DISEASES

Disease-gene associations mined from literature

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Human genes for Argyll Robertson pupil

Argyll Robertson pupil [DOID:14523]

An abnormal pupillary function characterized by a small pupil, the absence of a pupillary light reflex and the retention of a normal pupillary near response.

Synonyms:  Argyll Robertson pupil,  Argyll Robertson pupils,  DOID:14523,  Argyll Robertson phenomenon or pupil, nonsyphilitic,  Argyll Robertson pupil, atypical ...

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.