Ventricular Septal Defect Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles. (Human Disease Ontology, DOID_1657)
External Link https://www.disgenet.org/browser/0/1/0/C0018818
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Genes

3 genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
GATA4 GATA binding protein 4
NKX2-5 NK2 homeobox 5