8B60.5

ICD-11 MMS 2026-01

Amyotrophic lateral sclerosis-Plus

Description

This category represents a group of disorders with motor symptoms of ALS and superimposed features of dysfunction of other neurological systems, such as extrapyramidal, cerebellar or cognitive dysfunction.

Index terms

  • Amyotrophic lateral sclerosis-Plus
  • Amyotrophic lateral sclerosis with autonomic dysfunction
  • Amyotrophic lateral sclerosis with multiple system atrophy
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  • Amyotrophic lateral sclerosis with spinocerebellar ataxia
  • Amyotrophic lateral sclerosis-parkinsonism-dementia complex of Guam
  • Parkinsons-Dementia Complex
  • Western Pacific Amyotrophic Lateral Sclerosis
  • Amyotrophic lateral sclerosis-parkinsonism-dementia complex of Kii Peninsula
  • Amyotrophic lateral sclerosis-parkinsonism-dementia complex of West New Guinea
  • Amyotrophic lateral sclerosis with frontotemporal dementia
  • Amyotrophic lateral sclerosis with parkinsonism
  • Amyotrophic lateral sclerosis with cerebellar dysfunction

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

  • 8B60.0 – Amyotrophic lateral sclerosis
  • 8B60.1 – Progressive bulbar palsy
  • 8B60.2 – Progressive pseudobulbar palsy
  • 8B60.3 – Progressive muscular atrophy
  • 8B60.4 – Primary lateral sclerosis
  • 8B60.6 – Monomelic amyotrophy
  • 8B60.7 – Madras type motor neuron disease
  • 8B60.Y – Other specified motor neuron disease
  • 8B60.Z – Motor neuron disease, unspecified

Foundation entity

Amyotrophic lateral sclerosis-Plus – http://id.who.int/icd/entity/620164044

Allowed postcoordination axes

Part of: 8B60: Motor neuron disease › 08: Diseases of the nervous system