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Amyotrophie spinale
Distale
Dystrophie endothéliale congénitale héréditaire type II
Déjerine-Sottas
Fazio-Londe
Forme scapulo-péronière
Hypertrophique de l'enfant
Kugelberg-Welander
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type 7
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivomotrice héréditaire type 4
Paralysie bulbaire progressive de l'enfant
Syndrome de Roussy-Lévy

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

neuropathie motrice distale héréditaire type Jerash
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 7
https://browser.ihtsdotools.or (...) (...) [HTML]
Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire de l'adulte jeune
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]
https://icd.who.int/browse10/2 (...) (...) [HTML]
Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form
WORLD HEALTH ORGANIZATION ICD-10: G12.1
WORLD HEALTH ORGANIZATION ICD-10: G12.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
dystrophie endothéliale congénitale héréditaire type II
https://browser.ihtsdotools.or (...) (...) [HTML]
Congenital hereditary endothelial dystrophy, 2
SNOMEDCT-BE (disorder) / 417395001
SNOMEDCT-BE (disorder) / 417395001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivomotrice héréditaire type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
Refsum's disease
SNOMEDCT-BE (disorder) / 25362006
SNOMEDCT-BE (disorder) / 25362006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1B
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : amyotrophie spinale adulte    déjerine-sottas    fazio-londe    kugelberg-welander    paralysie bulbaire progressive de l'enfant    syndrome de roussy-lévy    distale    enfant type ii    forme juvénile type iii    forme scapulo-péronière    hypertrophique de l'enfant    neuropathie sensitivomotrice héréditaire type    distale héréditaire type    


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distale héréditaire type

Date index:2022-11-18 -

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