1.01.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
Aminoacid and organic acids related disorders
