G24.9
BillableDystonia, unspecified
Dystonia, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dyskinesia NOS
Includes
Conditions included under this code
- dyskinesia
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
- •athetoid cerebral palsyG80.3
Related Codes(7)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(142)
SNOMED CT
- Dyskinesia9748009
- Dystonia15802004
- Dystonia disorder15802004
- Adiadochokinesia61691009
- Adiadochokinesis61691009
- Adiadokokinesia61691009
- Adiadokokinesis61691009
- Disorder of manganese metabolism63656007
- Cochlear hearing loss85571008
- Inner ear hearing loss85571008
- Sensory hearing loss85571008
- Neonatal dyskinesia95630007
- Generalised dystonia425492002
- Generalized dystonia425492002
- DYT12 - dystonia 12702323008
- Dystonia 12702323008
- Rapid onset dystonia parkinsonism702323008
- Generalised epilepsy and paroxysmal dyskinesia syndrome715629001
- Generalized epilepsy and paroxysmal dyskinesia syndrome715629001
- Adult-onset dystonia parkinsonism720466001
- Dystonia parkinsonism Paisan-Ruiz type720466001
- PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism720466001
- Developmental malformation, deafness, dystonia syndrome721092005
- Dopamine transporter deficiency syndrome722763000
- Infantile dystonia parkinsonism722763000
- Parkinsonism-dystonia infantile722763000
- Functional dystonia724822003
- Leucoencephalopathy, dystonia, motor neuropathy syndrome733452000
- Leukoencephalopathy, dystonia, motor neuropathy syndrome733452000
- Progressive myoclonic epilepsy with dystonia763349002
- Progressive myoclonus epilepsy with dystonia763349002
- Familial manganese-induced neurotoxicity768553002
- HMNDYT - hypermanganesemia with dystonia768553002
- Hypermanganesemia with dystonia768553002
- HMNDYT2 - hypermanganesemia with dystonia 2768554008
- Hypermanganesemia with dystonia 2768554008
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome770751003
- Dissociative neurological symptom disorder co-occurrent with dystonia788908000
- Functional neurological symptom disorder with dystonia788908000
- Dystonia due to perinatal cerebral injury1260364001
- Dystonia due to glutaric acidaemia1260378000
- Dystonia due to glutaric acidemia1260378000
- Dystonia due to GM2 gangliosidosis1260380006
- Dystonia due to Lesch Nyhan syndrome1260390003
- Dystonia due to head injury1260400009
- Dystonia due to Wilson disease1263524000
- Dystonia of left hand15985831000119107
- Dystonia of right hand15985791000119101
UMLS
- Abnormal MovementC0013384
- Abnormal MovementsC0013384
- Disorder of involuntary muscle movementsC0013384
- DyscinesiaC0013384
- DyskinesiaC0013384
- Dyskinesia (finding)C0013384
- Dyskinesia NOSC0013384
- DyskinesiasC0013384
- DyskinesisC0013384
- Dyskinetic syndromeC0013384
- Movement, AbnormalC0013384
- Movements, AbnormalC0013384
- Syndrome dyskineticC0013384
- dyskinesiaC0013384
- DYSTONIA DISC0393593
- DYSTONIC DISC0393593
- DystoniaC0393593
- Dystonia (disorder)C0393593
- Dystonia DisorderC0393593
- Dystonia DisordersC0393593
- Dystonia disorderC0393593
- Dystonia, unspecifiedC0393593
- Dystonic DisorderC0393593
- Dystonic DisordersC0393593
- Dystonic diseaseC0393593
- dystoniaC0393593
- dystonic disorderC0393593
- dystonic disordersC0393593
Clinical Terms
- Hypermanganesemia with dystonia 2
- Dystonia Disorders
- HMNDYT2 - hypermanganesemia with dystonia 2
- Dissociative neurological symptom disorder co-occurrent with dystonia
- Dystonia due to Wilson disease
- Disorder of manganese metabolism
- Abnormal Movements
- Adiadokokinesia
- Neonatal dyskinesia
- Abnormal Movement
- Dystonia due to head injury
- Dystonia of right hand
- DYT12 - dystonia 12
- Dystonia due to perinatal cerebral injury
- Leucoencephalopathy, dystonia, motor neuropathy syndrome
- Adiadochokinesia
- Dystonic Disorder
- Dyscinesia
- Dystonia (disorder)
- Movements, Abnormal
- Dystonia due to glutaric acidemia
- Generalized epilepsy and paroxysmal dyskinesia syndrome
- Generalized dystonia
- DYSTONIC DIS
- Dyskinesis
- Dystonia due to GM2 gangliosidosis
- Dystonia of left hand
- Dyskinesia
- Adult-onset dystonia parkinsonism
- Movement, Abnormal
- Adiadochokinesis
- Sensory hearing loss
- Dystonic disease
- Hypermanganesemia with dystonia
- Progressive myoclonus epilepsy with dystonia
- Dyskinesia (finding)
- Parkinsonism-dystonia infantile
- PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism
- Dystonia due to Lesch Nyhan syndrome
- Dystonia due to glutaric acidaemia
- Progressive myoclonic epilepsy with dystonia
- Dyskinesias
- Syndrome dyskinetic
- Dystonia parkinsonism Paisan-Ruiz type
- Familial manganese-induced neurotoxicity
- Rapid onset dystonia parkinsonism
- HMNDYT - hypermanganesemia with dystonia
- Inner ear hearing loss
- Dystonia Disorder
- Dyskinetic syndrome
- dystonic disorders
- Dystonia 12
- Disorder of involuntary muscle movements
- Dyskinesia NOS
- Adiadokokinesis
- Dopamine transporter deficiency syndrome
- Functional dystonia
- Cochlear hearing loss
- Functional neurological symptom disorder with dystonia
- Leukoencephalopathy, dystonia, motor neuropathy syndrome
- DYSTONIA DIS
- Developmental malformation, deafness, dystonia syndrome
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
- Generalised dystonia
- Infantile dystonia parkinsonism
- Generalised epilepsy and paroxysmal dyskinesia syndrome
Frequently Asked Questions
What is the ICD-10 code for dystonia, unspecified?
The ICD-10-CM code for dystonia, unspecified is G24.9. The full clinical description is "Dystonia, unspecified". G24.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G24.9 mean?
ICD-10-CM code G24.9 represents “Dystonia, unspecified”. 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 G24.9 a billable code?
Yes, G24.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G24.9 in?
G24.9 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G24.9 map to?
G24.9 maps to 27 SNOMED CT concepts: 61691009, 720466001, 85571008, 702323008, 721092005, and 22 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G24.9?
G24.9 is linked to 2 UMLS Concept Unique Identifiers: C0013384, C0393593. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G24.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like dystonia, unspecified 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 G24.9?
G24.9 maps to the ICD-11 code: 8A02.0Z (Primary dystonia, 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.