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Summary Literature (0)
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,

Xenbase Genes : myo7a, ush2a, whrn, adgrv1, pdzd7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016484 - Usher syndrome type 2


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

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