Orphanet: Distal hereditary motor neuropathy type 5

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Distal hereditary motor neuropathy type 5


Classification level: Disorder
  • Synonym(s):
    • Distal HMN V
    • Distal hereditary motor neuropathy type V
    • Distal spinal muscular atrophy type 5
    • dHMN5
  • Prevalence: -
  • Inheritance: Autosomal dominant 
  • Age of onset: Adolescent, Childhood, Adult
  • ICD-10: G12.2
  • OMIM: 600794  614751
  • UMLS: C1833308
  • MeSH: -
  • GARD: -
  • MedDRA: -

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