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Mayer-Rokitansky-Kuster-Hauser syndrome type 1
rareMayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1, a form of MRKH syndrome, is an isolated form of congenital aplasia of the uterus and 2/3 of the vagina occurring in otherwise phenotypically normal females.
- Identifiers
- MONDO:0010173 OMIM:277000Orphanet:247775
- Also known as
- congenital absence of the uterus and vagina (CAUV) · congenital absence of uterus and vagina · genital renal ear syndrome · Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) · MRKH syndrome
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