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MeSH term:
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Accepted terms:
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- Atrophy, Muscular, Peroneal
- HMSN Type I
- HMSN Type II
- Hereditary Motor and Sensory-Neuropathy Type II
- Hereditary Motor, and Sensory Neuropathy Type I
- Muscular Atrophy, Peroneal
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- Amyotrophie péronière
- Atrophie musculaire péronière
- Amyotrophie de Charcot-Marie-Tooth
- Maladie de Charcot-Marie
- Syndrome de Roussy-Lévy
- Dystasie aréflexique héréditaire
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- Charcot-Marie-Krankheit
- Peroneale Muskelatrophie
- Atrophie, muskuläre, peroneale
- Muskuläre Atrophie, peroneale
- Roussy-Lévy-Syndrom
- Neuropathie, Typ II, erbliche motorische und sensorische
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- Atrofia Fibular
- Atrofia Muscular Fibular
- SÃndrome de Roussy-Levy
- Sindrome de Roussy-Levy
- HMSN Tipo II
- NeuropatÃa Motora y Sensorial Hereditaria Tipo II
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- Neuropatia Motora e Sensitiva Hereditária Tipo I
- Neuropatia Motora e Sensitiva Hereditária Tipo II
- Atrofia Muscular Fibular
- SÃndrome de Roussy-Levy
- Neuropatia Motora e Sensorial Hereditaria Tipo II
- HMSN Tipo II
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