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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Nervous System And Sense Organs 320-389 > Hereditary And Degenerative Diseases Of The Central Nervous System 330-337 > Other Extrapyramidal Disease And Abnormal Movement Disorders 333.* >

2008 ICD-9-CM Diagnosis 333.4

Huntington's chorea

  • A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)
  • KEGG_ID: hsa05040
  • 333.4 is a specific code that can be used to specify a diagnosis
  • 333.4 contains 9 index entries
  • View the ICD-9-CM Volume 1 333.* hierarchy


Index entries containing 333.4:

Chorea (gravis) (minor) (spasmodic) 333.5
  • chronic 333.4
  • hereditary 333.4
  • Huntington's 333.4
  • progressive 333.4
    • chronic 333.4
    • hereditary 333.4
Disease, diseased - see also Syndrome
  • Huntington's 333.4
Huntington's
  • chorea 333.4
  • disease 333.4