DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy 15

Hypertrophic cardiomyopathy 15 [DOID:0110321]

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the vinculin gene (VCL) on chromosome 10q22.

Synonyms:  hypertrophic cardiomyopathy 15,  DOID:0110321,  cardiomyopathy familial hypertrophic 15,  CMH15,  cardiomyopathy hereditary hypertrophic 15

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.