Wermer-syndroom - CISMeF

CISMeF

chu

Wermer-syndroomDescripteur MeSH

Voorkeurslabel : Wermer-syndroom;

Details

Oorsprong id

D018761;

UMLS CUI

C0025267;

Currated CISMeF NLP mapping
- MEA type I [MedDRA LLT]
- MEN type I [MedDRA LLT]
- Multipele endocriene neoplasie type 1 [ORDO Disease]
- multipele endocriene adenomatose type I [MedDRA LLT]
- multipele endocriene neoplasie type 1 [MedDRA Preferred Term]
- multipele endocriene neoplasie type I [MedDRA LLT]
Manual NTBT mappings (CISMeF)
- ACTH-afhankelijk syndroom van Cushing [ORDO Disease]
- ACTH-onafhankelijk syndroom van Cushing [ORDO Disease]
- Familiale primaire hyperparathyreoïdie [ORDO Disease]
- Genetische hyperparathyreoïdie [ORDO Disease]
- Overgeërfd kankerpredispositiesyndroom [ORDO Disease]
- Zeldzame bijschildkliertumor [ORDO Disease]
- Zeldzame hyperparathyreoïdie [ORDO Disease]
ORDO relation(s)
- Multipele endocriene neoplasie type 1 [ORDO Disease]
See also
- Eilandceltumor, ulcerogene [MeSH Descriptor]
- Parathyroïdie, hyper- [MeSH Descriptor]
- Syndroom, Zollinger-Ellison- [MeSH Descriptor]
UMLS correspondences (same concept)
- MEA type I [MedDRA LLT]
- MEN type I [MedDRA LLT]
- Multipele endocriene neoplasie type 1 [ORDO Disease]
- multipele endocriene adenomatose type I [MedDRA LLT]
- multipele endocriene neoplasie type 1 [MedDRA Preferred Term]
- multipele endocriene neoplasie type I [MedDRA LLT]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
29/10/2025

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