|
DOID:0111793 - congenital nystagmus 3
Disease Ontology Definition:A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 7p11.2.
Synonyms: NYS3, autosomal dominant congenital nystagmus 3,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee