8B60.6

ICD-11 MMS 2026-01

Monomelic amyotrophy

Description

Atrophy and weakness restricted to one upper or lower limb, onset in the second or third decade, male predominance, and sporadic occurrence are characteristic features of MMA. Other typical features include: insidious onset of lower motor neuron signs due to anterior horn cell involvement, absence of upper motor neuron signs, slow progression followed by stabilization within a few years,, and a benign symptomatic disease course. MMA is particularly prevalent in Asia although it is encountered worldwide.

Index terms

  • Monomelic amyotrophy
  • Monomelic amyotrophy of upper limb
  • Hirayama disease
Show allHide
  • Monomelic amyotrophy of lower limb

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

  • 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
  • 8B60.5 – Amyotrophic lateral sclerosis-Plus
  • 8B60.7 – Madras type motor neuron disease
  • 8B60.Y – Other specified motor neuron disease
  • 8B60.Z – Motor neuron disease, unspecified

Foundation entity

Monomelic amyotrophy – http://id.who.int/icd/entity/2090347823

Allowed postcoordination axes

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