DISEASES

Disease-gene associations mined from literature

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Human genes for X-linked exudative vitreoretinopathy 2

X-linked exudative vitreoretinopathy 2 [DOID:0111413]

An exudative vitreoretinopathy that has_material_basis_in mutation in NDP on chromosome Xp11.3.

Synonyms:  X-linked exudative vitreoretinopathy 2,  DOID:0111413,  Xlinked exudative vitreoretinopathy 2,  EVR2,  EVRX ...

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.