DISEASES

Disease-gene associations mined from literature

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Human genes for refractive amblyopia

Refractive amblyopia [DOID:10377]

An amblyopia that is characterized by refractive error in one or both eyes that is not corrected early in childhood resulting in poor development of the visual function in the affected eye(s).

Synonyms:  refractive amblyopia,  DOID:10377,  refractive amblyopias,  ametropic amblyopia,  ametropic amblyopias

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.