Glutathionuria

Glutathionuria

Glutathione
Classification and external resources
OMIM	231950

Glutathionuria is the presence of glutathione in the urine, and is a rare inborn error of metabolism.^[1]

The condition has been identified in five patients.^[2]

References

↑ Schulman JD, Goodman SI, Mace JW, Patrick AD, Tietze F, Butler EJ (July 1975). "Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase". Biochem. Biophys. Res. Commun. 65 (1): 68–74. doi:10.1016/S0006-291X(75)80062-3. PMID 238530.
↑ John Fernandes (2006). Inborn metabolic diseases: diagnosis and treatment. Springer. pp. 187–. ISBN 978-3-540-28783-4. Retrieved 1 May 2011.

Eicosanoid metabolism disorders

Prostanoids	PTGIS (Essential hypertension) TBSAX1 (Ghosal hematodiaphyseal dysplasia)

Leukotrienes	LTC4s (Leukotriene C4 synthase deficiency) GGT1 (Glutathionuria)

Other/ungrouped	HPGD (Primary hypertrophic osteoathropathy)

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