Leber congenital amaurosis 13

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RDH12 gene.

Also known as LCA13, Leber congenital amaurosis 13, Leber congenital amaurosis caused by mutation in RDH12, Leber congenital amaurosis type 13, RDH12 Leber congenital amaurosis — per MONDO

Also identified as

• DOID 0110330 per MONDO
• MESH C567197 per MONDO
• OMIM 612712 per MONDO
• UMLS C2675186 per MONDO