Gargoylisme, Hunter-syndroom

Voorkeurslabel : Gargoylisme, Hunter-syndroom;

Wikipedia automatic translation : Syndroom van Hunter;

Wikipedia link : https://nl.wikipedia.org/wiki/Syndroom van Hunter;

Details

Oorsprong id

D016532;

UMLS CUI

C0026705;

False automatic mappings
- mucopolysacharidose I [MedDRA Preferred Term]
- mucopolysacharidose III [MedDRA Preferred Term]
Manual BTNT mappings - CISMeF
- Mucopolysacharidose type 2, geattenueerde vorm [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Lysosomale stapelingsziekte met skeletale betrokkenheid [ORDO Disease]
- Lysosomale ziekte met hypertrofische cardiomyopathie [ORDO Disease]
- Mucopolysacharidose met betrokkenheid van huid [ORDO Disease]
- Neurometabole ziekte [ORDO Disease]
- Syndromale neurometabole ziekte met X-gebonden intellectuele achterstand [ORDO Disease]
ORDO relation(s)
- Mucopolysacharidose type 2 [ORDO Disease]
UMLS correspondences (same concept)
- Hunter-syndroom [MedDRA LLT]
- Mucopolysaccharidose, type II [ICD-10 Sub-category (who)]
- Mucopolysacharidose type 2 [ORDO Disease]
- mucopolysacharidose II [MedDRA Preferred Term]
Validated automatic mappings to NTBT
- Mucopolysacharidose [ORDO Disease]
- mucopolysacharidose [MedDRA Preferred Term]

Keyword's position in hierarchy(ies) :

Main resources

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