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Déjerine-Sottas
Hypertrophique de l'enfant
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type 7
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie sensitivo-motrice héréditaire type Okinawa
Syndrome de Roussy-Lévy

Translation of "neuropathie motrice distale héréditaire type Jerash " (French → English) :

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 7

Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007


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 de l'adulte jeune

Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006


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 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




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neuropathie motrice distale héréditaire type Jerash

Date index:2022-05-28 -

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