Leber congenital amaurosis 7
MONDO:0013449Any 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.
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