|
DOID:0111797 - autosomal recessive congenital nystagmus
Disease Ontology Definition:A congenital nystagmus characterized by autosomal recessive inheritance.
Synonyms: autosomal recessive congenital motor nystagmus,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee