Ebstein Anomaly Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A tricuspid valve disease that is a congenital heart defect in which the septal leaflet of the tricuspid valve is displaced towards the apex of the right ventricle of the heart. (Human Disease Ontology, DOID_14289)
External Link	https://www.disgenet.org/browser/0/1/0/C0013481
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Genes

9 genes associated with the disease Ebstein Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AKAP12	A kinase (PRKA) anchor protein 12
BMPR1A	bone morphogenetic protein receptor, type IA
CDK8	cyclin-dependent kinase 8
CHDH	choline dehydrogenase
GATA4	GATA binding protein 4
MYH7	myosin, heavy chain 7, cardiac muscle, beta
NKX2-5	NK2 homeobox 5
NONO	non-POU domain containing, octamer-binding
TPM1	tropomyosin 1 (alpha)