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Usher syndrome type 3

Disease Summary
Associated Targets (5)
Tbio

4

Tchem

1


GARD Rare
Mondo Description A syndrome characterized by postlingual progressive hearing loss, abnormalities in the vestibular system, and onset of retinitis pigmentosa symptoms usually by the second decade of life.
Disease Ontology Description 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.
Mondo Term and Equivalent IDs
MONDO:0016485:  Usher syndrome type 3
GARD:0005442: 
NCIT:C126329: 
Orphanet:231183: 
UMLS:C1568248: