- TypeGroup
- Child entries
- Primary carnitine deficiency
- Carnitine palmitoyltransferase 1A 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