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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126910289 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:30311386


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126744795 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11091011|RGD:8606685 (Homo sapiens) & RGD:11091011|RGD:8606685 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606681 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens) & RGD:13834871|RGD:150540669|RGD:150556502|RGD:151723810|RGD:151764861|RGD:156001796|RGD:156080273|RGD:156360321 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11094923 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:25741868


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152101802|RGD:152162217 (Homo sapiens) & RGD:152101802|RGD:152162217 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11089419|RGD:11091496 (Homo sapiens) & RGD:11089419|RGD:11091496 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266


    • An association has been curated linking TRIOBP and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens) & RGD:13531700|RGD:155645150|RGD:155909779|RGD:155909789|RGD:155916582|RGD:155923194|RGD:155930393|RGD:155935580|RGD:155942784|RGD:155948313|RGD:155975190|RGD:155981695|RGD:156007721|RGD:156056001|RGD:156095278|RGD:156171555|RGD:156288061|RGD:156337251|RGD:156342437|RGD:156342846|RGD:156367124|RGD:156369756|RGD:156379457|RGD:156387758|RGD:329367372|RGD:329367374|RGD:329393129|RGD:329401446 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate TRIOBP
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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