RGD Annotation Report for amelogenesis imperfecta type 3ARat Genome Database

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An association has been curated linking CV15820 and amelogenesis imperfecta type 3A 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
1 RGD objects have been annotated to amelogenesis imperfecta type 3A (DOID:0110055)
1 papers in RGD have been used to annotate CV15820
Curation Notes: ClinVar Annotator: match by term: AMELOGENESIS IMPERFECTA, TYPE IIIA
Original References(s): PMID:19407157

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