DISEASES

Disease-gene associations mined from literature

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Human genes for Cogan-Reese syndrome

Cogan-Reese syndrome [DOID:0060217]

An eye disease characterized by variable iris atrophy, pigmented and pedunculated nodules located_in iris and attachment of the iris to the cornea (peripheral anterior synechiae) and characterized_by glaucoma.

Synonyms:  Cogan-Reese syndrome,  CoganReese syndrome,  Cogan-Reese disease,  Cogan-Reese disorder,  Cogan-Reese 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.