DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for hypotrichosis 13

Hypotrichosis 13 [DOID:0110710]

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of KRT71 on chromosome 12q13.13.

Synonyms:  hypotrichosis 13,  DOID:0110710,  hypotrichosis with woolly hair,  Hypt13,  hypotrichosis with woolly hairs

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.