DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy 3

Hypertrophic cardiomyopathy 3 [DOID:0110309]

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.

Synonyms:  hypertrophic cardiomyopathy 3,  DOID:0110309,  cardiomyopathy familial hypertrophic 3,  CMH3,  cardiomyopathy hereditary hypertrophic 3

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.