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta", 
              "fasta", "fasta", "fasta", "fasta", "fasta", "fasta"
              ), attributes6 = c("hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__translation__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__tra_tsl__dm", "hsapiens_gene_ensembl__tra_gencode_basic__dm", 
              "hsapiens_gene_ensembl__tra_appris__dm", "hsapiens_gene_ensembl__tra_is_canonical__dm", 
              "hsapiens_gene_ensembl__tra_mane_select__dm", "hsapiens_gene_ensembl__tra_mane_plus_clinical__dm", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__external_synonym__dm", 
              "hsapiens_gene_ensembl__phenotype__dm", "hsapiens_gene_ensembl__phenotype__dm", 
              "hsapiens_gene_ensembl__phenotype__dm", "hsapiens_gene_ensembl__phenotype__dm", 
              "hsapiens_gene_ensembl__phenotype__dm", "hsapiens_gene_ensembl__phenotype__dm", 
              "hsapiens_gene_ensembl__ontology_go__dm", "hsapiens_gene_ensembl__ontology_go__dm", 
              "hsapiens_gene_ensembl__ontology_go__dm", "hsapiens_gene_ensembl__ontology_go__dm", 
              "hsapiens_gene_ensembl__ontology_go__dm", "hsapiens_gene_ensembl__ox_goslim_goa__dm", 
              "hsapiens_gene_ensembl__ox_goslim_goa__dm", "hsapiens_gene_ensembl__ox_biogrid__dm", 
              "hsapiens_gene_ensembl__ox_ccds__dm", "hsapiens_gene_ensembl__ox_chembl__dm", 
              "hsapiens_gene_ensembl__ox_dbass3__dm", "hsapiens_gene_ensembl__ox_dbass3__dm", 
              "hsapiens_gene_ensembl__ox_dbass5__dm", "hsapiens_gene_ensembl__ox_dbass5__dm", 
              "hsapiens_gene_ensembl__ox_ens_hs_transcript__dm", 
              "hsapiens_gene_ensembl__ox_ens_hs_translation__dm", 
              "hsapiens_gene_ensembl__ox_entrezgene_trans_name__dm", 
              "hsapiens_gene_ensembl__ox_embl__dm", "hsapiens_gene_ensembl__ox_arrayexpress__dm", 
              "hsapiens_gene_ensembl__ox_genedb__dm", "hsapiens_gene_ensembl__ox_hgnc__dm", 
              "hsapiens_gene_ensembl__ox_hgnc__dm", "hsapiens_gene_ensembl__ox_hpa__dm", 
              "hsapiens_gene_ensembl__ox_hpa__dm", "hsapiens_gene_ensembl__ox_protein_id__dm", 
              "hsapiens_gene_ensembl__ox_ens_lrg_gene__dm", "hsapiens_gene_ensembl__ox_ens_lrg_transcript__dm", 
              "hsapiens_gene_ensembl__ox_merops__dm", "hsapiens_gene_ensembl__ox_mim_gene__dm", 
              "hsapiens_gene_ensembl__ox_mim_gene__dm", "hsapiens_gene_ensembl__ox_mim_morbid__dm", 
              "hsapiens_gene_ensembl__ox_mim_morbid__dm", "hsapiens_gene_ensembl__ox_mirbase__dm", 
              "hsapiens_gene_ensembl__ox_mirbase__dm", "hsapiens_gene_ensembl__ox_mirbase_trans_name__dm", 
              "hsapiens_gene_ensembl__ox_entrezgene__dm", "hsapiens_gene_ensembl__ox_entrezgene__dm", 
              "hsapiens_gene_ensembl__ox_entrezgene__dm", "hsapiens_gene_ensembl__ox_pdb__dm", 
              "hsapiens_gene_ensembl__ox_reactome__dm", "hsapiens_gene_ensembl__ox_reactome_gene__dm", 
              "hsapiens_gene_ensembl__ox_reactome_transcript__dm", 
              "hsapiens_gene_ensembl__ox_refseq_mrna__dm", "hsapiens_gene_ensembl__ox_refseq_mrna_predicted__dm", 
              "hsapiens_gene_ensembl__ox_refseq_ncrna__dm", "hsapiens_gene_ensembl__ox_refseq_ncrna_predicted__dm", 
              "hsapiens_gene_ensembl__ox_refseq_peptide__dm", "hsapiens_gene_ensembl__ox_refseq_peptide_predicted__dm", 
              "hsapiens_gene_ensembl__ox_rfam__dm", "hsapiens_gene_ensembl__ox_rfam_trans_name__dm", 
              "hsapiens_gene_ensembl__ox_rnacentral__dm", "hsapiens_gene_ensembl__ox_hgnc_trans_name__dm", 
              "hsapiens_gene_ensembl__ox_ucsc__dm", "hsapiens_gene_ensembl__ox_uniparc__dm", 
              "hsapiens_gene_ensembl__ox_uniprot_gn__dm", "hsapiens_gene_ensembl__ox_uniprot_gn__dm", 
              "hsapiens_gene_ensembl__ox_uniprot_isoform__dm", 
              "hsapiens_gene_ensembl__ox_uniprotswissprot__dm", 
              "hsapiens_gene_ensembl__ox_uniprotsptrembl__dm", 
              "hsapiens_gene_ensembl__ox_wikigene__dm", "hsapiens_gene_ensembl__ox_wikigene__dm", 
