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Summary Literature (0)
DOID:0112179 - Mayer-Rokitansky-Kuster-Hauser syndrome type 2


Disease Ontology Definition:A Mayer-Rokitansky-Kuster-Hauser syndrome characterized by congenital aplasia of the uterus and upper two thirds of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects.

Synonyms: atypical MRKH syndrome, MRKH syndrome type 2, mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome, mullerian duct aplasia, unilateral renal aplasia, and cervicothoracic somite dysplasia, MURCS, MURCS association

Xenbase Genes :



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Mayer-Rokitansky-Kuster-Hauser syndrome (is_a)