disease has feature Klippel-Feil syndrome Mayer-Rokitansky-Küster-Hauser syndrome type 2 GARD:0005513 ICD10:Q87.8 Klippel-Feil deformity, conductive deafness, and absent vagina MONDO:0010989 MRKH syndrome type 2 MRKH, type 2 MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies MURCS MURCS association Mayer-Rokitansky-Kuster-Hauser syndrome, type 2 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. Mayer-Rokitansky-Küster-Hauser syndrome type 2 Mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome OMIM:601076 Orphanet:2578 SCTID:717705004 atypical MRKH syndrome syndromic anorectal malformation Mayer-Rokitansky-Kuster-Hauser syndrome