RGD Annotation Report for Ventricular septal defectRat Genome Database

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An association has been curated linking HOXA13 and Ventricular septal defect in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
504 RGD objects have been annotated to Ventricular septal defect (HP:0001629)
8 papers in RGD have been used to annotate HOXA13
Original References(s): ORPHA:2438

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