Autosomal recessive hereditary disorder	Disorder of sulfur-bearing amino acid metabolism	Enzymopathy	Inherited disorder of folate metabolism
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Glutamate formiminotransferase deficiency (disorder)
	Glutamate formiminotransferase deficiency
	FIGLUria Deficiency of glutamate formyltransferase Formiminoglutamic aciduria Deficiency of glutamate formiminotransferase
	deficiëntie van glutamaat-formiminotransferase
	glutamaat-formiminotransferasedeficiëntie

Id	59761008
Status	Primitive

Occurrence

DHD Diagnosis thesaurus reference set

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