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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

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