Leber congenital amaurosis 7

MONDO:0013449

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

33 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by