DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for dyschromatosis universalis hereditaria

Dyschromatosis universalis hereditaria [DOID:0060304]

A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.

Synonyms:  dyschromatosis universalis hereditaria,  DOID:0060304,  dyschromatosis universalis hereditarias

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.