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DOID:0111790 - congenital nystagmus 1
Disease Ontology Definition:A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2.
Synonyms: NYS1, X-linked infantile nystagmus 1, congenital motor nystagmus 1,
Xenbase Genes : frmd7
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee