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Usher syndrome type 1B

MONDO:0700087

Usher syndrome in which the cause of the disease is a mutation in the MYO7A gene

Also known as: Usher syndrome, type 1B

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

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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

New study aims to map vision decline in rare genetic disorder

Knowledge-focused Recruiting now

This study follows 60 people with Usher syndrome type 1B, a rare genetic condition causing deafness and progressive vision loss. Researchers will measure how vision changes over time using standard eye tests and new virtual reality tools. No treatment is given; the goal is to bet…

Sponsor: Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts • Aim: Knowledge-focused

Last updated Jun 27, 2026 09:03 UTC