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DOID:0110827 - Usher syndrome type 2
Disease Ontology Definition:An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa.
Synonyms: USH2,
Echinobase Genes : whrn, ush2a, adgrv1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Usher syndrome (is_a)