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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
Xenbase Genes
:
trpm1,
grm6,
nyx,
sag,
gnb3,
pde6b,
rho,
slc24a1,
gpr179,
gnat1,
grk1,
cacna1f,
cabp4,
lrit3,
rho.2
| MONDO:0016293 - congenital stationary night blindness |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee