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, congenital stationary night blindnesses, DOID:0050534, congenital essential nyctalopia, congenital essential nyctalopias
Linkouts: OMIM #1 #2 #3 #4 #5 #6 #7 #8