DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy 20

Hypertrophic cardiomyopathy 20 [DOID:0110326]

A familial hypertrophic cardiomyopathy that hhas_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.

Synonyms:  hypertrophic cardiomyopathy 20,  DOID:0110326,  cardiomyopathy familial hypertrophic 20,  CMH20,  cardiomyopathy hereditary hypertrophic 20

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.