Mayer-Rokitansky-Kuster-Hauser syndrome type 1

Rare Disease

MONDO:0010173

Also Known As

MRKH syndrome type 1Rokitansky sequencecongenital absence of uterus and vaginaMRKH anomalyMRKH syndromeMayer-Rokitansky-KUSTER-Hauser syndromeMayer-Rokitansky-Kuster-Hauser syndrome (MRKH)Mayer-Rokitansky-Küster-Hauser syndrome type 1Mrk anomalyMullerian aplasia/dysgenesisMullerian dysgenesisMüllerian agenesisRokitansky syndromeVon Mayer-Rokitansky-Kuster anomalycongenital absence of the uterus and vagina (CAUV)genital renal ear syndromeurogenital adysplasiauterus Bipartitus solidus Rudimentarius cum vagina Solida

Definition

Mayer-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.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

External Resources

Related Diseases

Mayer-Rokitansky-Küster-Hauser syndrome type 2

MONDO:0010989

Rare

← Back to All Diseases

Mayer-Rokitansky-Kuster-Hauser syndrome type 1

Also Known As

Definition

Patient-Friendly Information

External Resources

OMIM

Orphanet

GARD

Related Diseases