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1. Delta1-pyrroline-5-synthase deficiency

2. Cerebrotendinous xanthomatosis

3. Electron transport chain disorders

4. Fabry disease

5. Galactokinase deficiency

6. Galactosemia

7. Homocystinuria

8. Hyperferritinemia-cataract syndrome

9. Hyperornithinemia (ornithine aminotransferase deficiency)

10. Lowe syndrome

11. Lysinuric protein intolerance

12. Mannosidosis

13. Mevalonic aciduria

14. Multiple sulfatase deficiency

15. Neonatal carnitine palmitoyl transferase (CPT II deficiency)

16. α’-Pyrroline-5-carboxylate synthase deficiency

17. Peroxisomal disorders