Usher syndrome type 2D

Definition

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

Also known as USH2D, Usher syndrome caused by mutation in WHRN, Usher syndrome type 2D, WHRN Usher syndrome — per MONDO

Also identified as

• DOID 0110840 per MONDO
• OMIM 611383 per MONDO
• UMLS C1568249 per MONDO