Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

Log in / Sign up

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, 3 tagged with Usher syndrome type 1B itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Usher syndrome type 1 (3)

Including sub-types (3) Tagged with Usher syndrome type 1B (3)

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