Autosomal recessive hereditary disorder	Enzymopathy	Hyperammonemia	Inborn error of metabolism
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Hyperammonemia, type III (disorder)
	Hyperammonemia, type III
	Amino acid acetyltransferase deficiency AGA deficiency N-acetylglutamate transferase deficiency N-Acetylglutamate synthase deficiency N-acetylglutamate synthetase deficiency NAGS deficiency NAGS - N-Acetylglutamate synthase deficiency Congenital AGA deficiency
	hyperammoniëmie type III
	hyperammoniëmie door NAGS-deficiëntie hyperammoniëmie door N-acetylglutamatesynthasedeficiëntie

Id	57119000
Status	Primitive

Occurrence

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E72.2
Rule	TRUE
Advice	ALWAYS E72.2
Correlation	SNOMED CT source code to target map code correlation not specified