DISEASES

Disease-gene associations mined from literature

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Human genes for ventricular septal defect

Ventricular septal defect [DOID:1657]

A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles.

Synonyms:  ventricular septal defect,  DOID:1657,  ventricular septal defects,  Interventricular septal defect,  Ventricular septal abnormality ...

Linkouts:  OMIM #1 #2 #3

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.