G24.8
BillableOther dystonia
Other dystonia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Acquired torsion dystonia 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(203)
SNOMED CT
- Facial myokymia1070000
- Facial myokymia (muscle quivering)1070000
- 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
- Orofacial dyskinesia49386006
- Dystonia lenticularis52274002
- Fragments of torsion dystonia192859002
- Paroxysmal dystonia230310003
- Genetic torsion dystonia230318005
- Idiopathic familial dystonia230318005
- Autosomal dominant idiopathic familial dystonia230319002
- Autosomal recessive idiopathic familial dystonia230320008
- Isolated cervical dystonia230322000
- Posthemiplegic dystonia230329009
- Occupational dystonia230330004
- Diurnal dystonia230332007
- Dopa responsive dystonia230332007
- Levodopa-responsive dystonia230332007
- Segawa dystonia230332007
- Sleep-related dystonia230500006
- Familial progressive cerebral sclerosis396338004
- MLD - Metachromatic leucodystrophy396338004
- Metachromatic leucodystrophy396338004
- Metachromatic leukodystrophy396338004
- Metachromatic leukoencephaly396338004
- Sulfatide lipidosis396338004
- Sulphatide lipidosis396338004
- van Bogaert-Nijssen disease396338004
- Generalised dystonia425492002
- Generalized dystonia425492002
- Hemidystonia427232004
- Segmental dystonia427945008
- Acquired torsion dystonia433493000
- Myoclonic dystonia439732004
- Cranial dystonia443352005
- Dystonia of head443352005
- Focal dystonia445006008
- Primary dystonia DYT2 type715777007
- Primary dystonia type 2715777007
- Primary dystonia 21716664003
- Primary dystonia DYT21 type716664003
- Brain dopamine-serotonin vesicular transport disease717942003
- Primary dystonia DYT13 type719278006
- Primary dystonia type 13719278006
- Primary dystonia with mixed phenotype719278006
- Dystonia 16722435003
- Early-onset dystonia parkinsonism722435003
- Dystonia 18724072002
- Paroxysmal exertion-induced dyskinesia724072002
- Hemidystonia hemiatrophy syndrome724383002
- FDFM - familial dyskinesia and facial myokymia763352005
- Familial dyskinesia and facial myokymia763352005
- Cranio-cervical dystonia with laryngeal and upper limb involvement783179009
- DYT24 - dystonia 24783179009
- Dystonia 24783179009
- Toxic dystonia840501003
- Infantile-onset generalised dyskinesia with orofacial involvement1172603005
- Infantile-onset generalized dyskinesia with orofacial involvement1172603005
- Infantile-onset orofacial, trunk, limbs dyskinesia1172603005
- Dystonia due to Leigh syndrome1187533007
- Dopa responsive dystonia due to sepiapterin reductase deficiency1187545003
- Primary dystonia DYT27 type1220573009
- Primary dystonia type 271220573009
- Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome1231737000
- Dystonia due to disorder of peripheral nervous system1260331001
- Dystonia due to anoxia of brain1260332008
- Dystonia due to cerebral anoxia1260332008
- Dystonia due to ataxia telangiectasia syndrome1260334009
- Dystonia due to ataxia-telangiectasia syndrome1260334009
- Dystonia due to focal brain lesion1260339004
- Dystonia due to Fahr syndrome1260341003
- Dystonia due to familial basal ganglia calcifications1260341003
- Dystonia due to encephalitis1260343000
- Dystonia due to atypical pantothenate kinase associated neurodegeneration1260360005
- Dystonia due to atypical pigmentary pallidal degeneration1260360005
- Dystonia in neurodegeneration with brain iron accumulation type 11260360005
- Dystonia due to Rett syndrome1260362002
- Dystonia due to Pelizaeus-Merzbacher disease1260363007
- Dystonia due to mitochondrial cytopathy1260365000
- Dystonia due to mitochondrial disease1260365000
- Dystonia due to Niemann-Pick disease type C1260366004
- Dystonia due to metachromatic leucodystrophy1260391004
- Dystonia due to metachromatic leukodystrophy1260391004
- Dystonia due to hereditary disease1260396009
- Dystonia due to inherited disorder1260396009
- Dystonia due to hereditary spastic paraplegia1260397000
- Dystonia due to homocystinuria1260398005
- Dystonia due to Hartnup disease1260399002
- Dystonia due to neutral 1 amino acid transport defect1260399002
- Dystonia due to head injury1260400009
- DYT28 - dystonia 281281844004
- Dystonia 281281844004
- KMT2B-related dystonia1281844004
- Lysine methyltransferase 2B-related dystonia1281844004
- Laryngeal dystonia3331000119108
UMLS
Clinical Terms
- Primary dystonia type 2
- Dystonia due to disorder of peripheral nervous system
