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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant


Other Names for this Disease
  • CMT with pyramidal features
  • Hereditary motor and sensory neuropathy 5
  • HMSN 5
  • Peroneal muscular atrophy with pyramidal features, autosomal dominant
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