OnlineIMD

Methionine synthase deficiency

(cblG disease)
  • Synonym(s)
    • Homocystinuria-megaloblastic anemia, cblG type
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • MTR / 5-Methyltetrahydrofolate-Homocysteine Methyltransferase
      • 1q43
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • 5-methyltetrahydrofolate--homocysteine methyltransferase
  • Pathway
    • Metabolism of sulfur-containing amino acids and hydrogen sulfide
  • Disease group(s)
    • 1.5        Disorders of the metabolism of sulfur-containing amino acids