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Echinobase
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,

Echinobase Genes : whrn, ush2a, adgrv1



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)