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2007 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 330-338 > Other Extrapyramidal Disease And Abnormal Movement Disorders 333.* >

2007 ICD-9-CM Diagnosis 333.6

Genetic torsion dystonia

This code may be outdated. View the most recent version of ICD-9-CM 333.6

  • A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)
  • 333.6 is a specific code that can be used to specify a diagnosis
  • 333.6 contains 12 index entries
  • View the ICD-9-CM Volume 1 333.* hierarchy

333.6 also known as:

  • Dystonia:
    • deformans progressiva
    • musculorum deformans
  • (Schwalbe-) Ziehen-Oppenheim disease

Index entries containing 333.6:

Athetosis (acquired) 781.0
  • congenital (bilateral) 333.6
Disease, diseased - see also Syndrome
  • Schwalbe-Ziehen-Oppenheimer 333.6
  • Ziehen-Oppenheim 333.6
Dysbasia 719.7
  • lordotica (progressiva) 333.6
Dystonia
  • deformans progressiva 333.6
  • lenticularis 333.6
  • musculorum deformans 333.6
  • torsion (idiopathic) 333.6
Schwalbe-Ziehen-Oppenheimer disease 333.6
Spasm, spastic, spasticity (see also condition) 781.0
  • torsion 333.6
Ziehen-Oppenheim disease 333.6