Orphanet: Autosomal dominant spastic paraplegia type 13
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Autosomal dominant spastic paraplegia type 13

Disease definition

A rare hereditary spastic paraplegia characterized by progressive spastic paraplegia with pyramidal signs in the lower limbs, decreased vibration sense, and increased reflexes in the upper limbs.

ORPHA:100994

Classification level: Disorder
  • Synonym(s):
    • SPG13
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adolescent, Adult
  • ICD-10: G11.4
  • OMIM: 605280
  • UMLS: C1854467
  • MeSH: C537485
  • GARD: 9616
  • MedDRA: -

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