|OBO ID: DOID:0050534|
|Term Name:||congenital stationary night blindness||Search 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. (5)|
|Ontology:||Human Disease (DOID:0050534)|
|is a type of:||
OTHER congenital stationary night blindness PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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