8B60.6ICD-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
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- Monomelic amyotrophy of lower limb
Exclusions from above levels
05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth and the puerperium19– 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 sclerosis8B60.1– Progressive bulbar palsy8B60.2– Progressive pseudobulbar palsy8B60.3– Progressive muscular atrophy8B60.4– Primary lateral sclerosis8B60.5– Amyotrophic lateral sclerosis-Plus8B60.7– Madras type motor neuron disease8B60.Y– Other specified motor neuron disease8B60.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