beckwith-wiedemann syndrome - CISMeF

CISMeF

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Beckwith-wiedemann syndromeSNOMED Notion

Preferred Label : beckwith-wiedemann syndrome;

Details

Origin ID

D4-00503;

UMLS CUI

C0004903;

Currated CISMeF NLP mapping
- Beckwith Wiedemann syndrome [Disease (Nov.)]
- Beckwith-Wiedemann Syndrome [NCIt concept]
- Beckwith-Wiedemann syndrome [PASCAL descriptor]
- Beckwith-Wiedemann syndrome [DO Concept]
- Beckwith-Wiedemann syndrome [ICD-11 More detail]
- Beckwith-Wiedemann syndrome [MeSH concept]
- Beckwith-Wiedemann syndrome [MedDRA Preferred Term]
- Beckwith-Wiedemann syndrome [ORDO Disease]
- Beckwith-Wiedemann syndrome (disorder) [SNOMED CT concept]
- Beckwith-wiedemann syndrome [OMIM Phenotype]
- beckwith-wiedemann syndrome [MeSH Descriptor]
ICD-10 exact mapping(s)
- Congenital malformation syndromes involving early overgrowth [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic renal tumor [ORDO Disease]
- Overgrowth syndrome [ORDO Disease]
- Paternal uniparental disomy [ORDO Disease]
- Polymalformative genetic syndrome with increased risk of developing cancer [ORDO Disease]
- Rare renal tumor [ORDO Disease]
- Syndrome associated with hypertrophic cardiomyopathy [ORDO Disease]
- Syndrome or malformation associated with head and neck malformations [ORDO Disease]
- Syndromic renal or urinary tract malformation [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Beckwith-Wiedemann syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Beckwith Wiedemann syndrome [Disease (Nov.)]
- Beckwith-Wiedemann Syndrome [NCIt concept]
- Beckwith-Wiedemann syndrome [ORDO Disease]
- Beckwith-Wiedemann syndrome [MedDRA Preferred Term]
- Beckwith-Wiedemann syndrome [MeSH concept]
- Beckwith-Wiedemann syndrome [DO Concept]
- Beckwith-Wiedemann syndrome [PASCAL descriptor]
- Beckwith-Wiedemann syndrome [ICD-11 More detail]
- Beckwith-Wiedemann syndrome (disorder) [SNOMED CT concept]
- Beckwith-wiedemann syndrome [OMIM Phenotype]
- beckwith-wiedemann syndrome [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

Main resources

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28/04/2025

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