aangeboren defect van stofwisseling	autosomaal recessieve hereditaire aandoening	enzymopathie	non-ketotische hyperglycinemie
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non-ketotische hyperglycinemie met deficiëntie van P-eiwit (aandoening)
	non-ketotische hyperglycinemie met deficiëntie van P-eiwit
	non-ketotische hyperglycinemie type 1
	Glycine dehydrogenase (decarboxylating) deficiency
	Non-ketotic hyperglycinemia type I P protein deficiency Glycine dehydrogenase decarboxylating deficiency Glycine decarboxylase deficiency Non-ketotic hyperglycinemia P protein deficiency P-protein deficiency Nonketotic hyperglycinemia, type I

Id	63329001
Status	Primitive

Occurrence

congenitaal

SNOMED CT to ICD-10 extended map

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