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Up to: Sulfur metabolism disease · Disorder of peptide and amine metabolism · Inborn disorder of the gamma-glutamyl cycle

Inherited glutathione metabolism disease

An inherited metabolic disease that is has its basis in the disruption of glutathione metabolic process.

0 trials tagged with this condition →

  • Inherited glutathione synthetase deficiency 1 trial Sub-types →
  • 5-oxoprolinase deficiency 0 trials
  • Gamma-glutamyl transpeptidase deficiency 0 trials
  • Gamma-glutamylcysteine synthetase deficiency 0 trials
  • Hemolytic anemia due to glutathione reductase deficiency 0 trials
  • Spondylometaphyseal dysplasia, Sedaghatian type 0 trials

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