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Disease Charcot-Marie-Tooth
Déjerine-Sottas

Translation of "charcot-marie-tooth disease pyramidal features syndrome " (English → French) :

Charcot-Marie-Tooth disease, pyramidal features syndrome

neuropathie sensitivo-motrice héréditaire type 5
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004


Axonal Charcot-Marie-Tooth disease with pyramidal involvement

maladie de Charcot-Marie-Tooth type 2H
SNOMEDCT-BE (disorder) / 720637005
SNOMEDCT-BE (disorder) / 720637005


An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c

maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type B
SNOMEDCT-BE (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c / 773330000
SNOMEDCT-BE (disorder) / 773330000


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

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
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0




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'charcot-marie-tooth disease pyramidal features syndrome'

Date index:2022-01-27 -

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