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

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 7 itself.

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↑ Leber congenital amaurosis (13) ↑ CRX-related retinopathy (0)

Including sub-types (25) Tagged with Leber congenital amaurosis 7 (0)

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