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1.  α-1-Antitrypsin deficiency

2. Fatty acid oxidation disorders

3. Galactosemia

4. Hepatorenal tyrosinemia

5. Hereditary fructose intolerance

6. Mitochondrial depletion syndromes, esp. POLGI and MPV17 mutations

7. Neonatal hemochromatosis

8. Niemann-Pick types B and C

9. Urea cycle disorders

10. Wilson disease

11. Wolcott-Rallison syndrome