DISEASES

Disease-gene associations mined from literature

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Human genes for dyschromatosis symmetrica hereditaria

Dyschromatosis symmetrica hereditaria [DOID:0060257]

A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities.

Synonyms:  dyschromatosis symmetrica hereditaria,  DOID:0060257,  dyschromatosis symmetrica hereditarias,  reticulate acropigmentation of Dohi,  reticulate acropigmentation of Dohis

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.