Systemic primary carnitine deficiency (Q3358135)

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amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy
  • CTD, SPCD
  • systemic primary carnitine deficiency disease
  • carnitine transporter deficiency
  • carnitine uptake defect
  • deficiency of plasma-membrane carnitine transporter
  • primary carnitine deficiency
  • renal carnitine transport defect (disorder)
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Language Label Description Also known as
English
Systemic primary carnitine deficiency
amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy
  • CTD, SPCD
  • systemic primary carnitine deficiency disease
  • carnitine transporter deficiency
  • carnitine uptake defect
  • deficiency of plasma-membrane carnitine transporter
  • primary carnitine deficiency
  • renal carnitine transport defect (disorder)

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