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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/601076
http://purl.bioontology.org/ontology/OMIM/601076
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|---|---|
| Preferred Name | MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACIC SOMITE ANOMALIES |
| Synonyms |
MRKH, TYPE II
MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME, TYPE II
KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA
MURCS
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MRKH, TYPE II
MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME, TYPE II
KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA
MURCS
|
|---|---|
| prefLabel | MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACIC SOMITE ANOMALIES
|
| Scope Statement | MURCS - MUllerian duct aplasia, Renal agenesis/ectopia, Cervical Somite dysplasia [MISCELLANEOUS]
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| type | |
| Has manifestation |
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| tui | T047
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| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
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| notation | 601076
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| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C4305568
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| Moved from | 148860
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| OMIM Entry Type | 5
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| OMIM MimType Value | perc
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| Delete | Subject | Author | Type | Created |
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| No notes to display |