Diagnosis Code: G24.1

Short Description: Genetic torsion dystonia

Long Description: Genetic torsion dystonia

The code G24.1 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Extrapyramidal and movement disorders (G20-G26)
    • Dystonia (G24)
      • G24.1 Genetic torsion dystonia

Code Version: 2022 ICD-10-CM

Synonyms

• Acquired torsion dystonia
• Adult-onset familial idiopathic dystonia
• Adult-onset sporadic primary dystonia
• Autosomal dominant dopa responsive dystonia
• Autosomal dominant focal dystonia DYT25 type
• Autosomal dominant idiopathic familial dystonia
• Autosomal recessive dopa responsive dystonia
• Autosomal recessive idiopathic familial dystonia
• Deafness-dystonia-optic neuronopathy syndrome
• Disorder of manganese metabolism
• Diurnal dystonia
• Diurnal dystonia
• Dystonia 6
• Dystonia aphonia syndrome
• Generalized dystonia
• Hypermanganesemia with dystonia
• Hypermanganesemia with dystonia, polycythemia, and cirrhosis
• Idiopathic familial dystonia
• Maternally inherited mitochondrial deoxyribonucleic acid disease
• Maternally inherited mitochondrial dystonia
• Partington syndrome
• Primary dystonia DYT17 type
• Primary dystonia type 4
• Primary torsion dystonia
• Torsion dystonia
• X-linked dystonia parkinsonism

References to Index of Diseases and Injuries

The code G24.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Dystonia deformans progressiva
  • Dystonia musculorum deformans
  • Familial torsion dystonia
  • Idiopathic familial dystonia
  • Idiopathic (torsion) dystonia NOS
  • (Schwalbe-) Ziehen-Oppenheim disease

Crosswalk Information

Similar Codes

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

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