carnitine palmitoyltransferase II deficiency (Q2033861)

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A lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria.
  • carnitine palmitoyltransferase II deficiency
  • CPT-II
  • infantile carnitine palmitoyltransferase II deficiency
  • late-onset carnitine palmitoyltransferase II deficiency
  • lethal neonatal carnitine palmitoyltransferase II deficiency
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Language Label Description Also known as
English
carnitine palmitoyltransferase II deficiency
A lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria.
  • carnitine palmitoyltransferase II deficiency
  • CPT-II
  • infantile carnitine palmitoyltransferase II deficiency
  • late-onset carnitine palmitoyltransferase II deficiency
  • lethal neonatal carnitine palmitoyltransferase II deficiency

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