DISEASES

Disease-gene associations mined from literature

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Human genes for infantile histiocytoid cardiomyopathy

Infantile histiocytoid cardiomyopathy [DOID:0080198]

An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b.

Synonyms:  infantile histiocytoid cardiomyopathy,  DOID:0080198,  infantile histiocytoid 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.