Usher syndrome type 2A

Definition

Any Usher syndrome in which the cause of the disease is a mutation in the USH2A gene.

Also known as retinal disease in usher syndrome type IIA, modifier of, USH2A, USH2A Usher syndrome, Usher syndrome caused by mutation in USH2A, Usher syndrome type 2A — per MONDO

Also identified as

• DOID 0110838 per MONDO
• MESH C536490 per MONDO
• OMIM 276901 per MONDO
• UMLS C1848634 per MONDO