RGD Annotation Report for Esophageal atresiaRat Genome Database

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An association has been curated linking PDE2A and Esophageal atresia 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:15174110 (Homo sapiens)
143 RGD objects have been annotated to Esophageal atresia (HP:0002032)
9 papers in RGD have been used to annotate PDE2A
Curation Notes: ClinVar Annotator: match by term: Esophageal atresia

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