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Disease Ontology Browser
congenital stationary night blindness 1A (DOID:0110870)
Alliance: disease page
Synonyms: complete CSNB X-linked; congenital stationary night blindness 1A X-linked; congenital stationary night blindness with myopia; CSNB1A; hemeralopia-myopia; myopia-night blindness; NBMI
Alt IDs: OMIM:310500
Definition: A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.

Disease References using Mouse Models (2)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory