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Usher syndrome type 1

MONDO:0010168

A syndrome characterized by congenital, bilateral, severe sensorineural hearing loss, abnormalities in the vestibular system, and adolescent-onset retinitis pigmentosa.

Also known as: USH1, Usher syndrome type 1, Usher syndrome, type 1, retinitis pigmentosa and congenital deafness, USH1A, USHER syndrome, type I, Usher syndrome, type 1A, Usher syndrome, type 1B

3 clinical trials for this condition and its sub-types, 0 tagged with Usher syndrome type 1 itself.

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