DISEASES

Disease-gene associations mined from literature

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Human genes for congenital nystagmus 7

Congenital nystagmus 7 [DOID:0111791]

A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 1q31.3-q32.1.

Synonyms:  congenital nystagmus 7,  DOID:0111791,  autosomal dominant congenital nystagmus 7,  NYS7

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.