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DOID:0111796 - congenital nystagmus 5
Disease Ontology Definition:A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4.
Synonyms: NYS5, X-linked congenital nystagmus 5,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital nystagmus (is_a)