IMPDH1 Leber congenital amaurosisLCA11Leber congenital amaurosis 11Leber congenital amaurosis caused by mutation in IMPDH1Leber congenital amaurosis type 11amaurosis congenita of Leber, type 11
Definition
Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene.
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