inherited glutathione synthetase deficiency (MONDO_0017909, a Monarch Disease Ontology term) can be described as follows. Glutathione synthetase deficiency is characterized 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. Also known as: 5-oxoprolinuria, GSSD, glutathione synthetase deficiency, inborn error of glutathione synthase activity, inborn glutathione synthase activity disorder, pyroglutamic aciduria, pyroglutamicaciduria, rare inborn error of glutathione synthase activity.