congenital nystagmus 5 Disease Ontology Browser

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Disease Ontology Browser

congenital nystagmus 5 (DOID:0111796)
Alliance: disease page
Synonyms: NYS5; X-linked congenital nystagmus 5
Alt IDs: OMIM:300589
Definition: A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4.

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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