DISEASES

Disease-gene associations mined from literature

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Human genes for hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy [DOID:11984]

An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.

Synonyms:  hypertrophic cardiomyopathy,  DOID:11984,  hypertrophic cardiomyopathies,  hypertrophic obstructive cardiomyopathy,  hypertrophic obstructive cardiomyopathies

Linkouts:  OMIM #1 #2 #3 #4

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.