Perimembranous Ventricular Septal Defect Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A ventricular septal defect that is confluent with and involves the membranous septum and is bordered by an atrioventricular valve, not including the type 3 VSDs. (Human Phenotype Ontology, HP_0011682)
External Link	https://www.disgenet.org/browser/0/1/0/C0344925
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Genes

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

Symbol	Name
ATRX	alpha thalassemia/mental retardation syndrome X-linked
BMP2	bone morphogenetic protein 2
CITED2	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
GATA4	GATA binding protein 4
GATA6	GATA binding protein 6
NFATC1	nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1
RAD21	RAD21 homolog (S. pombe)
WDFY3	WD repeat and FYVE domain containing 3
ZEB2	zinc finger E-box binding homeobox 2