OBO ID: DOID:0050534 |
Term Name: | congenital stationary night blindness | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0050534 ) |
OTHER congenital stationary night blindness PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
PHENOTYPE
No data available
CITATIONS (3)
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