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Amyoplasia congenita
Arthrogryposis multiplex congenita
Becker
Congenital multiple arthrogryposis
Congenital myotonia
Dominant
Drug-induced
Dystrophia myotonica
Hereditary myotonia
Hypochondroplasia Osteosclerosis congenita
Isaacs
Myodystrophia fetalis
Myotonia
Myotonia chondrodystrophic
Myotonia congenita
Myotonia congenita - autosomal dominant form
Myotonia congenita NOS
Myotonia fluctuans
Myotonia permanens
Neuromyotonia
Paramyotonia congenita Pseudomyotonia
Recessive
Steinert
Symptomatic
Thomsen
Thomsen disease
Thomsen's disease

Translation of "Myotonia congenita " (English → French) :

myotonia congenita [ Thomsen's disease | congenital myotonia ]

maladie de Thomsen [ myotonie congénitale ]
Musculoskeletal System | Special Education
Appareil locomoteur (Médecine) | Éducation spéciale


Myotonia congenita - autosomal dominant form

myotonie congénitale, forme autosomique dominante
SNOMEDCT-BE (disorder) / 57938005
SNOMEDCT-BE (disorder) / 57938005


Dystrophia myotonica [Steinert] Myotonia:chondrodystrophic | drug-induced | symptomatic | Myotonia congenita:NOS | dominant [Thomsen] | recessive [Becker] | Neuromyotonia [Isaacs] Paramyotonia congenita Pseudomyotonia

Dystrophie myotonique [Steinert] Myotonie:chondrodystrophique | congénitale:SAI | dominante [Thomsen] | récessive [Becker] | médicamenteuse | symptomatique | Neuromyotonie [Isaacs] Paramyotonie congénitale Pseudomyotonie
WORLD HEALTH ORGANIZATION ICD-10: G71.1
WORLD HEALTH ORGANIZATION ICD-10: G71.1


congenital myotonia | hereditary myotonia | Thomsen disease

maladie de Thomsen | myotonic congénitale
IATE - Health
IATE - Health


arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]

arthrogrypose congénitale multiple [ amyoplasie congénitale | arthrogryposis multiplex congénitale | raideur articulaire congénitale | arthrogrypose | myodystrophie foetale ]
Bones and Joints | Musculoskeletal System | Symptoms (Medicine)
Os et articulations | Appareil locomoteur (Médecine) | Symptômes (Médecine)


Nervous System | Symptoms (Medicine)
Système nerveux | Symptômes (Médecine)


Myotonia fluctuans

myotonie fluctuante
SNOMEDCT-BE (disorder) / 715788001
SNOMEDCT-BE (disorder) / 715788001


Myotonia permanens

myotonie permanente
SNOMEDCT-BE (disorder) / 715789009
SNOMEDCT-BE (disorder) / 715789009


Arthrogryposis multiplex congenita

Arthrogrypose congénitale multiple
WORLD HEALTH ORGANIZATION ICD-10: Q74.3
WORLD HEALTH ORGANIZATION ICD-10: Q74.3


Hypochondroplasia Osteosclerosis congenita

Hypochondroplasie Ostéosclérose congénitale
WORLD HEALTH ORGANIZATION ICD-10: Q77.4
WORLD HEALTH ORGANIZATION ICD-10: Q77.4




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'Myotonia congenita'

Date index:2021-03-21 -

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