About   Help   FAQ
Disease Ontology Browser
congenital stationary night blindness autosomal dominant 3 (DOID:0110715)
Alliance: disease page
Synonyms: CSNBAD3; Nougaret type congenital stationary night blindness
Alt IDs: OMIM:610444
Definition: A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory