1.4.a

Disorders of carnitine metabolism

  • Primary carnitine deficiency
  • Carnitine palmitoyltransferase 1A deficiency
  • Carnitine palmitoyltransferase 1C deficiency (Autosomal dominant spastic paraplegia type 73)
  • Carnitine palmitoyltransferase 2 deficiency
  • Carnitine-acylcarnitine translocase deficiency
  • Epsilon-N-trimethyllysine hydroxylase deficiency
  • Gamma-butyrobetaine hydroxylase deficiency
  • Carnitine acetyltransferase deficiency

Subnetworks

cfao 1

C-FAO

Carbohydrate, fatty acid oxidation and ketone bodies disorders

Hey, want to upgrade to pro plan?

18748

Upgrade Now

& get 25% off

Offer valid only for 24 hrs.

18749
Scroll to Top