DISEASES

Disease-gene associations mined from literature

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Human genes for X-linked juvenile retinoschisis 1

X-linked juvenile retinoschisis 1 [DOID:0060763]

A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that has_material_basis_in the RS1 gene on chromosome Xp22.

Synonyms:  X-linked juvenile retinoschisis 1,  DOID:0060763,  Xlinked juvenile retinoschisis 1,  X-linked juvenile retinoschisis,  X-linked retinoschisis ...

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.