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Disease Ontology Browser
congenital stationary night blindness 1D (DOID:0110868)
Synonyms: congenital stationary night blindness 1D autosomal recessive; CSNB1D
Alt IDs: OMIM:613830
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
07/11/2017
MGI 6.10 		The Jackson Laboratory