congenitale afwezigheid van uterus	congenitale afwezigheid van vagina	genetische aandoening	malformatiesequentie
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syndroom van Mayer-Rokitansky-Küster-Hauser (aandoening)
	syndroom van Mayer-Rokitansky-Küster-Hauser
	Mayer-Rokitansky-Küster-Hauser-syndroom MRKH-syndroom MRK-syndroom
	Mayer Rokitansky Küster Hauser syndrome
	Rokitansky syndrome MRKH syndrome
	A rare spectrum of Mullerian duct anomalies characterized by congenital aplasia of the uterus and upper two-thirds of the vagina in otherwise phenotypically normal females. It can be classified as either Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1 (corresponding to isolated utero-vaginal aplasia) or MRKH syndrome type 2 (utero-vaginal aplasia associated with other malformations).

Id	1354648006
Status	Primitive

Associated morphology	afwezigheid
Finding site	structuur van bovenste derde deel van vagina
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	afwezigheid
Finding site	structuur van uterus
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	afwezigheid
Finding site	structuur van middelste derde deel van vagina
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	Q51.8
Term	Overige gespecificeerde congenitale misvormingen van uterus en cervix

SNOMED CT to ICD-10 extended map

Target	Q51.8
Rule	TRUE
Advice	ALWAYS Q51.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

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Mayer-Rokitansky-Küster-Hauser-syndroom type 1

Mayer-Rokitansky-Küster-Hauser-syndroom type 2