Leber congenital amaurosis 10

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CEP290 gene.

Also known as CEP290 Leber congenital amaurosis, LCA10, Leber congenital amaurosis 10, Leber congenital amaurosis caused by mutation in CEP290, Leber congenital amaurosis type 10 — per MONDO

Also identified as

• DOID 0110291 per MONDO
• MESH C565720 per MONDO
• OMIM 611755 per MONDO
• UMLS C1857821 per MONDO