1.1.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 1

AOA

Aminoacid and organic acids related disorders

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