Disease-gene associations mined from literature

Human genes for exudative vitreoretinopathy

Exudative vitreoretinopathy [DOID:0050535]

A night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.

Synonyms:  exudative vitreoretinopathy,  DOID:0050535,  familial exudative vitreoretinopathy,  FEVR,  hereditary exudative vitreoretinopathy

Linkouts:  OMIM #1 #2 #3 #4 #5