DISEASES

Disease-gene associations mined from literature

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Human genes for keratoconus

Keratoconus [DOID:10126]

A corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape.

Synonyms:  keratoconus,  DOID:10126,  keratoconuses,  keratoconi,  conical cornea ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9

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.