Dystrophia myotonica congenitalis

Voorkeurslabel : Dystrophia myotonica congenitalis;

Wikipedia automatic translation : Myotone dystrofie;

Wikipedia link : https://nl.wikipedia.org/wiki/Myotone dystrofie;

Details

Oorsprong id

D009223;

UMLS CUI

C0027126;

Manual NTBT mappings (CISMeF)
- Musculoskeletale ziekte met cataract [ORDO Disease]
- Myotonisch syndroom [ORDO Disease]
- Patroonvormige dystrofie van het retinale pigmentepitheel [ORDO Disease]
- Progressieve spierdystrofie [ORDO Disease]
Ne pas confondre avec
- Musculaire dystrofie [MeSH Descriptor]
ORDO relation(s)
- Myotone dystrofie [ORDO Disease]
See also
- DNA-repeat, expansie van [MeSH Descriptor]
- Expansion, trinucleotide-repeat- [MeSH Descriptor]
UMLS correspondences (same concept)
- Myotone dystrofie [ORDO Disease]
- dystrophia myotonica [MedDRA LLT]
- myotone dystrofie [MedDRA Preferred Term]
- ziekte van Steinert [MedDRA LLT]

Keyword's position in hierarchy(ies) :

Main resources

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