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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV31401 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
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 0 papers in RGD have been used to annotate CV31401
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN HAIFA 1
  • Original References(s): PMID:1733971 PMID:2512677 PMID:25741868 PMID:2976995 PMID:31064749 PMID:34355501 PMID:3563970 PMID:6654188


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