8E02.0

ICD-11 MMS 2026-01

Genetic Creutzfeldt-Jakob disease

Description

A disease of the brain, that is associated with a prion. This disease is characterised by neurological deficits, and is fatal. Confirmation is by pathological examination of the brain.

Index terms

  • Genetic Creutzfeldt-Jakob disease
  • CJD - [Creutzfeldt-Jakob disease]
  • Creutzfeldt-Jakob
Show allHide
  • Creutzfeldt-Jakob disease
  • JCD - [Jakob-Creutzfeldt disease]
  • Genetic prion disease due to prion gene mutations
  • Dementia due to Creutzfeldt-Jakob disease
  • transmissible virus dementia
  • Creutzfeldt-Jakob disease encephalopathy
  • Subacute spongiform encephalopathy

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
Show allHide
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • 8E02.1 – Gerstmann-Straussler-Scheinker syndrome
  • 8E02.2 – Fatal familial insomnia
  • 8E02.Y – Other specified genetic prion diseases
  • 8E02.Z – Genetic prion diseases, unspecified

Foundation entity

Genetic Creutzfeldt-Jakob disease – http://id.who.int/icd/entity/607607042

Allowed postcoordination axes

Part of: 8E02: Genetic prion diseases › 08: Diseases of the nervous system