OBO ID: DOID:0050534
Term Name: congenital stationary night blindness Search Ontology:
  • congenital essential nyctalopia
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. (5)
Ontology: Human Disease   (DOID:0050534)
OTHER congenital stationary night blindness PAGES
GENES INVOLVED No data available
PHENOTYPE No data available