8B44.01

ICD-11 MMS 2026-01

Autosomal recessive hereditary spastic paraplegia

Index terms

  • Autosomal recessive hereditary spastic paraplegia
  • Autosomal recessive pure hereditary spastic paraplegia
  • Autosomal recessive pure hereditary spastic paraplegia due to mutations in Spatacsin gene
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  • Autosomal recessive spastic paraplegia type 24
  • Autosomal recessive spastic paraplegia type 28
  • Autosomal recessive spastic paraplegia type 30
  • Autosomal recessive spastic paraplegia type 5A
  • Autosomal recessive spastic paraplegia type 7
  • Autosomal recessive complex hereditary spastic paraplegia
  • Autosomal recessive complex hereditary spastic paraplegia due to mutations in Spatacsin gene
  • Autosomal recessive spastic paraplegia type 39
  • Autosomal recessive spastic paraplegia type 32
  • Autosomal recessive spastic paraplegia type 27
  • Autosomal recessive spastic paraplegia type 26
  • Autosomal recessive spastic paraplegia type 25
  • Autosomal recessive spastic paraplegia type 23
  • Autosomal recessive spastic paraplegia type 21
  • Autosomal recessive spastic paraplegia type 20
  • Autosomal recessive spastic paraplegia type 18
  • Autosomal recessive spastic paraplegia type 15
  • Autosomal recessive spastic paraplegia type 14
  • Autosomal recessive spastic paraplegia type 11

Exclusions from above levels

  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
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  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • 8B44.00 – Autosomal dominant hereditary spastic paraplegia
  • 8B44.02 – X-linked hereditary spastic paraplegia
  • 8B44.0Y – Other specified hereditary spastic paraplegia
  • 8B44.0Z – Hereditary spastic paraplegia, unspecified

Foundation entity

Autosomal recessive hereditary spastic paraplegia – http://id.who.int/icd/entity/1789135912

Part of: 8B44.0: Hereditary spastic paraplegia › 8B44: Degenerative myelopathic disorders › 08: Diseases of the nervous system