Carnitine palmitoyltransferase II deficiency

（重定向自Carnitine palmityl transferase）

Carnitine palmitoyltransferase II deficiency has an autosomal recessive pattern of inheritance.

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.

单词	Carnitine palmityl transferase
释义	Carnitine palmityl transferase 英语百科 Carnitine palmitoyltransferase II deficiency （重定向自Carnitine palmityl transferase） 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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