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1 Annotations Found.

An association has been curated linking Fgb and Congenital Hypodysfibrinogenemia in Chinchilla lanigera.        

  • 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 FGB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 2 papers in RGD have been used to annotate Fgb
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN BALTIMORE 2 | ClinVar Annotator: match by term: FIBRINOGEN CHRISTCHURCH 2 | ClinVar Annotator: match by term: FIBRINOGEN LONGMONT
  • Original References(s): PMID:11468164 PMID:1565641 PMID:25741868 PMID:31064749 PMID:3194892

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