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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.

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Sub-types

Usher syndrome type 1B (3) Usher syndrome type 1C (1) Usher syndrome type 1D (1) Usher syndrome type 1F (1) Usher syndrome type 1G (1) Usher syndrome, type 1D/F (0) Usher syndrome type 1E (0) Usher syndrome type 1H (0) Usher syndrome type 1K (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)
Trials to join now! 1 Not yet finished but already full! 2
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