DISEASES

Disease-gene associations mined from literature

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Human genes for Ebstein anomaly

Ebstein anomaly [DOID:14289]

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.

Synonyms:  Ebstein anomaly,  DOID:14289,  Ebstein anomalies,  Ebstein's anomaly,  Ebstein's anomaly of common atrioventricular valve ...

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.