RGD Annotation Report for autosomal recessive limb-girdle muscular dystrophy type 2JRat Genome Database

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An association has been curated linking CV286101 and autosomal recessive limb-girdle muscular dystrophy type 2J 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
23 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2J (DOID:0110283)
0 papers in RGD have been used to annotate CV286101
Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2J

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