RGD Annotation Report for autosomal dominant Robinow syndrome 2Rat Genome Database

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An association has been curated linking CV217242 and autosomal dominant Robinow syndrome 2 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
5 RGD objects have been annotated to autosomal dominant Robinow syndrome 2 (DOID:0060765)
1 papers in RGD have been used to annotate CV217242
Curation Notes: ClinVar Annotator: match by term: Autosomal dominant Robinow syndrome 2
Original References(s): PMID:23806086 PMID:24088041 PMID:25741868 PMID:26924530

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