RGD Annotation Report for Ehlers-Danlos syndromeRat Genome Database

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An association has been curated linking C1R and Ehlers-Danlos syndrome 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
The annotation has been inferred by association of genotype and phenotype with RGD:38462424 (Homo sapiens)
297 RGD objects have been annotated to Ehlers-Danlos syndrome (DOID:13359)
7 papers in RGD have been used to annotate C1R
Curation Notes: ClinVar Annotator: match by term: Ehlers-Danlos syndrome

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