G25.89

Billable

Other specified extrapyramidal and movement disorders

Other specified extrapyramidal and movement disorders

Status

Billable / Specific

Block

G20-G26

Parent Code

G25.8

Coding Notes

Related Codes(3)
Also Known As / Clinical Terms(152)

SNOMED CT

Clinical Terms

  • Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
  • Restlessness
  • Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
  • Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome
  • Jumpy stump syndrome
  • Paroxysmal nonkinesigenic dyskinesia
  • Paroxysmal choreoathetosis
  • Mirror movements
  • Familial paroxysmal choreoathetosis
  • Proximal myopathy
  • Autoimmune movement disorder
  • Biotin-responsive basal ganglia disease
  • Proximal myopathy with extrapyramidal signs
  • Motor restlessness
  • GNAO1-related spectrum
  • Hereditary congenital mirror movements
  • Pallidonigral atrophy
  • Benign Rolandic epilepsy
  • Self-limited epilepsy with centrotemporal spikes
  • Restlessness behavior
  • SYT1-related neurodevelopmental disorder
  • Progressive chorea
  • Recessive intellectual disability, motor dysfunction, multiple joint contractures syndrome
  • Disorders of spinal neurones manifest by hyperactivity
  • Grimace
  • Restlessness behaviour
  • X-linked intellectual disability, hypotonia, movement disorder syndrome
  • Progressive chorea-cerebellar atrophy syndrome
  • Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
  • Childhood epilepsy with centrotemporal spikes
  • Primary progressive freezing gait syndrome
  • Baker Gordon syndrome
  • Familial congenital controlateral synkinesia
  • Lhermitte AND McAlpine syndrome
  • Isolated congenital mirror movements
  • Akathisia
  • Birnbaum syndrome
  • Familial congenital mirror movements
  • Organic writer's cramp
  • Isolated congenital controlateral synkinesia
  • SeLECTS - self-limited epilepsy with centrotemporal spikes
  • Paroxysmal dystonia
  • G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum
  • Combined pyramidal-extrapyramidal syndrome
  • Hereditary congenital controlateral synkinesia
  • Occupational dystonia
  • Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
  • Writers' spasm
  • Birnbaum's syndrome
  • Synaptotagmin 1-related neurodevelopmental disorder
  • Truncal ataxia
  • Scriveners' palsy
  • Writers' paralysis
  • Primary progressive freezing gait
  • Graphospasm
  • Mount-Reback syndrome
  • Pallidonigral degeneration
  • Writers' cramp
  • Benign epilepsy of childhood with centro-temporal spikes
  • Paradoxical facial movements
  • Thiamine transporter-2 deficiency
  • GNAO1-related developmental delay, seizures, movement disorder spectrum
  • Choreoathetosis
  • Paralysis notariorum
  • Autoimmune disorder of movement
  • Grimaces
  • Writer's cramp
  • Bobble-head doll syndrome
  • Paroxysmal dyskinesia
  • Akinetic rigid syndrome
  • Biotin-thiamine-responsive basal ganglia disease
  • Thiamine metabolism dysfunction syndrome 2
  • Organic writers' cramp
  • Pallidal degeneration
  • Paroxysmal dystonic choreoathetosis
Frequently Asked Questions
What is the ICD-10 code for other specified extrapyramidal and movement disorders?

The ICD-10-CM code for other specified extrapyramidal and movement disorders is G25.89. The full clinical description is "Other specified extrapyramidal and movement disorders". G25.89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G25.89 mean?

ICD-10-CM code G25.89 represents “Other specified extrapyramidal and movement disorders”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.

Is G25.89 a billable code?

Yes, G25.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G25.89 in?

G25.89 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What SNOMED CT codes does G25.89 map to?

G25.89 maps to 35 SNOMED CT concepts: 285145004, 413100008, 1259084000, 770901001, 1217371005, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G25.89?

G25.89 is linked to 1 UMLS Concept Unique Identifier: C0477362. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G25.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified extrapyramidal and movement disorders affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of G25.89?

There is no direct ICD-11 mapping available for G25.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.