DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for congenital nystagmus 4

Congenital nystagmus 4 [DOID:0111794]

A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 13q31-q33.

Synonyms:  congenital nystagmus 4,  DOID:0111794,  autosomal dominant congenital nystagmus 4,  NYS4,  vestibulocerebellar disorder with predominant ocular signs ...

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.