congenital nystagmus 2

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0111792 - congenital nystagmus 2

Disease Ontology Definition:A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.

Synonyms: NYS2, autosomal dominant congenital nystagmus 2, congenital motor nystagmus 2,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), congenital nystagmus (is_a)