RGD Annotation Report for Familial Hyperaldosteronism, Type IIIRat Genome Database

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An association has been curated linking CV867573 and Familial Hyperaldosteronism, Type III 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
1 RGD objects have been annotated to Familial Hyperaldosteronism, Type III (DOID:9000644)
0 papers in RGD have been used to annotate CV867573
Curation Notes: ClinVar Annotator: match by term: FH III
Original References(s): PMID:22252394 PMID:23829355

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