Syndroom, Beckwith-Wiedemann-

Voorkeurslabel : Syndroom, Beckwith-Wiedemann-;

Wikipedia automatic translation : Syndroom van Beckwith-Wiedemann;

Wikipedia link : https://nl.wikipedia.org/wiki/Syndroom van Beckwith-Wiedemann;

Details

Oorsprong id

D001506;

UMLS CUI

C0004903;

Manual NTBT mappings (CISMeF)
- Genetische niertumor [ORDO Disease]
- Overgroeisyndroom [ORDO Disease]
- Paternale uniparentale disomie [ORDO Disease]
- Polymalformatief genetisch syndroom met verhoogd risico op het ontwikkelen van kanker [ORDO Disease]
- Syndromale renale of urinewegmalformatie [ORDO Disease]
- Syndroom geassocieerd met hypertrofische cardiomyopathie [ORDO Disease]
- Syndroom of malformatie geassocieerd met hoofd- en halsmalformaties [ORDO Disease]
- Zeldzame renale tumor [ORDO Disease]
ORDO relation(s)
- Syndroom van Beckwith-Wiedemann [ORDO Disease]
See also
- Genen, Wilms- [MeSH Descriptor]
- Gigantisme [MeSH Descriptor]
- Macroglossie [MeSH Descriptor]
- Omfalokèle [MeSH Descriptor]
Validated automatic mappings to NTBT
- Congenitale gestoorde-ontwikkelingssyndromen met vroege versterkte groei [ICD-10 Sub-category (who)]

Keyword's position in hierarchy(ies) :

Main resources

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