5.01.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
NOMS
Disorders of neuromodulators and other small molecules
