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congenital stationary night blindness autosomal dominant 2 (DOID:0110863)
Alliance: disease page
Synonyms: CSNBAD2; Rambusch type congenital stationary night blindness
Alt IDs: OMIM:163500
Definition: A congenital stationary night blindness characterized by autosomal dominant inhertance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16.

Disease References using Mouse Models (3)

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
MGI 6.19
The Jackson Laboratory