Inherited glutathione metabolism disease

MONDO:0040566

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

Also known as: disorder of glutathione metabolism, glutathione metabolism disorder, inherited, inborn error of glutathione metabolic process, inborn error of glutathione metabolism, inborn glutathione metabolic process disorder, rare inborn error of glutathione metabolic process

2 clinical trials for this condition and its sub-types, 0 tagged with Inherited glutathione metabolism disease itself.

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Where it sits in the disease tree

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Part of

↑ Sulfur metabolism disease (14) ↑ Disorder of peptide and amine metabolism (4) ↑ Inborn disorder of the gamma-glutamyl cycle (1)

Sub-types of Inherited glutathione metabolism disease

Inherited glutathione synthetase deficiency 1 trial
2 sub-types
- Glutathione synthetase deficiency with 5-oxoprolinuria 1 trial
- Glutathione synthetase deficiency without 5-oxoprolinuria 0 trials
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

Including sub-types (2) Tagged with Inherited glutathione metabolism disease (0)

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