Orphanet: Distal hereditary motor neuropathy type 2
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Distal hereditary motor neuropathy type 2

ORPHA:139525

Classification level: Disorder
  • Synonym(s):
    • Distal spinal muscular atrophy type 2
    • dHMN2
    • dSMA2
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adolescent, Adult
  • ICD-10: G12.2
  • OMIM: 158590  608634  613376  615575
  • UMLS: C1854023  C3711384
  • MeSH: -
  • GARD: -
  • MedDRA: -

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An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

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