              "hsapiens_gene_ensembl__ox_wikigene__dm", "hsapiens_gene_ensembl__efg_affy_hc_g110__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_focus__dm", "hsapiens_gene_ensembl__efg_affy_hg_u133a__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_u133a_2__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_u133b__dm", "hsapiens_gene_ensembl__efg_affy_hg_u133_plus_2__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_u95a__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95av2__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_u95b__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95c__dm", 
              "hsapiens_gene_ensembl__efg_affy_hg_u95d__dm", "hsapiens_gene_ensembl__efg_affy_hg_u95e__dm", 
              "hsapiens_gene_ensembl__efg_affy_hta_2_0__dm", "hsapiens_gene_ensembl__efg_affy_huex_1_0_st_v2__dm", 
              "hsapiens_gene_ensembl__efg_affy_hugenefl__dm", "hsapiens_gene_ensembl__efg_affy_hugene_1_0_st_v1__dm", 
              "hsapiens_gene_ensembl__efg_affy_hugene_2_0_st_v1__dm", 
              "hsapiens_gene_ensembl__efg_affy_hugene_2_1_st_v1__dm", 
              "hsapiens_gene_ensembl__efg_affy_primeview__dm", 
              "hsapiens_gene_ensembl__efg_affy_u133_x3p__dm", "hsapiens_gene_ensembl__efg_agilent_cgh_44b__dm", 
              "hsapiens_gene_ensembl__efg_agilent_gpl26966__dm", 
              "hsapiens_gene_ensembl__efg_agilent_gpl6848__dm", 
              "hsapiens_gene_ensembl__efg_agilent_sureprint_g3_ge_8x60k__dm", 
              "hsapiens_gene_ensembl__efg_agilent_sureprint_g3_ge_8x60k_v2__dm", 
              "hsapiens_gene_ensembl__efg_agilent_wholegenome__dm", 
              "hsapiens_gene_ensembl__efg_agilent_wholegenome_4x44k_v1__dm", 
              "hsapiens_gene_ensembl__efg_agilent_wholegenome_4x44k_v2__dm", 
              "hsapiens_gene_ensembl__efg_codelink_codelink__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanht_12_v3__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanht_12_v4__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanref_8_v3__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v1__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v2__dm", 
              "hsapiens_gene_ensembl__efg_illumina_humanwg_6_v3__dm", 
              "hsapiens_gene_ensembl__efg_phalanx_onearray__dm", 
              "hsapiens_gene_ensembl__protein_feature_cdd__dm", 
              "hsapiens_gene_ensembl__protein_feature_cdd__dm", 
              "hsapiens_gene_ensembl__protein_feature_cdd__dm", 
              "hsapiens_gene_ensembl__protein_feature_gene3d__dm", 
              "hsapiens_gene_ensembl__protein_feature_gene3d__dm", 
              "hsapiens_gene_ensembl__protein_feature_gene3d__dm", 
              "hsapiens_gene_ensembl__protein_feature_hamap__dm", 
              "hsapiens_gene_ensembl__protein_feature_hamap__dm", 
              "hsapiens_gene_ensembl__protein_feature_hamap__dm", 
              "hsapiens_gene_ensembl__protein_feature_hmmpanther__dm", 
              "hsapiens_gene_ensembl__protein_feature_hmmpanther__dm", 
              "hsapiens_gene_ensembl__protein_feature_hmmpanther__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfam__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfam__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfam__dm", 
              "hsapiens_gene_ensembl__protein_feature_pirsf__dm", 
              "hsapiens_gene_ensembl__protein_feature_pirsf__dm", 
              "hsapiens_gene_ensembl__protein_feature_pirsf__dm", 
              "hsapiens_gene_ensembl__protein_feature_prints__dm", 
              "hsapiens_gene_ensembl__protein_feature_prints__dm", 
              "hsapiens_gene_ensembl__protein_feature_prints__dm", 
              "hsapiens_gene_ensembl__protein_feature_scanprosite__dm", 
              "hsapiens_gene_ensembl__protein_feature_scanprosite__dm", 
              "hsapiens_gene_ensembl__protein_feature_scanprosite__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfscan__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfscan__dm", 
              "hsapiens_gene_ensembl__protein_feature_pfscan__dm", 
              "hsapiens_gene_ensembl__protein_feature_sfld__dm", 
              "hsapiens_gene_ensembl__protein_feature_sfld__dm", 
              "hsapiens_gene_ensembl__protein_feature_sfld__dm", 
              "hsapiens_gene_ensembl__protein_feature_smart__dm", 
              "hsapiens_gene_ensembl__protein_feature_smart__dm", 
              "hsapiens_gene_ensembl__protein_feature_smart__dm", 
              "hsapiens_gene_ensembl__protein_feature_superfamily__dm", 
              "hsapiens_gene_ensembl__protein_feature_superfamily__dm", 
              "hsapiens_gene_ensembl__protein_feature_superfamily__dm", 
