Leber congenital amaurosis 8

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene.

Also known as CRB1 Leber congenital amaurosis, LCA8, Leber congenital amaurosis 8, Leber congenital amaurosis caused by mutation in CRB1, Leber congenital amaurosis type 8 — per MONDO

Also identified as

• DOID 0110079 per MONDO
• OMIM 613835 per MONDO
• UMLS C3151202 per MONDO