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Disease Ontology Browser
congenital stationary night blindness 1F (DOID:0110864)
Alliance: disease page
Synonyms: congenital stationary night blindness 1F autosomal recessive; CSNB1F
Alt IDs: OMIM:615058
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.

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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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory