Usher syndrome type 3B

MONDO:0013788

Any Usher syndrome in which the cause of the disease is a mutation in the HARS gene.

Also known as: HARS Usher syndrome, USH3B, Usher syndrome caused by mutation in HARS, USHER syndrome, type IIIB, Usher syndrome, type 3B

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

Follow this condition — get notified about new trials

Broader categories

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.