DISEASES

Disease-gene associations mined from literature

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Human genes for MYH-9 related disease

MYH-9 related disease [DOID:0060651]

A blood platelet disease that has_material_basis_in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.

Synonyms:  MYH-9 related disease,  DOID:0060651,  MYH9 related disease,  MYH-9 related disorder,  MYH-9 related syndrome

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.