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Disease Ontology Browser
congenital stationary night blindness 1C (DOID:0110867)
Alliance: disease page
Synonyms: congenital stationary night blindness 1C autosomal recessive; CSNB1C
Alt IDs: OMIM:613216
Definition: A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14.


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
01/31/2023
MGI 6.22
The Jackson Laboratory