Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency	Salt-losing congenital adrenal hyperplasia
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Steroid 21-monooxygenase deficiency, salt wasting type (disorder)
	Steroid 21-monooxygenase deficiency, salt wasting type
	21-hydroxylase deficiency, salt wasting type Congenital adrenal hyperplasia, type 2
	21-hydroxylasedeficiëntie met zoutverlies
	zoutverliezende vorm van 21-hydroxylasedeficiëntie AGS type 2 CAH type 2 congenitale bijnierhyperplasie type 2 adrenogenitaal syndroom type 2

Id	71578002
Status	Defined

Associated morphology	Hyperplasia
Finding site	Adrenal cortex structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Due to

Deficiency of steroid 21-monooxygenase

ICD-10 complex map reference set

Target	E25.0
Rule	TRUE
Advice	ALWAYS E25.0
Correlation	SNOMED CT source code to target map code correlation not specified