DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy 7

Hypertrophic cardiomyopathy 7 [DOID:0110313]

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.

Synonyms:  hypertrophic cardiomyopathy 7,  DOID:0110313,  cardiomyopathy, familial hypertrophic 7,  CMH7,  cardiomyopathy familial hypertrophic 7 ...

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.