Autosomal recessive hereditary disorder	Enzymopathy	Inborn error of metabolism	Non-ketotic hyperglycinemia
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Aminomethyltransferase deficiency (disorder)
	Aminomethyltransferase deficiency
	T-protein deficiency Non-ketotic hyperglycinemia type II Non-ketotic hyperglycinemia T protein deficiency Nonketotic hyperglycinemia, type II Tetrahydrofolate aminomethyltransferase deficiency T protein deficiency
	deficiëntie van aminomethyltransferase
	non-ketotische hyperglycinemie met deficiëntie van T-eiwit non-ketotische hyperglycinemie type 2 AMT-deficiëntie

Id	67845009
Status	Primitive

Occurrence

Congenital

ICD-10 complex map reference set

Target	E72.5
Rule	TRUE
Advice	ALWAYS E72.5
Correlation	SNOMED CT source code to target map code correlation not specified