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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 (18)

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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last database update
05/17/2022
MGI 6.19
The Jackson Laboratory