- Dystonia due to ataxia-telangiectasia syndrome
- Laryngeal dystonia
- Toxic dystonia
- Sleep-related dystonia
- Acquired torsion dystonia
- Dystonia 18
- Dystonia due to homocystinuria
- Dystonia due to hereditary spastic paraplegia
- Dystonia due to familial basal ganglia calcifications
- Myoclonic dystonia
- Dystonia of head
- Idiopathic familial dystonia
- Autosomal recessive idiopathic familial dystonia
- Infantile-onset generalised dyskinesia with orofacial involvement
- Dystonia due to ataxia telangiectasia syndrome
- Facial myokymia
- Primary dystonia type 13
- Dystonia due to focal brain lesion
- Dystonia due to Fahr syndrome
- Dystonia due to mitochondrial cytopathy
- Dystonia due to Rett syndrome
- Dystonia due to Niemann-Pick disease type C
- MLD - Metachromatic leucodystrophy
- Orofacial dyskinesia
- Acquired torsion dystonia NOS
- Dystonia in neurodegeneration with brain iron accumulation type 1
- Dystonia due to Hartnup disease
- Dystonia 28
- Benign Rolandic epilepsy
- Self-limited epilepsy with centrotemporal spikes
- Sulphatide lipidosis
- Focal dystonia
- van Bogaert-Nijssen disease
- Levodopa-responsive dystonia
- Primary dystonia 21
- FDFM - familial dyskinesia and facial myokymia
- Dystonia 24
- Infantile-onset orofacial, trunk, limbs dyskinesia
- Dystonia due to neutral 1 amino acid transport defect
- Cranio-cervical dystonia with laryngeal and upper limb involvement
- Dystonia due to mitochondrial disease
- Metachromatic leukodystrophy
- Childhood epilepsy with centrotemporal spikes
- Paroxysmal exertion-induced dyskinesia
- Isolated cervical dystonia
- DYT28 - dystonia 28
- Hemidystonia hemiatrophy syndrome
- Hemidystonia
- Dopa responsive dystonia due to sepiapterin reductase deficiency
- Facial myokymia (muscle quivering)
- SeLECTS - self-limited epilepsy with centrotemporal spikes
- Early-onset dystonia parkinsonism
- Infantile-onset generalized dyskinesia with orofacial involvement
- Primary dystonia DYT21 type
- Paroxysmal dystonia
- Dystonia due to metachromatic leukodystrophy
- Familial dyskinesia and facial myokymia
- Fragments of torsion dystonia
- Occupational dystonia
- Posthemiplegic dystonia
- Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
- Lysine methyltransferase 2B-related dystonia
- Metachromatic leukoencephaly
- Primary dystonia type 27
- Dystonia lenticularis
- KMT2B-related dystonia
- Dystonia due to anoxia of brain
- Generalised dystonia
- Dystonia due to atypical pantothenate kinase associated neurodegeneration
- Sulfatide lipidosis
- Primary dystonia with mixed phenotype
- Dystonia due to head injury
- Dystonia due to inherited disorder
- Acquired torsion dystonia (disorder)
- Segawa dystonia
- Autosomal dominant idiopathic familial dystonia
- Generalized dystonia
- Cranial dystonia
- Benign epilepsy of childhood with centro-temporal spikes
- Primary dystonia DYT13 type
- Dystonia due to hereditary disease
- Primary dystonia DYT2 type
- Familial progressive cerebral sclerosis
- DYT24 - dystonia 24
- Dystonia due to atypical pigmentary pallidal degeneration
- Dystonia due to Pelizaeus-Merzbacher disease
- Primary dystonia DYT27 type
- Brain dopamine-serotonin vesicular transport disease
- Dystonia due to encephalitis
- Diurnal dystonia
- Dystonia due to metachromatic leucodystrophy
- Metachromatic leucodystrophy
- Dystonia 16
- Genetic torsion dystonia
- Dystonia due to cerebral anoxia
- Segmental dystonia
- Dopa responsive dystonia
- Dystonia due to Leigh syndrome
Frequently Asked Questions
What is the ICD-10 code for other dystonia?
The ICD-10-CM code for other dystonia is G24.8. The full clinical description is "Other dystonia". G24.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G24.8 mean?
ICD-10-CM code G24.8 represents “Other dystonia”. 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 G24.8 a billable code?
Yes, G24.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G24.8 in?
G24.8 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G24.8 map to?
G24.8 maps to 56 SNOMED CT concepts: 433493000, 230319002, 230320008, 44145005, 717942003, and 51 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G24.8?
G24.8 is linked to 2 UMLS Concept Unique Identifiers: C1719382, C0477360. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G24.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other dystonia 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 G24.8?
G24.8 maps to the ICD-11 code: 8A02.Z (Dystonic 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.