- TypeGroup
- Disease group(s)
- Child entries
- Ornithine aminotransferase deficiency
- De Barsy syndrome
- ALDH18A1-related disease
- Pyrroline-5-carboxylate reductase 1 deficiency
- Pyrroline-5-carboxylate reductase 2 deficiency
- Hyperprolinemia
- Proline dehydrogenase deficiency
- Pyrroline-5-carboxylate dehydrogenase deficiency
- Hydroxyprolinemia
- Primary hyperoxaluria type 3