OnlineIMD

4.2        Disorders of mitochondrial fatty acid oxidation

  • Type
    Group
  • Pathway
    • Carnitine metabolism and fatty acid oxidation
  • Disease group(s)
    • 4         Disorders of carnitine, mitochondrial fatty acid and ketone body metabolism
  • Child entries
    • Mitochondrial trifunctional protein deficiency
    • Very long-chain acyl-CoA dehydrogenase deficiency
    • Medium-chain acyl-CoA dehydrogenase deficiency
    • Medium-chain 3-ketoacyl-CoA thiolase deficiency
    • Short-chain acyl-CoA dehydrogenase deficiency
    • Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    • Multiple acyl-CoA dehydrogenase deficiency
    • Long-chain fatty acid plasma membrane transporter deficiency