OMOP Concept 36713399
Mayer-Rokitansky-Küster-Hauser syndrome type 2
StandardConditionSNOMED717705004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Mayer-Rokitansky-Küster-Hauser syndrome type 2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 717705004 | Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Non-standard |
Synonyms
Alternative names recorded for Mayer-Rokitansky-Küster-Hauser syndrome type 2 across source vocabularies.
- Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome
- Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)
- Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome
- síndrome de aplasia del conducto de Müller, displasia renal y anomalías de los somitas cervicales
- síndrome de aplasia mulleriana, displasia renal y anomalías de los somitas cervicales
- síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2
- síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2 (trastorno)
- síndrome MRKH (Mayer Rokitansky Kuster Hauser) atípico
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(51)Roll up to these when you need a wider cohort.
- 1Mayer Rokitansky Küster Hauser syndrome
- 2Congenital absence of uterus
- 2Congenital absence of vagina
- 2Genetic disease
- 2Malformation sequence
- 3Congenital anomaly of vagina
- 3Congenital malformation syndrome
- 3Congenital uterine anomaly
- 3Disease
- 3Uterus absent
- 3Vagina absent
- 4Clinical finding
- 4Congenital anomaly of abdomen
- 4Congenital anomaly of female genital system
- 4Congenital anomaly of the pelvis
- 4Congenital malformation
- 4Disorder of uterus
- 4Disorder of vagina
- 4Uterus finding
- 4Vagina finding
- 5Congenital anomaly of lower trunk
- 5Congenital disease
- 5Congenital female urogenital anomaly
- 5Congenital malformation of genital organs
- 5Developmental disorder
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