8B61.4

ICD-11 MMS 2026-01

Localised spinal muscular atrophy

Description

This category comprises a group of disorders with a varied pattern of weakness and autosomal dominant or X-linked recessive inheritance with specific genetic profiles.

Index terms

  • Localised spinal muscular atrophy
  • localised SMA - [spinal muscular atrophy]
  • Distal form of spinal muscular atrophy
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  • Distal HMN - [hereditary motor neuropathy]
  • Distal hereditary motor neuropathy
  • Distal hereditary motor neuropathy, autosomal dominant
  • Distal HMN - [hereditary motor neuropathy] autosomal dominant
  • Distal spinal muscular atrophy, autosomal dominant
  • Autosomal dominant benign distal spinal muscular atrophy
  • Autosomal dominant congenital benign spinal muscular atrophy
  • Distal hereditary motor neuropathy type 1
  • DHMN1 - [Distal hereditary motor neuropathy type 1]
  • Distal hereditary motor neuropathy type 2
  • DHMN2 - [Distal hereditary motor neuropathy type 2]
  • Distal hereditary motor neuropathy type 5
  • DHMN5 - [Distal hereditary motor neuropathy type 5]
  • Distal hereditary motor neuropathy type 7
  • DHMN7 - [Distal hereditary motor neuropathy type 7]
  • Distal hereditary motor neuropathy, autosomal recessive
  • Distal HMN - [hereditary motor neuropathy] autosomal recessive
  • Distal spinal muscular atrophy, autosomal recessive
  • Autosomal recessive lower motor neuron disease with childhood onset
  • Autosomal recessive distal spinal muscular atrophy type 4
  • dSMA4 - [Autosomal recessive distal spinal muscular atrophy type 4]
  • Distal hereditary motor neuropathy type 3 and type 4
  • dSMA3 and dSMA4 - [Distal hereditary motor neuropathy type 3 and type 4]
  • Distal hereditary motor neuropathy, Jerash type
  • Distal spinal muscular atrophy type 2
  • Spinal muscular atrophy with respiratory distress
  • Distal hereditary motor neuronopathy type 6
  • SMARD - [Spinal muscular atrophy with respiratory distress]
  • Severe infantile axonal neuropathy with respiratory failure
  • Distal hereditary motor neuropathy, X-linked
  • Distal HMN, X-linked
  • Distal spinal muscular atrophy, X-linked
  • Scapuloperoneal form of spinal muscular atrophy
  • SPSMA - [Scapuloperoneal form of spinal muscular atrophy]
  • Facioscapulohumeral form of spinal muscular atrophy
  • FSHSMA - [Facioscapulohumeral form of spinal muscular atrophy]
  • Facioscapulohumeral form of spinal muscular atrophy with sensory loss
  • Davidenkow Disease
  • Scapulohumeral form of spinal muscular atrophy
  • Oculopharyngeal form of spinal muscular atrophy
  • Ryukyu type of spinal muscular atrophy
  • Bulbospinal muscular atrophy
  • Kennedy Disease
  • Spinal and bulbar muscular atrophy

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

  • 8B61.0 – Infantile spinal muscular atrophy, Type I
  • 8B61.1 – Late infantile spinal muscular atrophy, Type II
  • 8B61.2 – Juvenile form spinal muscular dystrophy, Type III
  • 8B61.3 – Adult onset spinal muscular atrophy, Type IV
  • 8B61.Y – Other specified spinal muscular atrophy
  • 8B61.Z – Spinal muscular atrophy, unspecified

Foundation entity

Localised spinal muscular atrophy – http://id.who.int/icd/entity/870128735

Allowed postcoordination axes

Part of: 8B61: Spinal muscular atrophy › 08: Diseases of the nervous system