disease has feature Klippel-Feil syndrome Mayer-Rokitansky-Küster-Hauser syndrome type 2 https://www.malacards.org/card/mullerian_duct_aplasia_unilateral_renal_agenesis_and_cervicothoracic_somite_anomalies Orphanet:2578 Mayer-Rokitansky-Küster-Hauser syndrome type 2 icd11.foundation:1521808255 DOID:0112179 GARD:0005513 SCTID:717705004 MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies UMLS:C4305568 OMIM:601076 MURCS Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome 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. atypical MRKH syndrome MONDO:0010989 MRKH syndrome type 2 MEDGEN:931237 MURCS association Mayer-Rokitansky-Kuster-Hauser syndrome