RGD Annotation Report for oculocerebrorenal syndromeRat Genome Database

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An association has been curated linking CV743141 and oculocerebrorenal syndrome 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
15 RGD objects have been annotated to oculocerebrorenal syndrome (DOID:1056)
0 papers in RGD have been used to annotate CV743141
Curation Notes: ClinVar Annotator: match by term: Lowe syndrome
Original References(s): PMID:28492532

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