Ebstein Anomaly Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
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2 genes associated with the Ebstein Anomaly phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NKX2-5 NK2 homeobox 5