Leber congenital amaurosis 5

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LCA5 gene.

Also known as LCA5, LCA5 Leber congenital amaurosis, Leber congenital amaurosis 5, Leber congenital amaurosis caused by mutation in LCA5, Leber congenital amaurosis type 5 — per MONDO

Also identified as

• DOID 0110215 per MONDO
• MESH C536602 per MONDO
• OMIM 604537 per MONDO
• UMLS C1858301 per MONDO