e/Carnitine-acylcarnitine translocase deficiency

Information
has gloss	eng: Carnitine-acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents long-chain fatty acids from being transported into the innermost part of the mitochondria for processing.
lexicalization	eng: Carnitine acylcarnitine translocase deficiency
lexicalization	eng: Carnitine-acylcarnitine translocase deficiency
lexicalization	eng: Carnitine/acylcarnitine Translocase Deficiency
instance of	(noun) an impairment of health or a condition of abnormal functioning disease

Media
media:img	Acyl-CoA from cytosol to the mitochondrial matrix.gif
media:img	Autorecessive.svg