5B5A.1

ICD-11 MMS 2026-01

Wernicke-Korsakoff Syndrome

Description

A thiamine-deficiency syndrome characterised by symmetric hyperaemic lesions of the brainstem, hypothalamus, thalamus, and mammillary bodies with glial proliferation, capillary dilatation, and perivascular haemorrhage. The syndrome is manifested by a confusional state, disorientation, ophthalmoplegia, nystagmus, diplopia, and ataxia (Wernicke encephalopathy), with severe loss of memory for recent events and confabulation (the invention of accounts of events to cover the loss of memory) (Korsakov psychosis) occurring following recovery. Defective binding of thiamine diphosphate by transketolase has been found. It appears that the disorder is of autosomal recessive inheritance but is expressed as clinical disease only in the event of thiamine deficiency.

Coding note

Chronic alcohol use may be associated with thiamine deficiency, but alcohol may also have effects on the brain via other mechanisms. This category should be used to describe cognitive symptoms due to chronic alcohol use if there is evidence of thiamine deficiency.

Excludes

  • 6D72.10 – Amnestic disorder due to use of alcohol

Exclusions from above levels

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  • NF07.0 – starvation
  • 18 – Pregnancy, childbirth or the puerperium
  • http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn

Child codes

  • 5B5A.10 – Wernicke encephalopathy
  • 5B5A.11 – Korsakoff syndrome
  • 5B5A.1Y – Other specified Wernicke-Korsakoff Syndrome
  • 5B5A.1Z – Wernicke-Korsakoff Syndrome, unspecified

Sibling codes

  • 5B5A.0 – Beriberi
  • 5B5A.Y – Other specified vitamin B1 deficiency
  • 5B5A.Z – Vitamin B1 deficiency, unspecified

Foundation entity

Wernicke-Korsakoff Syndrome – http://id.who.int/icd/entity/2017611840

Part of: 5B5A: Vitamin B1 deficiency › 05: Endocrine, nutritional or metabolic diseases