1.1.e

Disorders of the metabolism of sulfur-containing amino acids and hydrogen sulfide

  • Methionine adenosyltransferase I/III deficiency (Mudd’s disease)
  • Methionine adenosyltransferase II deficiency
  • Methanethiol oxidase deficiency (Extraoral halitosis)
  • Glycine N-methyltransferase deficiency
  • S-adenosylhomocysteine hydrolase deficiency
  • Adenosine kinase deficiency
  • Methionine synthase deficiency (Homocystinuria-megaloblastic anemia, cblG type)
  • Cystathionine beta-synthase deficiency (Classical homocystinuria)
  • Cystathionine gamma-lyase deficiency(Cystathioninuria)
  • Mercaptopyruvate sulfurtransferase deficiency (Mercaptolactate-cysteine disulfiduria)
  • Mitochondrial sulfide:quinone oxidoreductase deficiency
  • Mitochondrial sulfur dioxygenase deficiency (Ethylmalonic encephalopathy)
  • Isolated sulfite oxidase deficiency (Sulfocysteinuria)

Subnetworks

AOA 1

AOA

Aminoacid and organic acids related disorders

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