Usher syndrome type 3A

Definition

Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene.

Also known as CLRN1 Usher syndrome, USH3A, Usher syndrome caused by mutation in CLRN1, Usher syndrome type 3A — per MONDO

Also identified as

• DOID 0110841 per MONDO
• OMIM 276902 per MONDO
• UMLS C5779850 per MONDO