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Déjerine-Sottas
Hypertrophique de l'enfant
Maladie de Charcot-Marie-Tooth liée à l'X type 4
Maladie de Charcot-Marie-Tooth type 4
Syndrome de Roussy-Lévy

Translation of "charcot-marie-tooth type " (French → English) :

TERMINOLOGY
see also In-Context Translations below
Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
https://icd.who.int/browse10/2 (...) (...) [HTML]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2B
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2B
SNOMEDCT-BE (disorder) / 717008005
SNOMEDCT-BE (disorder) / 717008005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2N
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2N
SNOMEDCT-BE (disorder) / 719515001
SNOMEDCT-BE (disorder) / 719515001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2K
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2K
SNOMEDCT-BE (disorder) / 719512003
SNOMEDCT-BE (disorder) / 719512003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth liée à l'X type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)
SNOMEDCT-BE (disorder) / 763400005
SNOMEDCT-BE (in particular of the peroneal group) / 763400005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive demyelinating Charcot-Marie-Tooth
SNOMEDCT-BE (disorder) / 715795005
SNOMEDCT-BE (disorder) / 715795005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2L
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2L
SNOMEDCT-BE (disorder) / 719513008
SNOMEDCT-BE (disorder) / 719513008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2C
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2C
SNOMEDCT-BE (disorder) / 717010007
SNOMEDCT-BE (disorder) / 717010007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2E
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2E
SNOMEDCT-BE (disorder) / 717012004
SNOMEDCT-BE (disorder) / 717012004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2D
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2D
SNOMEDCT-BE (disorder) / 717011006
SNOMEDCT-BE (disorder) / 717011006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS


Others have searched : déjerine-sottas    syndrome de roussy-lévy    hypertrophique de l'enfant    maladie de charcot-marie-tooth type    charcot-marie-tooth type    


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charcot-marie-tooth type

Date index:2021-08-26 -

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