About   Help   FAQ
Disease Ontology Browser
congenital stationary night blindness autosomal dominant 1 (DOID:0110862)
Alliance: disease page
Synonyms: CSNBAD1; rhodopsin-related congenital stationary night blindness
Alt IDs: OMIM:610445
Definition: A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.

Disease References using Mouse Models (1)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory