Infection causing chorea
Chorea due to cerebral anoxia
Progressive lenticular degeneration
Movements, Choreiform
Ballism
Henoch's chorea
Chorea due to hyponatremia
Kinnier-Wilson disease
Chorea due to Huntington disease-like 2
Hemichorea due to abscess of brain
Hemichorea due to injury of head
Chorea due to Lesch-Nyhan syndrome
Dystonia 9
Chorea with dentatorubropallidoluysian degeneration
Chorea due to immunological disorder
Electric chorea
Hemiballism
Chorea NOS
Choreas
Chorea due to disorder of endocrine system
Chorea due to Henoch-Schönlein purpura
Chorea (disorder)
Choreic movements
Body of Luys syndrome
Disorders, Choreatic
Chorea co-occurrent and due to Wilson disease
Dentatorubropallidoluysian atrophy
Disorder, Chorea
Chorea Syndromes
Chorea due to chronic hepatocerebral degeneration
Hemichorea due to multiple sclerosis
Chorea due to metabolic disorder
Choreatic Syndromes
Syndrome, Chorea
Paroxysmal choreoathetosis
Ballismus
Hemiballismus-hemichorea syndrome
Chorea following injury
Senile chorea
Chorea gravidarum
disorders chorea
Chorea due to antiphospholipid syndrome
Chorea due to thyrotoxicosis
Chorea due to neuroferritinopathy
Hemichorea due to cerebral infarct
Disorder of liver due to disorder of mineral metabolism
Hemiballismus
Chorea Syndrome
Benign hereditary chorea
Cerebellar ataxia associated with another disorder
Childhood-onset benign chorea with striatal involvement
Chorea due to Huntington disease-like 3
chorea
Chorea due to immunoglobulin A vasculitis
Hepatocerebral degeneration
Choreiform movements
Hemichorea due to cerebral hemorrhage
Wilson disease
Syndromes, Choreatic
Chorea with Wilson disease
Chorea due to head injury
Huntington disease-like syndrome disorder
Chronic progressive non-hereditary chorea
chorea disorders
Hemichorea due to cerebral arteriovenous malformation
Early-onset neurodegeneration, choreoathetoid movement, microcytic anaemia due to IREB2 mutation
Chorea due to prion disease
Copper storage disease
Dissociative neurological symptom disorder co-occurrent with chorea
Movement, Choreic
Chorea due to anoxia of brain
Chorea due to cerebral injury due to birth trauma
Syndromes, Chorea
Dubini's chorea
Post-traumatic chorea
Chorea due to and following infective disorder
Chorea due to widespread metastatic malignant neoplastic disease
Chorea due to hereditary ataxia
Progressive chorea
Hepatolenticular degeneration
Huntington disease phenocopy syndrome
Brain lung thyroid syndrome
Chorea due to disseminated malignancy
Chorea due to inborn error of metabolism
Chorea due to hypoparathyroidism
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to IREB2 mutation
NDCAMA - neurodegeneration, choreoathetoid movement, microcytic anemia
Thyrotoxic chorea
Chorea due to endocrine disorder
Choreatic Syndrome
Disorders, Chorea
Infantile convulsion and choreoathetosis syndrome
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration
Chorea due to classical pigmentary pallidal degeneration
chorea disorder
Henoch chorea
Choreic Movement
Parainfectious chorea
Hemichorea due to head injury
Chorea due to classical pantothenate kinase associated neurodegeneration
Myoclonic epilepsy with choreoathetosis
Hemichorea
Paroxysmal kinesigenic dyskinesia
Chorea co-occurrent and due to Huntington disease-like condition
Movements, Choreic
Chorea due to anaphylactoid purpura
Neurohepatic degeneration
Chorea due to Huntington disease-like 1
Chorea due to inherited organic acidemia
Dentatorubral-pallidoluysian atrophy
Disorder of copper metabolism
Paraneoplastic chorea
Chorea due to paraneoplastic syndrome
Infectious chorea
Kinesiogenic choreoathetosis
Post-encephalitic chorea
Disorder, Choreatic
Huntington disease-like syndrome
Paroxysmal dystonia
Chorea due to systemic lupus erythematosus
Chorea due to inherited aminoaciduria
Chorea due to inherited organic acidaemia
Early-onset neurodegeneration, choreoathetoid movement, microcytic anaemia due to iron responsive element binding protein 2 gene mutation
Neurological disorder due to excess intake of micronutrients
Choreatic Disorder
Chorea due to hyperglycemia
Paroxysmal kinesigenic choreoathetosis
Wilson's disease
Syndrome, Choreatic
Paroxysmal kinesigenic dyskinesia and infantile convulsion
Chorea due to heredodegenerative disorder
Hepatolenticular degeneration syndrome
Choreiform disorder
Choreiform Movement
Choreoacanthocytosis
Chorea due to and following ventriculoperitoneal shunt
NDCAMA - neurodegeneration, choreoathetoid movement, microcytic anaemia
Post-hemiplegic chorea
Movement, Choreiform
Chorea due to injury of head
Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome
Copper metabolism disorder
Dentatorubral-pallidoluysian atrophy (DRPLA)
Hemiballism (abnormal involuntary movements)
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity
Toxic chorea
Chorea due to metastatic malignant neoplastic disease
Hemichorea due to neoplasm of brain
Dubini chorea
Choreoathetosis
Chorea due to mitochondrial cytopathy
Oral choreiform movement
Hemichorea due to brain abscess
Chorea due to and following injury of head
Chorea with Huntington disease-like condition
Chorea due to hyperglycaemia
Chorea due to hyponatraemia
CHOREA DIS
Choreatic Disorders
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation
Dubini's disease
Chorea due to ataxia telangiectasia syndrome
Functional chorea
Chorea due to polycythaemia rubra vera
Chorea due to polycythemia rubra vera
Naito-Oyanagi disease
Hemichorea due to cerebral haemorrhage
Dentatorubropallidoluysian degeneration
Paroxysmal dyskinesia
Haw river syndrome
ICCA syndrome
Chorea due to and following encephalitis
Chorea due to classical neurodegeneration with brain iron accumulation type 1
CHOREATIC DIS
DRPLA - Dentatorubropallidoluysian atrophy
WD - Wilson's disease
Hemichorea due to cerebral infarction

Frequently Asked Questions

What is the ICD-10 code for other chorea?

The ICD-10-CM code for other chorea is G25.5. The full clinical description is "Other chorea". G25.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G25.5 mean?

ICD-10-CM code G25.5 represents “Other chorea”. 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 G25.5 a billable code?

Yes, G25.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G25.5 in?

G25.5 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What codes cannot be used with G25.5?

G25.5 has Excludes1 notes indicating codes that cannot be used together with it, including: chorea NOS with heart involvement (I02.0); Huntington's chorea (G10); rheumatic chorea (I02.-); and 1 more.

What SNOMED CT codes does G25.5 map to?

G25.5 maps to 79 SNOMED CT concepts: 426592006, 230306001, 66637005, 719098007, 192874000, and 74 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G25.5?

G25.5 is linked to 2 UMLS Concept Unique Identifiers: C0008489, C0029542. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G25.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other chorea 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 G25.5?

G25.5 maps to the ICD-11 code: 8A0Z (Movement disorders, unspecified).

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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.