OnlineIMD

Homocystinuria

  • Type
    Phenotype
  • Pathway
    • Metabolism of sulfur-containing amino acids and hydrogen sulfide
  • Associated genes
    Gene list
    • CBS Homocystinuria, classical
    • MTR Methionine synthase deficiency
    • MTRR Methionine synthase reductase deficiency
    • MTHFR 5,10-methylenetetrahydrofolate reductase deficiency
    • MTHFD1 Methylenetetrahydrofolate dehydrogenase 1 deficiency
    • MMCHC
    • MMACHC Methylmalonic aciduria and homocystinuria, cblC type
    • PRDX1 CcblC epimutation variant
    • HCFC1 Methylmalonic aciduria and homocystinuria, cblX type
    • THAP11 Ronin deficiency
    • ZNF143 ZNF143 deficiency
    • LMBD1
    • ABCD4 Methylmalonic aciduria and homocystinuria, cblJ type
    • MMADHC Methylmalonic aciduria and homocystinuria, cblD type
  • Disease group(s)
    • 1.5        Disorders of the metabolism of sulfur-containing amino acids