DISEASES

Disease-gene associations mined from literature

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Human genes for catecholaminergic polymorphic ventricular tachycardia 3

Catecholaminergic polymorphic ventricular tachycardia 3 [DOID:0060677]

A catecholaminergic polymorphic ventricular tachycardia that is characterized by early onset mortality and has_material_basis_in variation in the chromosomal region 7p22-p14.

Synonyms:  catecholaminergic polymorphic ventricular tachycardia 3,  DOID:0060677,  CVPT3

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.