Leber congenital amaurosis 7

Definition

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

Also known as CRX Leber congenital amaurosis, LCA7, Leber congenital amaurosis 7, Leber congenital amaurosis caused by mutation in CRX, Leber congenital amaurosis type 7 — per MONDO

Also identified as

• DOID 0110333 per MONDO
• OMIM 613829 per MONDO
• UMLS C3151192 per MONDO