G25.89
BillableOther specified extrapyramidal and movement disorders
Other specified extrapyramidal and movement disorders
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •sleep related movement disordersG47.6
Related Codes(3)
Also Known As / Clinical Terms(152)
SNOMED CT
- Grimace39960009
- Grimaces39960009
- Choreoathetosis43105007
- Benign Rolandic epilepsy44145005
- Benign epilepsy of childhood with centro-temporal spikes44145005
- Childhood epilepsy with centrotemporal spikes44145005
- SeLECTS - self-limited epilepsy with centrotemporal spikes44145005
- Self-limited epilepsy with centrotemporal spikes44145005
- Birnbaum syndrome45814002
- Birnbaum's syndrome45814002
- Progressive chorea-cerebellar atrophy syndrome45814002
- Paroxysmal choreoathetosis49949003
- Paroxysmal dyskinesia49949003
- Graphospasm52008007
- Organic writer's cramp52008007
- Organic writers' cramp52008007
- Paralysis notariorum52008007
- Scriveners' palsy52008007
- Writer's cramp52008007
- Writers' cramp52008007
- Writers' paralysis52008007
- Writers' spasm52008007
- Paradoxical facial movements69233001
- Combined pyramidal-extrapyramidal syndrome75046006
- Lhermitte AND McAlpine syndrome75046006
- Pallidonigral atrophy80180004
- Pallidonigral degeneration80180004
- Motor restlessness162221009
- Restlessness162221009
- Restlessness behavior162221009
- Restlessness behaviour162221009
- Proximal myopathy193255007
- Mirror movements229247004
- Pallidal degeneration230302004
- Paroxysmal dystonia230310003
- Occupational dystonia230330004
- Disorders of spinal neurones manifest by hyperactivity230651008
- Truncal ataxia250067008
- Akathisia285145004
- Akinetic rigid syndrome413100008
- Familial paroxysmal choreoathetosis609218006
- Mount-Reback syndrome609218006
- Paroxysmal dystonic choreoathetosis609218006
- Paroxysmal nonkinesigenic dyskinesia609218006
- Biotin-responsive basal ganglia disease703522009
- Biotin-thiamine-responsive basal ganglia disease703522009
- Thiamine metabolism dysfunction syndrome 2703522009
- Thiamine transporter-2 deficiency703522009
- Primary progressive freezing gait715627004
- Primary progressive freezing gait syndrome715627004
- Proximal myopathy with extrapyramidal signs770722002
- Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome770901001
- Recessive intellectual disability, motor dysfunction, multiple joint contractures syndrome770901001
- Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome782886007
- Familial congenital controlateral synkinesia784348007
- Familial congenital mirror movements784348007
- Hereditary congenital controlateral synkinesia784348007
- Hereditary congenital mirror movements784348007
- Isolated congenital controlateral synkinesia784348007
- Isolated congenital mirror movements784348007
- Intellectual disability, hyperkinetic movement, truncal ataxia syndrome787174003
- Baker Gordon syndrome1217371005
- Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome1217371005
- SYT1-related neurodevelopmental disorder1217371005
- Synaptotagmin 1-related neurodevelopmental disorder1217371005
- Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome1231737000
- X-linked intellectual disability, hypotonia, movement disorder syndrome1254654006
- Bobble-head doll syndrome1259031004
- Autoimmune disorder of movement1259084000
- Autoimmune movement disorder1259084000
- Jumpy stump syndrome1263542005
- G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum1281842000
- GNAO1-related developmental delay, seizures, movement disorder spectrum1281842000
- GNAO1-related spectrum1281842000
- Progressive chorea27751000119104
UMLS
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.