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1 Annotations Found.

An association has been curated linking FGA and Congenital Hypodysfibrinogenemia 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:8565606 (Homo sapiens)
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 40 papers in RGD have been used to annotate FGA
  • Curation Notes: ClinVar Annotator: match by term: Hypodysfibrinogenemia, congenital
  • Original References(s): PMID:10891444 PMID:14615374 PMID:25741868 PMID:31064749

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