Mayer-Rokitansky-Kuster-Hauser Syndrome Type 2
Disease ID: disease_node_20234
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| Dbxref | MIM:601076, ORDO:2578 |
|---|---|
| Subclassof | DOID_0112177 |
| Data Source | DOID |
| 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 |
| Doid Label | Mayer-Rokitansky-Kuster-Hauser syndrome type 2 |
| Doid Description | 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. |
| Disease Node Id | disease_node_20234 |
| Doid Id | DOID_0112179 |
| Label | Mayer-Rokitansky-Kuster-Hauser Syndrome Type 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Mayer-Rokitansky-Kuster-Hauser Syndrome(ID:disease_node_20233) (Disease)