DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for hypomelanosis of Ito

Hypomelanosis of Ito [DOID:3156]

A skin disease that is characterized by distinctive skin changes, in which areas of the body lack skin color (hypopigmentation).

Synonyms:  hypomelanosis of Ito,  DOID:3156,  hypomelanosis of Itoes,  Bloch-Siemans syndrome,  incontinentia pigmenti achromians ...

Linkouts:  OMIM

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.