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congenital stationary night blindness autosomal dominant 3 (DOID:0110715)
Alliance: disease page
Synonyms: CSNBAD3; Nougaret type congenital stationary night blindness
Alt IDs: OMIM:610444
Definition: A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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The Jackson Laboratory