RGD Annotation Report for autosomal recessive nonsyndromic deafness 4Rat Genome Database

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An association has been curated linking CV277681 and autosomal recessive nonsyndromic deafness 4 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
6 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 4 (DOID:0110498)
0 papers in RGD have been used to annotate CV277681
Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 4, with enlarged vestibular aqueduct

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