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Amyotrophie de Charcot-Marie-Tooth
Amyotrophie péronière
Amyotrophie péronière de Charcot-Marie-Tooth
Atrophie de Charcot-Marie
Atrophie péronière
CMT
Déjerine-Sottas
Hypertrophique de l'enfant
Maladie de Charcot-Marie
Maladie de Charcot-Marie-Tooth
Maladie de Charcot-Marie-Tooth liée à l'X type 4
Maladie de Charcot-Marie-Tooth type 4
Neuropathie héréditaire de Charcot-Marie-Tooth
Syndrome de Charcot-Marie
Syndrome de Charcot-Marie-Tooth-Hoffmann
Syndrome de Roussy-Lévy

Translation of "Maladie de Charcot-Marie-Tooth " (French → English) :

maladie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease [ peroneal muscular atrophy ]
Système nerveux | Maladies humaines diverses
Nervous System | Human Diseases - Various


maladie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | CMT [Abbr.]
IATE - Health
IATE - Health


maladie de Charcot-Marie-Tooth liée à l'X type 4

A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)
SNOMEDCT-BE (disorder) / 763400005
SNOMEDCT-BE (in particular of the peroneal group) / 763400005


maladie de Charcot-Marie-Tooth type 4

Autosomal recessive demyelinating Charcot-Marie-Tooth
SNOMEDCT-BE (disorder) / 715795005
SNOMEDCT-BE (disorder) / 715795005


maladie de Charcot-Marie-Tooth autosomique dominante type 2K

Autosomal dominant Charcot-Marie-Tooth disease type 2K
SNOMEDCT-BE (disorder) / 719512003
SNOMEDCT-BE (disorder) / 719512003


amyotrophie péronière de Charcot-Marie-Tooth | CMT | maladie de Charcot-Marie-Tooth | neuropathie héréditaire de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]
IATE - Health
IATE - Health


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


maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy
médecine
médecine


amyotrophie péronière | syndrome de Charcot-Marie-Tooth-Hoffmann

peroneal muscular atrophy | Charcot Marie-Tooth disease
médecine
médecine




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Maladie de Charcot-Marie-Tooth

Date index:2021-01-01 -

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