rokitansky sequence - CISMeF

CISMeF

chu

Rokitansky sequenceSNOMED Notion

Preferred Label : rokitansky sequence;

Details

Origin ID

D4-01549;

UMLS CUI

C0431648;

Currated CISMeF NLP mapping
- Mayer-Rokitansky-Kuster-Hauser Syndrome [NCIt concept]
- Mayer-Rokitansky-Kuster-Hauser syndrome [MedDRA Preferred Term]
- Mayer-Rokitansky-Küster-Hauser syndrome [ORDO Disease]
- Mayer-Rokitansky-Küster-Hauser syndrome type 1 [ORDO Disease]
- Mayer-rokitansky-kuster-hauser syndrome [OMIM Phenotype]
- Mullerian agenesis [ICD-11 More detail]
- Rokitansky Kuster Hauser syndrome [MeSH concept]
- Rokitansky sequence [MeSH concept]
- Rokitansky sequence (disorder) [SNOMED CT concept]
- Rokitansky-Kuster-Hauser syndrome [PASCAL descriptor]
- mullerian aplasia [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Other specified congenital malformations of female genitalia [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic urogenital tract malformation [ORDO Disease]
- Partial bilateral aplasia of the Müllerian ducts [ORDO Disease]
- Syndromic renal or urinary tract malformation [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Rokitansky sequence (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Mayer-Rokitansky-Küster-Hauser syndrome type 1 [ORDO Disease]
- Rokitansky sequence [MeSH concept]
- Rokitansky sequence (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
01/06/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.