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Summary Literature (0)
DOID:0111795 - congenital nystagmus 6

Disease Ontology Definition:A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in the GPR143 gene on chromosome Xp22.2.

Synonyms: NYS6, X-linked congenital nystagmus 6

Xenbase Genes : gpr143


MIM:
MIM:300814 - NYSTAGMUS 6, CONGENITAL, X-LINKED; NYS6

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital nystagmus (is_a)