Leber congenital amaurosis 15

MONDO:0013457

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, retinitis pigmentosa, juvenile, Tulp1-related

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 15 itself.

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↑ Leber congenital amaurosis (13)

Including sub-types (25) Tagged with Leber congenital amaurosis 15 (0)

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