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 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)
- athetoid cerebral palsy (G80.3)
Also Known As / Clinical Terms
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
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.
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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.