OnlineIMD

1.5        Disorders of the metabolism of sulfur-containing amino acids

  • Type
    Group
  • Pathway
    • Metabolism of sulfur-containing amino acids and hydrogen sulfide
  • Disease group(s)
    • 1        Disorders of amino acid metabolism
  • Child entries
    • Mercaptopyruvate sulfurtransferase deficiency
    • Methionine adenosyltransferase I/III deficiency
    • Methionine adenosyltransferase II deficiency
    • Glycine N-methyltransferase deficiency
    • S-Adenosylhomocysteine hydrolase deficiency
    • Methionine synthase deficiency
    • Homocystinuria
    • Homocystinuria, classical
    • Cystathioninuria
    • Immunodeficiency, developmental delay, and hypohomocysteinemia disease
    • Adenosine kinase deficiency
    • 21.10 Disorders of molybdenum cofactor metabolism
    • Taurine transporter deficiency