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Disease Ontology Browser
congenital stationary night blindness (DOID:0050534)
Alliance: disease page
Synonyms: congenital essential nyctalopia
Alt IDs: ICD10CM:H53.63, ICD9CM:368.61, MESH:C537743, OMIM:PS310500, ORDO:215, UMLS_CUI:C1306122
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.

Disease References using Mouse Models (20)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory