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Mayer-Rokitansky-Kuster-Hauser syndrome

rare

Spectrum of Mullerian duct anomalies characterized by congenital aplasia of the uterus and upper 2/3 of the vagina in otherwise phenotypically normal females. It can be classified as either MRKH syndrome type 1 (corresponding to isolated utero-vaginal aplasia) or MRKH syndrome type 2 (utero-vaginal aplasia associated with other malformations).

Identifiers
MONDO:0017771 Orphanet:3109
Part of
Partial bilateral aplasia of the mullerian ductsSyndromic disease
Also known as
Mayer-Rokitansky-Küster-Hauser Syndrome · MRKH · MRKH syndrome · Mullerian aplasia/dysgenesis · Rokitansky Kuster Hauser syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Mayer-Rokitansky-Kuster-Hauser syndrome type 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2

Rare disease

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