Usher syndrome type 3

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Summary

Literature (0)

DOID:0110828 - Usher syndrome type 3

Disease Ontology Definition:An Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life.

Synonyms: USH3

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cep78, clrn1, hars1, arsg

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0016485 - Usher syndrome type 3

MONDO:0016485 - Usher syndrome type 3

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)