Misplaced Pages

The following pages link to Glutaric acidemia type 2

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Showing 50 items.

• Phenylketonuria (links | edit)
• Riboflavin (links | edit)
• Adrenoleukodystrophy (links | edit)
• List of genetic disorders (links | edit)
• Alkaptonuria (links | edit)
• Methylmalonic acidemias (links | edit)
• Propionic acidemia (links | edit)
• Hyperammonemia (links | edit)
• Medium-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
• Waardenburg syndrome (links | edit)
• Homocystinuria (links | edit)
• Cystinuria (links | edit)
• Ornithine transcarbamylase deficiency (links | edit)
• Inborn errors of metabolism (links | edit)
• Fatty acid metabolism (links | edit)
• Flavin adenine dinucleotide (links | edit)
• Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (links | edit)
• Trimethylaminuria (links | edit)
• Isovaleric acidemia (links | edit)
• Maple syrup urine disease (links | edit)
• Cystinosis (links | edit)
• Citrullinemia (links | edit)
• Beta-ketothiolase deficiency (links | edit)
• 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
• Tyrosinemia (links | edit)
• Beta oxidation (links | edit)
• Systemic primary carnitine deficiency (links | edit)
• Multiple acyl-CoA dehydrogenation deficiency (redirect page) (links | edit)
• Inborn error of lipid metabolism (links | edit)
• Hartnup disease (links | edit)
• Glutaric aciduria type 1 (links | edit)
• Carnitine palmitoyltransferase I deficiency (links | edit)
• Carnitine palmitoyltransferase II deficiency (links | edit)
• Saccharopinuria (links | edit)
• Carnitine-acylcarnitine translocase deficiency (links | edit)
• Mitochondrial trifunctional protein deficiency (links | edit)
• Very long-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
• Ochronosis (links | edit)
• Lysinuric protein intolerance (links | edit)
• Hyperlysinemia (links | edit)
• Biotinidase deficiency (links | edit)
• Tetrahydrobiopterin deficiency (links | edit)
• Hermansky–Pudlak syndrome (links | edit)
• Argininosuccinic aciduria (links | edit)
• Oculocutaneous albinism (links | edit)
• Glutaric acidemia type II (redirect page) (links | edit)
  • ETFA (links | edit)
  • ETFB (links | edit)
  • List of disorders included in newborn screening programs (links | edit)
• Electron transfer flavoprotein deficiency (redirect page) (links | edit)
• ETFA deficiency (redirect page) (links | edit)
• ETFB deficiency (redirect page) (links | edit)
• ETFDH deficiency (redirect page) (links | edit)