G24.1
BillableGenetic torsion dystonia
Genetic torsion dystonia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dystonia deformans progressiva
- Dystonia musculorum deformans
- Familial torsion dystonia
- Idiopathic familial dystonia
- Idiopathic (torsion) dystonia NOS
- (Schwalbe-) Ziehen-Oppenheim disease
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
- Dystonia deformans progressiva22451001
- Dystonia musculorum deformans22451001
- Idiopathic torsion dystonia22451001
- Primary torsion dystonia22451001
- Schwalbe disease22451001
- Ziehen-Oppenheim disease22451001
- Disorder of manganese metabolism63656007
- Genetic torsion dystonia230318005
- Idiopathic familial dystonia230318005
- Autosomal dominant idiopathic familial dystonia230319002
- Autosomal recessive idiopathic familial dystonia230320008
- Diurnal dystonia230332007
- Dopa responsive dystonia230332007
- Levodopa-responsive dystonia230332007
- Segawa dystonia230332007
- Generalised dystonia425492002
- Generalized dystonia425492002
- Torsion dystonia431034009
- Acquired torsion dystonia433493000
- Lubag698279003
- Torsion dystonia parkinsonism Filipino type698279003
- X-linked dystonia parkinsonism698279003
- X-linked torsion dystonia parkinsonism syndrome698279003
- XDP - X-linked dystonia parkinsonism698279003
- HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis702377007
- HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythaemia, and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis702377007
- Partington X-linked intellectual disability syndrome702412005
- Partington syndrome702412005
- Partington x-linked mental retardation syndrome702412005
- Partington-Mulley syndrome702412005
- X-linked intellectual deficit-dystonia-dysarthria syndrome702412005
- Deafness-dystonia syndrome702423009
- Deafness-dystonia-optic neuronopathy syndrome702423009
- Mohr-Tranebjaerg syndrome702423009
- Dystonia 6702448007
- Idiopathic torsion dystonia of mixed type702448007
- Primary dystonia, DYT6 type702448007
- THAP1 dystonia702448007
- Torsion dystonia 6702448007
- Autosomal dominant Segawa syndrome715768000
- Autosomal dominant dopa responsive dystonia715768000
- Hereditary progressive dystonia with marked diurnal fluctuation715768000
- Autosomal recessive Segawa syndrome715827001
- Autosomal recessive dopa responsive dystonia715827001
- Tyrosine hydroxylase deficiency715827001
- Tyrosine hydroxylase deficient dopa responsive dystonia715827001
- Maternally inherited mitochondrial dystonia717054001
- Hereditary whispering dysphonia719276005
- Primary dystonia DYT4 type719276005
- Primary dystonia type 4719276005
- Autosomal dominant focal dystonia DYT25 type719516000
- Familial manganese-induced neurotoxicity768553002
- HMNDYT - hypermanganesemia with dystonia768553002
- Hypermanganesemia with dystonia768553002
- Primary dystonia DYT17 type782695002
- Dystonia aphonia syndrome782718007
- Adult-onset familial idiopathic dystonia1259061007
- Adult-onset familial primary dystonia1259061007
- Adult-onset sporadic primary dystonia1259072002
- IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome1303273003
- Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome1303273003
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome1332508004
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome1332508004
- CIMDAG syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome1332508004
UMLS
- (Schwalbe-) Ziehen-Oppenheim diseaseC0013423
- CHILDHOOD TORTION DISC0013423
- Childhood Torsion DiseaseC0013423
- Dystonia Deformans MusculorumC0013423
- Dystonia Deformans ProgressivaC0013423
- Dystonia Musculorum DeformansC0013423
- Dystonia deformans progressivaC0013423
- Dystonia musculorum deformansC0013423
- Dystonias, TorsionC0013423
- OPPENHEIM ZIEHEN DISC0013423
- Oppenheim Ziehen DiseaseC0013423
- Oppenheim-Ziehen DiseaseC0013423
- Progressive Torsion SpasmC0013423
- Spasm, Progressive TorsionC0013423
- TORSION DIS CHILDHOODC0013423
- Torsion Disease of ChildhoodC0013423
- Torsion Disease, ChildhoodC0013423
- Torsion DystoniaC0013423
- Torsion Spasm, ProgressiveC0013423
- Torsion dystoniaC0013423
- Torsion dystonia (disorder)C0013423
- Ziehen Oppenheim diseaseC0013423
- dystonia deformans progressivaC0013423
- dystonia musculorum deformansC0013423
- idiopathic torsion dystoniaC0013423
- torsion dystoniaC0013423
- Dystonia, Idiopathic FamilialC0393598
- Dystonias, Idiopathic FamilialC0393598
- Familial Dystonia, IdiopathicC0393598
- Familial Dystonias, IdiopathicC0393598
- Familial Idiopathic DystoniaC0393598
- Idiopathic Familial DystoniaC0393598
- Idiopathic Familial DystoniasC0393598
- Idiopathic familial dystoniaC0393598
- Idiopathic familial dystonia (disorder)C0393598
- Dystonia, Idiopathic TorsionC5848258
- Dystonias, Idiopathic TorsionC5848258
- Idiopathic (torsion) dystonia NOSC5848258
- Idiopathic Torsion DystoniaC5848258
- Idiopathic Torsion DystoniasC5848258
- Idiopathic torsion dystoniaC5848258
- Idiopathic torsion dystonia (disorder)C5848258
- Primary torsion dystoniaC5848258
- Schwalbe diseaseC5848258
- Torsion Dystonia, IdiopathicC5848258
- Ziehen-Oppenheim diseaseC5848258
- Familial torsion dystoniaC2875058
- Genetic Torsion DystoniaC5779546
- Genetic torsion dystoniaC5779546
Frequently Asked Questions
What is ICD-10 code G24.1?
ICD-10-CM code G24.1 represents "Genetic torsion dystonia". It is a billable/specific code that can be used on a claim.
Is G24.1 a billable code?
Yes, G24.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G24.1 in?
G24.1 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G24.1 map to?
G24.1 maps to 26 SNOMED CT concepts: 433493000, 1259061007, 1259072002, 715768000, 719516000, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G24.1?
G24.1 is linked to 5 UMLS Concept Unique Identifiers: C0013423, C0393598, C5848258, C2875058, C5779546. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.