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Mayer-Rokitansky-Küster-Hauser syndrome type 2
Disease Summary
Associated Targets ()
Mondo Description Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 2, a form of MRKH syndrome, is characterized by congenital aplasia of the uterus and upper 2/3 of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects. The acronym MURCS (MCllerian duct aplasia, Renal dysplasia, Cervical Somite anomalies) is also used.
Mondo Term and Equivalent IDs
MONDO:0010989: Mayer-Rokitansky-Küster-Hauser syndrome type 2
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0005513
OMIM:601076
Orphanet:2578
SCTID:717705004
MONDO:0010989
High level summary of knowledge for a disease, including descriptions and datasource references.