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Disease Ontology Browser
congenital stationary night blindness 1G (DOID:0110714)
Alliance: disease page
Synonyms: congenital stationary night blindness type 1G; CSNB1G
Alt IDs: OMIM:616389
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous 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)
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last database update
07/05/2024
MGI 6.24
The Jackson Laboratory