DISEASES

Disease-gene associations mined from literature

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Human genes for pigment dispersion syndrome

Pigment dispersion syndrome [DOID:0060680]

An eye disease characterized by slit-like depigmented areas of the iris with up to 50% of patients going on to develop glaucoma.

Synonyms:  pigment dispersion syndrome,  DOID:0060680,  pigment dispersion disease,  pigment dispersion disorder,  pigment dispersion syndromes ...

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.