              "hsapiens_gene_ensembl__protein_feature_tigrfam__dm", 
              "hsapiens_gene_ensembl__protein_feature_tigrfam__dm", 
              "hsapiens_gene_ensembl__protein_feature_tigrfam__dm", 
              "hsapiens_gene_ensembl__interpro__dm", "hsapiens_gene_ensembl__interpro__dm", 
              "hsapiens_gene_ensembl__interpro__dm", "hsapiens_gene_ensembl__interpro__dm", 
              "hsapiens_gene_ensembl__interpro__dm", "hsapiens_gene_ensembl__protein_feature_mobidblite__dm", 
              "hsapiens_gene_ensembl__protein_feature_mobidblite__dm", 
              "hsapiens_gene_ensembl__protein_feature_mobidblite__dm", 
              "hsapiens_gene_ensembl__protein_feature_ncoils__dm", 
              "hsapiens_gene_ensembl__protein_feature_ncoils__dm", 
              "hsapiens_gene_ensembl__protein_feature_ncoils__dm", 
              "hsapiens_gene_ensembl__protein_feature_seg__dm", 
              "hsapiens_gene_ensembl__protein_feature_seg__dm", 
              "hsapiens_gene_ensembl__protein_feature_seg__dm", 
              "hsapiens_gene_ensembl__protein_feature_sifts_import__dm", 
              "hsapiens_gene_ensembl__protein_feature_sifts_import__dm", 
              "hsapiens_gene_ensembl__protein_feature_sifts_import__dm", 
              "hsapiens_gene_ensembl__protein_feature_signalp__dm", 
              "hsapiens_gene_ensembl__protein_feature_signalp__dm", 
              "hsapiens_gene_ensembl__protein_feature_signalp__dm", 
              "hsapiens_gene_ensembl__protein_feature_tmhmm__dm", 
              "hsapiens_gene_ensembl__protein_feature_tmhmm__dm", 
              "hsapiens_gene_ensembl__protein_feature_tmhmm__dm", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__exon_transcript__dm", "hsapiens_gene_ensembl__exon_transcript__dm", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__transcript__main", "hsapiens_gene_ensembl__transcript__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__translation__main", 
              "hsapiens_gene_ensembl__translation__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__gene__main", 
              "hsapiens_gene_ensembl__gene__main", "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_cabingdonii__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_scaustralis__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_mspretus__dm", "hsapiens_gene_ensembl__homolog_mspretus__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_vpacos__dm", "hsapiens_gene_ensembl__homolog_vpacos__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_mmmarmota__dm", "hsapiens_gene_ensembl__homolog_mmmarmota__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_pformosa__dm", "hsapiens_gene_ensembl__homolog_pformosa__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_bbbison__dm", "hsapiens_gene_ensembl__homolog_bbbison__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_uamericanus__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_nvison__dm", "hsapiens_gene_ensembl__homolog_nvison__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_cdromedarius__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_uparryii__dm", "hsapiens_gene_ensembl__homolog_uparryii__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_smerianae__dm", "hsapiens_gene_ensembl__homolog_smerianae__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_dnovemcinctus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_sformosus__dm", "hsapiens_gene_ensembl__homolog_sformosus__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_gmorhua__dm", 
              "hsapiens_gene_ensembl__homolog_gmorhua__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_charengus__dm", 
              "hsapiens_gene_ensembl__homolog_charengus__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_ssalar__dm", 
              "hsapiens_gene_ensembl__homolog_ssalar__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_cporosus__dm", 
              "hsapiens_gene_ensembl__homolog_cporosus__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lbergylta__dm", 
