Usher syndrome type 1B

Definition

Usher syndrome in which the cause of the disease is a mutation in the MYO7A gene

Also known as Usher syndrome, type 1B — per MONDO

Also identified as

• DOID 0070655 per MONDO
• MESH C536485 per MONDO
• OMIM 276900 per MONDO
• UMLS C2931206 per MONDO