DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for retinitis pigmentosa 37

Retinitis pigmentosa 37 [DOID:0110399]

A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.

Synonyms:  retinitis pigmentosa 37,  DOID:0110399,  RP37

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.