DISEASES

Disease-gene associations mined from literature

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Human genes for bradyopsia

Bradyopsia [DOID:0050335]

A retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes.

Synonyms:  bradyopsia,  DOID:0050335,  bradyopsias,  prolonged electroretinal response suppression,  prolonged electroretinal response suppressions

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.