Leber congenital amaurosis 2

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPE65 gene.

Also known as LCA2, Leber congenital amaurosis 2, Leber congenital amaurosis caused by mutation in RPE65, Leber congenital amaurosis type 2, RPE65 Leber congenital amaurosis — per MONDO

Also identified as

• DOID 0110016 per MONDO
• MESH C536601 per MONDO
• OMIM 204100 per MONDO
• UMLS C1859844 per MONDO