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Summary Literature (1)
DOID:0050439 - Usher syndrome

Disease Ontology Definition:A syndrome characterized by a combination of hearing loss and visual impairment.


Xenbase Genes : myo7a, ush2a, cdh23, cib2, pcdh15, whrn, adgrv1, ush1g, ush1c, cep78, clrn1, pdzd7, hars1, arsg

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019501 - Usher syndrome

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

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