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Translation of "neuropathie héréditaire " (French → English) :
TERMINOLOGY
see also In-Context Translations below neuropathie héréditaire sensitive et autonomique
Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005
Neuropathie héréditaire et idiopathique
Hereditary and idiopathic neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60
WORLD HEALTH ORGANIZATION ICD-10: G60
neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement
This syndrome has characteristics of sensory and autonomic axonal neuropathy, sensorineural hearing loss and persistent global developmental delay. It has been described in four individuals from a consanguineous Lebanese family. Onset occurred in inf
SNOMEDCT-BE (disorder) / 717826009
SNOMEDCT-BE (disorder) / 717826009
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 type 1
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
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
Autres neuropathies héréditaires et idiopathiques
Other hereditary and idiopathic neuropathies
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8
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 de l'adulte jeune
Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
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neuropathie héréditaire
Date index:2022-09-05 -
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