Leber congenital amaurosis 15

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the TULP1 gene.

Also known as LCA15, Leber congenital amaurosis 15, Leber congenital amaurosis caused by mutation in TULP1, Leber congenital amaurosis type 15, TULP1 Leber congenital amaurosis — per MONDO

Also identified as

• DOID 0110189 per MONDO
• OMIM 613843 per MONDO
• UMLS C3151206 per MONDO