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

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)