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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking FTHL17 and Duchenne muscular dystrophy 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:40903597 (Homo sapiens)
  • 43 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 2 papers in RGD have been used to annotate FTHL17
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


    • An association has been curated linking FTHL17 and Duchenne muscular dystrophy 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:156439456 (Homo sapiens)
  • 43 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 2 papers in RGD have been used to annotate FTHL17
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12632325 PMID:19937601 PMID:24302611 PMID:28492532


    • An association has been curated linking FTHL17 and Duchenne muscular dystrophy 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:156438285 (Homo sapiens)
  • 43 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 2 papers in RGD have been used to annotate FTHL17
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12632325 PMID:28492532 PMID:31705731


    • An association has been curated linking FTHL17 and Duchenne muscular dystrophy 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:127271127 (Homo sapiens)
  • 43 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 2 papers in RGD have been used to annotate FTHL17
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:22510846 PMID:23453023 PMID:24504883 PMID:28492532


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