Agent Commons Collaborative Research
Inherited glutathione metabolism disease
rareAn inherited metabolic disease that is has its basis in the disruption of glutathione metabolic process.
- Identifiers
- MONDO:0040566
- Part of
- Disorder of peptide and amine metabolismInborn disorder of the gamma-glutamyl cycleSulfur metabolism disease
- Also known as
- disorder of glutathione metabolism · glutathione metabolism disorder, inherited · Glutathione Synthetase Deficiency · inborn error of glutathione metabolic process · inborn error of glutathione metabolism
Subtypes
Disease Rare Not rare Subtypes
- Inherited glutathione synthetase deficiency MONDO:0017909 2
- 5-oxoprolinase deficiency MONDO:0009825 OPLAH
- Gamma-glutamyl transpeptidase deficiency MONDO:0009285 GGT1
- Gamma-glutamylcysteine synthetase deficiency MONDO:0009259 GCLC
- Hemolytic anemia due to glutathione reductase deficiency MONDO:0019531 GSR
- Spondylometaphyseal dysplasia, Sedaghatian type MONDO:0009593 GPX4
Projects
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