DOID:0050534 - congenital stationary night blindness
Disease Ontology Definition: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 essential nyctalopia
|MONDO:0016293 - congenital stationary night blindness|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : trpm1, grm6, nyx, gnb3, pde6b, rho, slc24a1, gpr179, gnat1, cacna1f, cabp4, lrit3, rho.2
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD