Pages that link to "Ornithine translocase deficiency"

The following pages link to Ornithine translocase deficiency:

Displayed 40 items.

• Tyrosinemia ‎ (← links)
• Trimethylaminuria ‎ (← links)
• Vision loss ‎ (← links)
• Glutathione synthetase deficiency ‎ (← links)
• Guanidinoacetate methyltransferase deficiency ‎ (← links)
• Hyperlysinemia ‎ (← links)
• Hypermethioninemia ‎ (← links)
• Hyperprolinemia ‎ (← links)
• Isobutyryl-coenzyme A dehydrogenase deficiency ‎ (← links)
• Prolidase deficiency ‎ (← links)
• Sarcosinemia ‎ (← links)
• Succinic semialdehyde dehydrogenase deficiency ‎ (← links)
• Urea cycle disorder ‎ (← links)
• Ornithine translocase ‎ (← links)
• Inborn error of metabolism ‎ (← links)
• Urea cycle ‎ (← links)
• HHH syndrome (redirect page) ‎ (← links)
  • List of diseases (H) ‎ (← links)
  • Newborn screening ‎ (← links)
  • Hepatitis causes ‎ (← links)
• Hyperammonemia ‎ (← links)
• Methylmalonyl-CoA mutase deficiency ‎ (← links)
• Translocase ‎ (← links)
• Inborn errors of renal tubular transport ‎ (← links)
• Hypervalinemia ‎ (← links)
• Organic acidemia ‎ (← links)
• Carnosinemia ‎ (← links)
• Hawkinsinuria ‎ (← links)
• Inborn errors of amino acid metabolism ‎ (← links)
• D-Glyceric acidemia ‎ (← links)
• Urocanic aciduria ‎ (← links)
• Amino acid transport disorder ‎ (← links)
• Argininemia ‎ (← links)
• 2-Hydroxyglutaric aciduria ‎ (← links)
• Hyperonithinemia-Hyperammonemia-Homocitrullinuria syndrome (redirect page) ‎ (← links)
• Type I tyrosinemia ‎ (← links)
• Type II tyrosinemia ‎ (← links)
• Type III tyrosinemia ‎ (← links)
• Disequilibrium causes ‎ (← links)
• Hyperonithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome (redirect page) ‎ (← links)
• 2-methylbutyryl-coenzyme a dehydrogenase deficiency ‎ (← links)
• Hypertryptophanemia ‎ (← links)
• Template:Amino acid metabolic pathology ‎ (← links)