RGD Annotation Report for Rod-cone dystrophyRat Genome Database

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An association has been curated linking CV890296 and Rod-cone dystrophy 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
402 RGD objects have been annotated to Rod-cone dystrophy (HP:0000510)
0 papers in RGD have been used to annotate CV890296
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa

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