Diagnosis Code: 334.2

Short Description: Primary cerebellar degen

Long Description: Primary cerebellar degeneration

Code Classification:

• Diseases of the nervous system (320–359)
  • Hereditary and degenerative diseases of the central nervous system (330-337)
    • 334 Spinocerebellar disease
      • 334.2 Primary cerebellar degen

Code Version: 2015 ICD-9-CM

References to Index of Diseases and Injuries

The code 334.2 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Ataxia, ataxy, ataxic 781.3
  • cerebellar 334.3
    • hereditary (Marie's) 334.2
  • family, familial 334.2
    • cerebral (Marie's) 334.2
    • spinal (Friedreich's) 334.0
  • hereditary NEC 334.2
    • cerebellar 334.2
    • spastic 334.1
    • spinal 334.0
  • heredofamilial (Marie's) 334.2
  • Marie's (cerebellar) (heredofamilial) 334.2
  • Sanger-Brown's 334.2

• Degeneration, degenerative
  • cerebellar NEC 334.9
    • primary (hereditary) (sporadic) 334.2
  • cortical (cerebellar) (parenchymatous) 334.2
    • alcoholic 303.9 [334.4]
    • diffuse, due to arteriopathy 437.0

• Disease, diseased - see also Syndrome
  • Hunt's
    • dyssynergia cerebellaris myoclonica 334.2

• Dyssynergia
  • cerebellaris myoclonica 334.2

• Hunt's
  • syndrome (herpetic geniculate ganglionitis) 053.11
    • dyssynergia cerebellaris myoclonica 334.2

• Marie's
  • cerebellar ataxia 334.2

• Ramsay Hunt syndrome (herpetic geniculate ganglionitis) 053.11
  • meaning dyssynergia cerebellaris myoclonica 334.2

• Sanger-Brown's ataxia 334.2

• Sclerosis, sclerotic
  • brain (general) (lobular) 348.89
    • hereditary 334.2
  • hereditary
    • cerebellar 334.2

• Syndrome - see also Disease
  • Hunt's (herpetic geniculate ganglionitis) 053.11
    • dyssynergia cerebellaris myoclonica 334.2
  • Ramsay Hunt's
    • dyssynergia cerebellaris myoclonica 334.2

Crosswalk Information

The code 334.2 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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