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Optic Atrophy
1. ADP-ribosyl protein lyase deficiency
2. Adrenoleukodystrophy (ALD)
3. Biotinidase deficiency
4. Canavan disease
5. GM₁ gangliosidosis
6. Homocystinuria
7. Krabbe disease
8. Menkes disease
9. Methylmalonic acidemia
10. MERRF
11. Metachromatic leukodystrophy
12. 3-Methylglutaconic aciduria, type III (Costeff)
13. Mevalonic aciduria
14. Mitochondrial energy metabolism, defect in-including
15. Leber hereditary optic neuropathy (LHON)
16. Multiple sulfatase deficiency
17. NARP
18. Neonatal adrenoleukodystrophy
19. Propionic acidemia
20. Sandhoff disease
21. Tay-Sachs disease