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ENLeber Congenital Amaurosis 5 (LCA5)
Alias:
Lca5
Leber Congenital Amaurosis, Type 5
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Leber Congenital Amaurosis 5, also known as lca5, is related to leber plus disease and fundus dystrophy. An important gene associated with Leber Congenital Amaurosis 5 is LCA5 (Lebercilin LCA5). Affiliated tissues include retina and eye, and related phenotypes are nystagmus and visual impairment
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