1.01.h
Disorders of lysine, hydroxylysine, and tryptophan metabolism
- Alpha-aminoadipic semialdehyde synthase deficiency (Familial hyperlysinemia; saccharopinuria)
- DHTKD1 deficiency (2-aminoadipic 2-oxoadipic aciduria; Charcot-Marie-Tooth disease type 2Q)
- 5-phosphohydroxylysine phospholyase deficiency (Phosphohydroxylysinuria)
- Hydroxylysinuria
- Tryptophan 2,3-dioxygenase deficiency (Hypertryptophanemia)
- Kynureninase deficiency (Xanthurenic aciduria; hydroxykynureninuria; vertebral, cardiac, renal, and limb defects syndrome type 2)
- 3-hydroxyanthranilic acid 3,4-dioxygenase deficiency (Vertebral, cardiac, renal, and limb \ defects \syndrome type 1)
- Kynurenine-3-hydroxylase deficiency
Subnetworks
AOA
Aminoacid and organic acids related disorders
