DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for oculocutaneous albinism

Oculocutaneous albinism [DOID:0050632]

A syndrome characterized by abnormal pigmentation of the skin, hair and eyes.

Synonyms:  oculocutaneous albinism,  DOID:0050632,  oculocutaneous albinisms

Linkouts:  OMIM #1 #2 #3 #4 #5 #6

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.