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An association has been curated linking CV2363333 and genetic disease 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
27153 RGD objects have been annotated to genetic disease (DOID:630)
0 papers in RGD have been used to annotate CV2363333
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:28492532

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