DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal dominant keratitis

Autosomal dominant keratitis [DOID:0111383]

A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in PAX6 on chromosome 11p13.

Synonyms:  autosomal dominant keratitis,  autosomal dominant keratitises,  DOID:0111383,  hereditary keratitis,  familial keratitis ...

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.