About   Help   FAQ
Disease Ontology Browser
congenital stationary night blindness 1B (DOID:0110865)
Alliance: disease page
Synonyms: autosomal recessive complete congenital stationary night blindness; congenital stationary night blindness 1B autosomal recessive; CSNB1B
Alt IDs: OMIM:257270
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.

Disease References using Mouse Models (3)
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
12/30/2025
MGI 6.24 		The Jackson Laboratory