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Becker
Congénitale SAI
Dominante
Dystrophie myotonique
Isaacs
Myotonie chondrodystrophique
Médicamenteuse
Neuromyotonie
Paramyotonie congénitale Pseudomyotonie
Récessive
Steinert
Symptomatique
Syndrome de Warburg-Thomsen
Thomsen

Translation of "Thomsen " (French → English) :

TERMINOLOGY
see also In-Context Translations below
syndrome de Warburg-Thomsen
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An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as
SNOMEDCT-BE (disorder) / 721084001
SNOMEDCT-BE (disorder) / 721084001
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https://browser.ihtsdotools.or (...) [HTML]
Dystrophie myotonique [Steinert] Myotonie:chondrodystrophique | congénitale:SAI | dominante [Thomsen] | récessive [Becker] | médicamenteuse | symptomatique | Neuromyotonie [Isaacs] Paramyotonie congénitale Pseudomyotonie
https://icd.who.int/browse10/2 (...) (...) [HTML]
Dystrophia myotonica [Steinert] Myotonia:chondrodystrophic | drug-induced | symptomatic | Myotonia congenita:NOS | dominant [Thomsen] | recessive [Becker] | Neuromyotonia [Isaacs] Paramyotonia congenita Pseudomyotonia
WORLD HEALTH ORGANIZATION ICD-10: G71.1
WORLD HEALTH ORGANIZATION ICD-10: G71.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
IN-CONTEXT TRANSLATIONS


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Thomsen

Date index:2023-07-29 -

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