Leber congenital amaurosis 11

MONDO:0013454

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene.

Also known as: IMPDH1 Leber congenital amaurosis, LCA11, Leber congenital amaurosis 11, Leber congenital amaurosis caused by mutation in IMPDH1, Leber congenital amaurosis type 11, amaurosis congenita of Leber, type 11

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