5.1.k

Other disorders of vitamin metabolism

  • Alpha-tocopherol transfer protein deficiency (Ataxia with isolated vitamin E deficiency)
  • Gamma-glutamyl carboxylase deficiency (Combined deficiency of vitamin K-dependent coagulation factors type 1)
  • Vitamin K epoxide reductase deficiency (Combined deficiency of vitamin K-dependent coagulation factors type 2)
  • Microsomal epoxide hydrolase deficiency (Familial hypercholanemia)
  • Menaquinone-4 synthetase deficiency (Schnyder corneal dystrophy)
  • L-dehydroascorbate transporter deficiency (GLUT1 deficiency; arterial tortuosity syndrome)

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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