RGD Annotation Report for hereditary multiple exostosesRat Genome Database

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An association has been curated linking CV2524475 and hereditary multiple exostoses 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
36 RGD objects have been annotated to hereditary multiple exostoses (DOID:206)
0 papers in RGD have been used to annotate CV2524475
Curation Notes: ClinVar Annotator: match by term: Multiple congenital exostosis
Original References(s): PMID:17576681 PMID:19810120 PMID:23439489 PMID:28492532 PMID:9536098

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