Usher syndrome type 3B

Definition

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 — per MONDO

Also identified as

• DOID 0110842 per MONDO
• OMIM 614504 per MONDO
• UMLS C3281066 per MONDO