Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyltransferase II deficiency (CPT-II) is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source.
CPT II deficiencyCarnitine Palmityl Transferase DeficiencyCarnitine palmitoyl transferase 2 deficiencyCarnitine palmitoyltransferase deficiency type IICarnitine palmitoyltransferase ii deficiencyCarnitine palmityl transferaseCarnitine palmityl transferase deficiency type 2Hereditary carnitine deficiency myopathyMuscle form of carnitine palmitoyltransferase deficiency
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Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyltransferase II deficiency (CPT-II) is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source.
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Carnitine palmitoyltransferase ...... rcise or periods without food.
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La deficiencia de la enzima ca ...... : la infantil y la del adulto.
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Le déficit en carnitine palmit ...... ement une mutation spécifique.
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740,196,045
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Carnitine palmitoyltransferase ...... ilization as an energy source.
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La deficiencia de la enzima ca ...... : la infantil y la del adulto.
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Le déficit en carnitine palmit ...... yoglobinurie lors des efforts.
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Carnitine palmitoyltransferase II deficiency
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Deficiencia de carnitina palmitoiltransferasa tipo II
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Déficit en carnitine palmitoyltransférase II
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Carnitine palmitoyltransferase II deficiency
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