DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for hypotrichosis 7

Hypotrichosis 7 [DOID:0110704]

A hypotrichosis that has_material_basis_in a autosomal recessive mutation of LIPH on chromosome 3q27.2.

Synonyms:  hypotrichosis 7,  DOID:0110704,  hypotrichosis, localized, autosomal recessive 2,  Hypt7,  Lah2 ...

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.