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1 Annotations Found.

An association has been curated linking Fgg 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 FGG (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 Fgg
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN HAIFA 1 | ClinVar Annotator: match by term: FIBRINOGEN TOKYO 2 | ClinVar Annotator: match by term: Hypodysfibrinogenemia
  • Original References(s): PMID:11344575 PMID:15632207 PMID:1733971 PMID:2512677 PMID:25741868 PMID:2617471 PMID:2971042 PMID:2976995 PMID:31064749 PMID:3337908 PMID:34355501 PMID:3563970 PMID:4002201 PMID:6654188 PMID:6886002 PMID:7635941

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