Diagnosis Code: G12.1

Short Description: Other inherited spinal muscular atrophy

Long Description: Other inherited spinal muscular atrophy

The code G12.1 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Systemic atrophies primarily affecting the central nervous system (G10-G14)
    • Spinal muscular atrophy and related syndromes (G12)
      • G12.1 Other inherited spinal muscular atrophy

Code Version: 2022 ICD-10-CM

Synonyms

• Adult spinal muscular atrophy
• Autosomal dominant adult-onset proximal spinal muscular atrophy
• Autosomal dominant congenital benign spinal muscular atrophy
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal recessive distal hereditary motor neuropathy
• Autosomal recessive distal hereditary motor neuropathy
• Autosomal recessive distal hereditary motor neuropathy
• Autosomal recessive distal spinal muscular atrophy type 3
• Congenital anterior polar cataract
• Dandy-Walker syndrome
• Distal hereditary motor neuropathy Jerash type
• Distal spinal muscular atrophy
• Distal spinal muscular atrophy
• Distal spinal muscular atrophy
• Distal spinal muscular atrophy
• Distal spinal muscular atrophy
• Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
• Kugelberg-Welander disease
• Progressive bulbar palsy
• Progressive bulbar palsy
• Progressive bulbar palsy of childhood
• Progressive muscular atrophy
• Scapulohumeral spinal muscular atrophy
• Scapuloperoneal spinal muscular atrophy
• Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• Spinal muscular atrophy
• Spinal muscular atrophy with lower extremity predominance
• Spinal muscular atrophy with respiratory distress type 1
• Spinal muscular atrophy with respiratory distress type 2
• Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
• Spinal muscular atrophy, type II
• Upper motor neuron disease
• Upper motor neuron disease
• X-linked distal hereditary motor neuropathy
• X-linked distal hereditary motor neuropathy
• X-linked distal spinal muscular atrophy type 3

References to Index of Diseases and Injuries

The code G12.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Adult form spinal muscular atrophy
  • Childhood form, type II spinal muscular atrophy
  • Distal spinal muscular atrophy
  • Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
  • Progressive bulbar palsy of childhood [Fazio-Londe]
  • Scapuloperoneal form spinal muscular atrophy

Crosswalk Information

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This page was last updated on: 10/1/2023

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