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Disease Ontology Browser
congenital stationary night blindness (DOID:0050534)
Synonyms: congenital essential nyctalopia
Alt IDs: OMIM:163500, OMIM:257270, OMIM:300071, OMIM:310500, OMIM:610427, OMIM:610444, OMIM:610445, OMIM:613216, OMIM:613830, OMIM:614565, OMIM:615058, OMIM:616389, ICD10CM:H53.63, ICD9CM:368.61, MESH:C537743, ORDO:215, UMLS_CUI:C1306122
Definition: A 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 (12)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory