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1 Annotations Found.

An association has been curated linking Fga and Congenital Hypodysfibrinogenemia in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  • 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 from sequence orthology with FGA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 0 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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