DISEASES

Disease-gene associations mined from literature

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Human genes for arrhythmogenic right ventricular dysplasia 2

Arrhythmogenic right ventricular dysplasia 2 [DOID:0110071]

An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the cardiac ryanodine receptor-2 gene (RYR2) on chromosome 1q43.

Synonyms:  arrhythmogenic right ventricular dysplasia 2,  DOID:0110071,  arrhythmogenic right ventricular cardiomyopathy 2,  ARVC2,  ARVD2 ...

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.