RGD Annotation Report for congenital disorder of glycosylation ImRat Genome Database

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An association has been curated linking CV316752 and congenital disorder of glycosylation Im 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
2 RGD objects have been annotated to congenital disorder of glycosylation Im (DOID:0080565)
0 papers in RGD have been used to annotate CV316752
Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1M

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