Disease-gene associations mined from literature

Human genes for congenital stationary night blindness

Congenital stationary night blindness [DOID:0050534]

A hereditary 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:  congenital stationary night blindness,  DOID:0050534,  congenital stationary night blindnesses,  congenital essential nyctalopia,  congenital essential nyctalopias

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