Autosomal recessive hereditary disorder	Disorder of the gamma-glutamyl cycle	Enzymopathy	Inborn error of metabolism
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Glutathione synthase deficiency with 5-oxoprolinuria (disorder)
	Glutathione synthase deficiency with 5-oxoprolinuria
	Pyroglutamic aciduria 5-Oxoprolinuria Pyroglutamic acidemia
	glutathionsynthasedeficiëntie met 5-oxoprolinurie
	deficiëntie van glutathionsynthase met 5-oxoprolinurie

Id	39112005
Status	Primitive

Occurrence

Congenital

ICD-10 complex map reference set

Target	E72.8
Rule	TRUE
Advice	ALWAYS E72.8
Correlation	SNOMED CT source code to target map code correlation not specified