FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term Leber congenital amaurosis 19 ID (Ontology) DOID:0081169 (Human Disease)
Definition A Leber congenital amaurosis that has_material_basis_in mutation in the USP45 gene on chromosome 6q16.
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 Leber congenital amaurosis 19       1
 for disease ribbon | Leber congenital amaurosis 19       1
 model of | Leber congenital amaurosis 19       1
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retinal disease____|
                   Leber congenital amaurosis
                    |__Leber congenital amaurosis 19  1 rec.
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MIM:618513