Inherited glutathione metabolism disease
MONDO:0040566An 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.
Follow this condition — get notified about new trialsSub-types
Glutathione synthetase deficiency with 5-oxoprolinuria
(1)
Inherited glutathione synthetase deficiency
(1)
5-oxoprolinase deficiency
(0)
Gamma-glutamylcysteine synthetase deficiency
(0)
Gamma-glutamyl transpeptidase deficiency
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Hemolytic anemia due to glutathione reductase deficiency
(0)
Spondylometaphyseal dysplasia, Sedaghatian type
(0)
Broader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Mineral metabolism disease
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of peptide and amine metabolism
(0)