DISEASES

Disease-gene associations mined from literature

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Human genes for familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy [DOID:0080326]

A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.

Synonyms:  familial hypertrophic cardiomyopathy,  DOID:0080326,  hereditary hypertrophic cardiomyopathy,  familial hypertrophic cardiomyopathies

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.