Mayer-Rokitansky-Kuster-Hauser syndrome
MONDO:0017771Spectrum 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).
Also known as: MRKH, MRKH syndrome, Mayer-Rokitansky-Küster-Hauser Syndrome, Mullerian aplasia/dysgenesis, Rokitansky Kuster Hauser syndrome, Rokitansky syndrome, Mayer-Rokitansky-Küster-Hauser syndrome
10 clinical trials for this condition and its sub-types.
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