congenital nystagmus 2 Disease Ontology Browser

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Disease Ontology Browser

congenital nystagmus 2 (DOID:0111792)
Alliance: disease page
Synonyms: autosomal dominant congenital nystagmus 2; congenital motor nystagmus 2; NYS2
Alt IDs: OMIM:164100
Definition: A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.

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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