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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
Dit betekent dat je vagina en baarmoeder niet of niet goed zijn gegroeid. Je bent met dit probleem geboren.
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).
Id1354648006
StatusPrimitive
Associated morphologyafwezigheid
Finding sitestructuur van uterus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map
DHD Diagnosis thesaurus reference set
SNOMED CT to ICD-10 extended map
TargetQ51.8
RuleTRUE
AdviceALWAYS Q51.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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