- TypeGroup
- Disease group(s)
- Child entries
- Hyperlysinemia, familial
- Antiquitin deficiency
- 2-Aminoadipic 2-oxoadipic aciduria
- Hartnup disease
- DNAJC12 deficiency
- Glutaric aciduria type 1
- Phosphohydroxylysinuria
- Mitochondrial oxodicarboxylate carrier deficiency
- Hypertryptophanemia
- Kynureninase deficiency
- 3-hydroxyanthranilic acid 3,4-dioxygenase deficiency
- Kynurenine-3-hydroxylase deficiency