RGD Annotation Report for Leber congenital amaurosis 14Rat Genome Database

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An association has been curated linking CV890288 and Leber congenital amaurosis 14 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
2 RGD objects have been annotated to Leber congenital amaurosis 14 (DOID:0110188)
0 papers in RGD have been used to annotate CV890288
Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 14

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