Pages that link to "Propionic acidemia"

The following pages link to Propionic acidemia:

Displaying 50 items.

• Disease (← links | edit)
• List of diseases (H) (← links | edit)
• Genetic disorder (← links | edit)
• Homocystinuria (← links | edit)
• Pediatric glossary of terms (← links | edit)
• Pediatric glossary of terms expanded (← links | edit)
• Beta-ketothiolase deficiency (← links | edit)
• Fanconi syndrome (← links | edit)
• Isovaleric acidemia (← links | edit)
• Waardenburg syndrome (← links | edit)
• Carglumic acid (← links | edit)
• Inborn errors of metabolism (← links | edit)
• Cystinuria (← links | edit)
• Histidinemia (← links | edit)
• Fumarase deficiency (← links | edit)
• Health topics a-z (← links | edit)
• Carnitine-acylcarnitine translocase deficiency (← links | edit)
• Sjögren–Larsson syndrome (← links | edit)
• Very long-chain acyl-coenzyme A dehydrogenase deficiency (← links | edit)
• List of rare diseases-P (← links | edit)
• List of rare metabolic disorders (← links | edit)
• Health-encyclopedia-P (← links | edit)
• Diseases-and-disorders-P (← links | edit)
• Biotinidase deficiency (← links | edit)
• Saccharopinuria (← links | edit)
• Organic acidemia (← links | edit)
• Lysinuric protein intolerance (← links | edit)
• Ethylmalonic encephalopathy (← links | edit)
• Dopamine beta hydroxylase deficiency (← links | edit)
• Carnosinemia (← links | edit)
• Alkaptonuria (← links | edit)
• Acute fatty liver of pregnancy (← links | edit)
• Newborn screening (← links | edit)
• Homocystinuria due to CBS deficiency (← links | edit)
• Mild phenylketonuria (← links | edit)
• Myopathic carnitine deficiency (← links | edit)
• Carbamoyl phosphate synthetase 1 deficiency (← links | edit)
• Hermansky Pudlak syndrome 2 (← links | edit)
• Prolidase deficiency (← links | edit)
• 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (← links | edit)
• Glutaric aciduria type 1 (← links | edit)
• Inborn errors of renal tubular transport (← links | edit)
• Isobutyryl-coenzyme A dehydrogenase deficiency (← links | edit)
• Methylmalonyl-CoA mutase deficiency (← links | edit)
• Succinic semialdehyde dehydrogenase deficiency (← links | edit)
• Medium-chain acyl-coenzyme A dehydrogenase deficiency (← links | edit)
• 3-alpha hydroxyacyl-CoA dehydrogenase deficiency (← links | edit)
• 2-methylbutyryl-CoA dehydrogenase deficiency (← links | edit)
• 3-methylglutaconyl-CoA hydratase deficiency (AUH defect) (← links | edit)
• Carnitine palmitoyl transferase 1A deficiency (← links | edit)