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 period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- sleep related movement disorders (G47.6-)
Also Known As / Clinical Terms
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
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.
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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.