Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

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maladie de Charcot-Marie-Tooth type 4B2

SNOMEDCT-BE (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso / 715800000

SNOMEDCT-BE (disorder) / 715800000

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Charcot-Marie-Tooth disease [ peroneal muscular atrophy ]

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maladie de Charcot-Marie-Tooth

Nervous System | Human Diseases - Various

Système nerveux | Maladies humaines diverses

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

IATE - Health

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

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maladie de Charcot-Marie-Tooth

IATE - Health

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Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.

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Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.

Organizations and Associations (Admin.) | International Bodies and Committees | Nervous System | Musculoskeletal System

Organismes et associations (Admin.) | Organismes et comités internationaux | Système nerveux | Appareil locomoteur (Médecine)

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peroneal muscular atrophy | Charcot Marie-Tooth disease

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

médecine

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

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

médecine

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Autosomal dominant Charcot-Marie-Tooth disease type 2K

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

SNOMEDCT-BE (disorder) / 719512003

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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

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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

WORLD HEALTH ORGANIZATION ICD-10: G60.0

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'Charcot-Marie-Tooth disease type 4D'

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