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inherited glutathione synthetase deficiency

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Glutathione synthetase deficiency is characterised by hemolytic anemia, associated with metabolic acidosis and 5-oxoprolinuria in moderate forms, and with progressive neurological symptoms and recurrent bacterial infections in the most severe forms.
Mondo Term and Equivalent IDs
MONDO:0017909:  inherited glutathione synthetase deficiency
GARD:0010047: 
MESH:C536835: 
NCIT:C128193: 
Orphanet:32: 
SCTID:234589002: 
UMLS:C0398746: