3.2.b

Disorders of heme degradation and bilirubin metabolism

  • Heme oxygenase 1 deficiency
  • NADH-cytochrome b5 reductase deficiency (NADH diaphorase deficiency; methemoglobinemia types 1 and 2)
  • Cytochrome b5 deficiency (Methemoglobinemia type 4)
  • Biliverdin reductase alpha deficiency (Hyperbiliverdinemia)
  • UDP-glucuronosyltransferase A1 deficiency (Crigler-Najjar syndrome, severe; Gilbert syndrome, milder)
  • Canalicular bilirubin glucuronide transporter deficiency (Dubin-Johnson syndrome)
  • Rotor syndrome

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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