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

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

myotonia congenita [ Thomsen's disease | congenital myotonia ]

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


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


Myotonia congenita - autosomal dominant form

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


congenital myotonia | hereditary myotonia | Thomsen disease

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


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

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


ablatio falciformis congenita retinae 2.ablatio falciformis congenita | congenital retinal septum

décollement falciforme congénital de la rétine
IATE - Health
IATE - Health




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'Myotonia congenita NOS'

Date index:2024-05-24 -

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