Usher syndrome type 3

MONDO:0016485

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.

Also known as: USH3, Usher syndrome type 3

0 clinical trials for this condition and its sub-types.

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Sub-types

Usher syndrome type 3A (0) Usher syndrome type 3B (0)

Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Human disease (14) Usher syndrome (12) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by body system or component (0) Disease by etiologic mechanism (0)

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