DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy 13

Hypertrophic cardiomyopathy 13 [DOID:0110319]

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.

Synonyms:  hypertrophic cardiomyopathy 13,  DOID:0110319,  cardiomyopathy familial hypertrophic 13,  CMH13,  cardiomyopathy hereditary hypertrophic 13

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.