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Acropathie ulcéromutilante
Déjerine-Sottas
Hypertrophique de l'enfant
Maladie de Thévenard
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie radiculaire sensitive héréditaire
Récessive
Syndrome de Nélaton
Syndrome de Roussy-Lévy

Translation of "Neuropathie héréditaire sensitive et autonomique type 1 " (French → English) :

neuropathie héréditaire sensitive et autonomique type 1

Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008


neuropathie héréditaire sensitive et autonomique type 1B

Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008


neuropathie héréditaire sensitive et autonomique

Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005


acropathie ulcéromutilante | maladie de Thévenard | neuropathie radiculaire sensitive héréditaire

Denny Brown's syndrome
IATE - Health
IATE - Health


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


Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton

Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8




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Neuropathie héréditaire sensitive et autonomique type 1

Date index:2021-03-14 -

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