Orphanet: Hereditary sensory and autonomic neuropathy type 2

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Hereditary sensory and autonomic neuropathy type 2

Disease definition

A rare hereditary sensory and autonomic neuropathy characterized by profound and universal sensory loss involving large and small fiber nerves.


Classification level: Disorder
  • Synonym(s):
    • Autosomal recessive sensory radicular neuropathy
    • HSAN2
    • Hereditary sensory and autonomic neuropathy type II
    • Neurogenic acroosteolysis
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: G60.8
  • OMIM: 201300  243000  613115  614213
  • UMLS: C0020072  C0270914
  • MeSH: -
  • GARD: 3976
  • MedDRA: -

Detailed information


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