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Atrophic myotonia
Batten's disease
Batten-Steinert syndrome
Becker
Congenital myotonia
Curschmann-Batten-Steinert syndrome
Curschmann-Steinert syndrome
Dominant
Drug-induced
Dystrophia myotonica
Hereditary myotonia
Isaacs
Myotonia
Myotonia chondrodystrophic
Myotonia chondrodystrophica
Myotonia congenita
Myotonia congenita - autosomal dominant form
Myotonia congenita NOS
Myotonia fluctuans
Myotonia permanens
Myotonic dystrophy
Neuromyotonia
Osteochondromuscular dystrophy
Paramyotonia congenita Pseudomyotonia
Recessive
Schwartz-Jampel- Aberfeld syndrome
Steinert
Steinert's disease
Symptomatic
Thomsen
Thomsen disease
Thomsen's disease

Translation of "myotonia " (English → French) :

myotonia congenita [ Thomsen's disease | congenital myotonia ]

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


médecine > physiopathologie
médecine > physiopathologie


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


Myotonia chondrodystrophica | osteochondromuscular dystrophy | Schwartz-Jampel- Aberfeld syndrome

dystrophie ostéochondromusculaire | myopathie myotonique | myotonie chondrodystrophique | syndrome d’Aberfeld | syndrome Schwartz-Jampel
IATE - Health
IATE - Health


Myotonia congenita - autosomal dominant form

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


Myotonia fluctuans

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


Myotonia permanens

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


congenital myotonia | hereditary myotonia | Thomsen disease

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


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


myotonic dystrophy | Steinert's disease | Batten's disease | Batten-Steinert syndrome | Curschmann-Batten-Steinert syndrome | Curschmann-Steinert syndrome | atrophic myotonia

dystrophie myotonique | maladie de Steinert | myotonie dystrophique | myotonie de Steinert | dystrophie myotonique de Steinert | myopathie atrophique avec myotonie | atrophie myotonique | myopathie myotonique | myotonie atrophique | syndrome de Batten Steinert | syndrome de Curschmann-Batten-Steinert
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique




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'myotonia'

Date index:2021-05-13 -

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