Mayer-Rokitansky-Kuster-Hauser syndrome

MONDO:0017771

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).

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.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by