DISEASES

Disease-gene associations mined from literature

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Human genes for hypotrichosis 6

Hypotrichosis 6 [DOID:0110703]

A hypotrichosis that has_material_basis_in a autosomal recessive mutation of DSG4 on chromosome 18q12.1.

Synonyms:  hypotrichosis 6,  DOID:0110703,  autosomal recessive localized hypotrichosis,  Hypotrichosis, Localized, Autosomal Recessive 1,  Hypt6 ...

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.