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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 (2)

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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last database update
11/15/2022
MGI 6.22
The Jackson Laboratory