FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Mayer-Rokitansky-Kuster-Hauser syndrome type 2 ID (Ontology) DOID:0112179 (Human Disease)
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.
Also Known As "atypical MRKH syndrome" ; "MRKH syndrome type 2" ; "mullerian duct aplasia, unilateral renal aplasia, and cervicothoracic somite dysplasia" (for all, see Synonyms field below)
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  syndrome
   |__Mayer-Rokitansky-Kuster-Hauser syndrome
       |__Mayer-Rokitansky-Kuster-Hauser syndrome type 2
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Synonyms
  • "atypical MRKH syndrome" EXACT
    "MRKH syndrome type 2" EXACT
    "mullerian duct aplasia, unilateral renal aplasia, and cervicothoracic somite dysplasia" EXACT
    "mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome" EXACT
    "MURCS" EXACT OMO:0003012
    "MURCS association" EXACT
Secondary IDs
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MIM:601076
ORDO:2578