DISEASES

Disease-gene associations mined from literature

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Human genes for Leber congenital amaurosis 12

Leber congenital amaurosis 12 [DOID:0110080]

A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.

Synonyms:  Leber congenital amaurosis 12,  DOID:0110080,  LCA12

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.