Disease-gene associations mined from literature

Human genes for retinoschisis

Retinoschisis [DOID:8465]

Retinoschisis is an eye disease characterized by the abnormal splitting of the retina's neurosensory layers, usually in the outer plexiform layer, resulting in a loss of vision in the corresponding visual field in some rarer forms. More common forms are usually asymptomatic.

Synonyms:  retinoschisis,  DOID:8465,  Retinoschisis (disorder),  Retinoschisis unspecified (disorder),  Retinoschisis, unspecified ...

Linkouts:  OMIM #1 #2 #3