aangeboren defect van stofwisseling	congenitale adrenale hyperplasie	enzymopathie	hypoaldosteronisme	stoornis van metabolisme van steroïd
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deficiëntie van corticosteron-methyloxidase (aandoening)
	deficiëntie van corticosteron-methyloxidase
	corticosteron-methyloxidasedeficiëntie CMO-deficiëntie
	Corticosterone 18-monooxygenase deficiency
	Corticosterone methyl oxidase type II deficiency CMO II deficiency Corticosterone methyl oxidase type I deficiency CAH - 18-hydroxylase deficiency Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency 18-Hydroxycorticosterone dehydrogenase deficiency Aldosterone deficiency due to 18-hydroxylase defect 18-Hydroxylase deficiency CMO I deficiency

Id	47757001
Status	Primitive

Associated morphology	hyperplasie
Finding site	structuur van bijnierschors
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E27.4
Term	Overige en niet gespecificeerde bijnierschorsinsufficiëntie

SNOMED CT to ICD-10 extended map

Target	E27.4
Rule	TRUE
Advice	ALWAYS E27.4
Correlation	SNOMED CT source code to target map code correlation not specified