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Mutilating hereditary sensory neuropathy with spastic paraplegia

Disease definition

This syndrome is characterized by the association of an axonal sensory and autonomic neuropathy with spastic paraplegia.

ORPHA:139578

Classification level: Disorder
  • Synonym(s):
    • Mutilating HSAN with spastic paraplegia
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood, Infancy
  • ICD-10: G60.8
  • OMIM: 256840
  • UMLS: C1850395
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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