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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking PDGFRA 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:12890047 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 46 papers in RGD have been used to annotate PDGFRA
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking PDGFRA 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:156165974|RGD:156389728|RGD:401738093 (Homo sapiens) & RGD:156165974|RGD:156389728|RGD:401738093 (Homo sapiens) & RGD:156165974|RGD:156389728|RGD:401738093 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 46 papers in RGD have been used to annotate PDGFRA
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking PDGFRA 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:11347598|RGD:13819989|RGD:14706842|RGD:14737108|RGD:155750010 (Homo sapiens) & RGD:11347598|RGD:13819989|RGD:14706842|RGD:14737108|RGD:155750010 (Homo sapiens) & RGD:11347598|RGD:13819989|RGD:14706842|RGD:14737108|RGD:155750010 (Homo sapiens) & RGD:11347598|RGD:13819989|RGD:14706842|RGD:14737108|RGD:155750010 (Homo sapiens) & RGD:11347598|RGD:13819989|RGD:14706842|RGD:14737108|RGD:155750010 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 46 papers in RGD have been used to annotate PDGFRA
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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