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Disease Ontology Browser
congenital nystagmus 3 (DOID:0111793)
Alliance: disease page
Synonyms: autosomal dominant congenital nystagmus 3; NYS3
Alt IDs: OMIM:608345
Definition: A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 7p11.2.

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
11/05/2024
MGI 6.24 		The Jackson Laboratory