Leber congenital amaurosis 3 (MONDO_0011415, a Monarch Disease Ontology id) is any Leber congenital amaurosis in which the cause of the disease is a mutation in the SPATA7 gene. Also known as: LCA3, Leber congenital amaurosis caused by mutation in SPATA7, Leber congenital amaurosis type 3, SPATA7 Leber congenital amaurosis, retinitis pigmentosa, juvenile, autosomal recessive.