RGD Annotation Report for HypofibrinogenemiaRat Genome Database

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An association has been curated linking CV31430 and Hypofibrinogenemia 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
41 RGD objects have been annotated to Hypofibrinogenemia (HP:0011900)
0 papers in RGD have been used to annotate CV31430
Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
Original References(s): PMID:11468164 PMID:25741868 PMID:31064749

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.