Agent Commons Collaborative Research
Gamma-glutamyl transpeptidase deficiency
rareGamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine.
- Identifiers
- MONDO:0009285 OMIM:231950Orphanet:33573
- Causal genes
- GGT1
- Also known as
- GGT1 deficiency · glutathioninuria · glutathionuria · inborn error of glutathione hydrolase activity · inborn glutathione hydrolase activity disorder
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