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1. Carnitine palmitoyltransferase II deficiency

2. Cytochrome c oxidase deficiency

3. Glycogenosis type I

4. Glycogenosis 1 plus apoE2 type III hypertriglyceridemia

5. Hereditary dominant, with or without lysinuria; with or without pancreatic lithiasis or portal vein thrombosis

6. Homocystinuria

7. Hydroxymethylglutaryl-CoA lyase deficiency

8. Hyperlioproteinemia type IV

9. Isovaleric acidemia

10.Lipoprotein lipase deficiency, also type IV

11. Lysinuric protein intolerance

12. Maple syrup urine disease

13. MELAS

14. Methylmalonic acidemia

15. Ornithine transcarbamylase deficiency

16. Pearson syndrome

17. Propionic acidemia

18. Regional enteritis (Crohn)

19. Trauma-pseudocyst

20. With hyperparathyroidism in multiple endocrine adenomatosus syndrome