              "hsapiens_gene_ensembl__homolog_lbergylta__dm", "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_lcalcarifer__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_dleucas__dm", "hsapiens_gene_ensembl__homolog_dleucas__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_spartitus__dm", "hsapiens_gene_ensembl__homolog_spartitus__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_rbieti__dm", "hsapiens_gene_ensembl__homolog_rbieti__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_bmusculus__dm", "hsapiens_gene_ensembl__homolog_bmusculus__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_llaticaudata__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_sbboliviensis__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_ppaniscus__dm", "hsapiens_gene_ensembl__homolog_ppaniscus__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_strutta__dm", "hsapiens_gene_ensembl__homolog_strutta__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_hburtoni__dm", "hsapiens_gene_ensembl__homolog_hburtoni__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_ogarnettii__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_cintestinalis__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_csavignyi__dm", 
              "hsapiens_gene_ensembl__homolog_csavignyi__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_celegans__dm", 
              "hsapiens_gene_ensembl__homolog_celegans__dm", "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_ccapucinus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_fcatus__dm", "hsapiens_gene_ensembl__homolog_fcatus__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cwagneri__dm", "hsapiens_gene_ensembl__homolog_cwagneri__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_cgobio__dm", "hsapiens_gene_ensembl__homolog_cgobio__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ipunctatus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ggallus__dm", "hsapiens_gene_ensembl__homolog_ggallus__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_ptroglodytes__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_cgchok1gshd__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_osinensis__dm", "hsapiens_gene_ensembl__homolog_osinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_psinensis__dm", "hsapiens_gene_ensembl__homolog_psinensis__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_otshawytscha__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_atestudineus__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_aocellaris__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_lchalumnae__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_okisutch__dm", "hsapiens_gene_ensembl__homolog_okisutch__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_falbicollis__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_scanaria__dm", "hsapiens_gene_ensembl__homolog_scanaria__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_ccarpio__dm", "hsapiens_gene_ensembl__homolog_ccarpio__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_pmuralis__dm", "hsapiens_gene_ensembl__homolog_pmuralis__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_vursinus__dm", "hsapiens_gene_ensembl__homolog_vursinus__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_pcoquereli__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_btaurus__dm", "hsapiens_gene_ensembl__homolog_btaurus__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_mfascicularis__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_odegus__dm", "hsapiens_gene_ensembl__homolog_odegus__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_dclupeoides__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_cldingo__dm", "hsapiens_gene_ensembl__homolog_cldingo__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_clfamiliaris__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_ttruncatus__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_bgrunniens__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_eaasinus__dm", "hsapiens_gene_ensembl__homolog_eaasinus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_mleucophaeus__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_dmelanogaster__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_applatyrhynchos__dm", 
              "hsapiens_gene_ensembl__homolog_ptextilis__dm", "hsapiens_gene_ensembl__homolog_ptextilis__dm", 
              "hsapiens_gene_ensembl__homolog_ptextilis__dm", "hsapiens_gene_ensembl__homolog_ptextilis__dm", 
              "hsapiens_gene_ensembl__homolog_ptextilis__dm", "hsapiens_gene_ensembl__homolog_ptextilis__dm", 
              "hsapiens_gene_ensembl__homolog_ptextilis__dm", "hsapiens_gene_ensembl__homolog_ptextilis__dm", 
              "hsapiens_gene_ensembl__homolog_ptextilis__dm", "hsapiens_gene_ensembl__homolog_ptextilis__dm