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Translation of "Neuropathie héréditaire motrice et sensorielle " (French → English) :
TERMINOLOGY
see also In-Context Translations below Neuropathie héréditaire motrice et sensorielle
Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
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
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
neuropathie sensitivo-motrice axonale héréditaire avec acrodystrophie
A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyeliti
SNOMEDCT-BE (disorder) / 771144005
SNOMEDCT-BE (disorder) / 771144005
neuropathie sensitivo-motrice héréditaire type 5
Charcot-Marie-Tooth disease, pyramidal features syndrome
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004
neuropathie sensitivo-motrice héréditaire type Okinawa
An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006
neuropathie motrice distale héréditaire de l'adulte jeune
Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
neuropathie motrice distale héréditaire type Jerash
Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
neuropathie motrice distale héréditaire type 1
Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
neuropathie motrice distale héréditaire type 7
Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007
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Neuropathie héréditaire motrice et sensorielle
Date index:2021-09-30 -
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