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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)
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04/09/2024
MGI 6.23 		The Jackson Laboratory