AutoICD API

G24.1

Billable

Genetic torsion dystonia

Genetic torsion dystonia

Status

Billable / Specific

Block

G20-G26

Parent Code

G24

ICD-11 Mapping

1 equivalent

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

Related Codes(7)
G24.0

Drug induced dystonia

G24.2

Idiopathic nonfamilial dystonia

BillableG24.3

Spasmodic torticollis

BillableG24.4

Idiopathic orofacial dystonia

BillableG24.5

Blepharospasm

BillableG24.8

Other dystonia

BillableG24.9

Dystonia, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

8A02.0ZPrimary dystonia, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(214)

SNOMED CT

UMLS

Clinical Terms

  • Hereditary whispering dysphonia
  • Torsion Disease, Childhood
  • Primary dystonia DYT4 type
  • Dystonia, Idiopathic Torsion
  • dystonia musculorum deformans
  • Acquired torsion dystonia
  • Torsion Disease of Childhood
  • Hypermanganesemia with dystonia
  • Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome
  • CHILDHOOD TORTION DIS
  • Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
  • Idiopathic familial dystonia
  • Autosomal dominant focal dystonia DYT25 type
  • Idiopathic torsion dystonia (disorder)
  • Autosomal recessive idiopathic familial dystonia
  • Oppenheim-Ziehen Disease
  • Primary dystonia, DYT6 type
  • Torsion dystonia 6
  • CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome
  • Levodopa-responsive dystonia
  • Familial Idiopathic Dystonia
  • Idiopathic torsion dystonia
  • Idiopathic torsion dystonia of mixed type
  • HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis
  • Oppenheim Ziehen Disease
  • dystonia deformans progressiva
  • HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis
  • XDP - X-linked dystonia parkinsonism
  • torsion dystonia
  • Ziehen-Oppenheim disease
  • Dystonias, Idiopathic Torsion
  • Adult-onset sporadic primary dystonia
  • OPPENHEIM ZIEHEN DIS
  • Autosomal dominant dopa responsive dystonia
  • Deafness-dystonia-optic neuronopathy syndrome
  • Maternally inherited mitochondrial dystonia
  • IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
  • Torsion Dystonia, Idiopathic
  • Deafness-dystonia syndrome
  • (Schwalbe-) Ziehen-Oppenheim disease
  • Progressive Torsion Spasm
  • Familial Dystonia, Idiopathic
  • CIMDAG syndrome
  • Idiopathic (torsion) dystonia NOS
  • Tyrosine hydroxylase deficient dopa responsive dystonia
  • X-linked intellectual deficit-dystonia-dysarthria syndrome
  • Familial torsion dystonia
  • Hypermanganesemia with dystonia, polycythemia, and cirrhosis
  • Primary torsion dystonia
  • Torsion Spasm, Progressive
  • Spasm, Progressive Torsion
  • Hereditary progressive dystonia with marked diurnal fluctuation
  • Torsion dystonia parkinsonism Filipino type
  • Familial manganese-induced neurotoxicity
  • HMNDYT - hypermanganesemia with dystonia
  • Torsion dystonia (disorder)
  • CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome
  • Dystonia aphonia syndrome
  • Lubag
  • Generalised dystonia
  • Tyrosine hydroxylase deficiency
  • Dystonia 6
  • THAP1 dystonia
  • Dystonias, Idiopathic Familial
  • X-linked torsion dystonia parkinsonism syndrome
  • Disorder of manganese metabolism
  • Idiopathic familial dystonia (disorder)
  • Idiopathic Familial Dystonias
  • Segawa dystonia
  • Adult-onset familial idiopathic dystonia
  • Autosomal dominant idiopathic familial dystonia
  • Generalized dystonia
  • Autosomal recessive dopa responsive dystonia
  • Partington-Mulley syndrome
  • TORSION DIS CHILDHOOD
  • Schwalbe disease
  • Dystonia Deformans Musculorum
  • Adult-onset familial primary dystonia
  • Autosomal dominant Segawa syndrome
  • Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
  • Primary dystonia DYT17 type
  • X-linked dystonia parkinsonism
  • Dystonia, Idiopathic Familial
  • Partington X-linked intellectual disability syndrome
  • Partington x-linked mental retardation syndrome
  • Childhood Torsion Disease
  • Diurnal dystonia
  • Idiopathic Torsion Dystonias
  • Familial Dystonias, Idiopathic
  • Dystonias, Torsion
  • Partington syndrome
  • Primary dystonia type 4
  • Dopa responsive dystonia
  • Mohr-Tranebjaerg syndrome
  • Autosomal recessive Segawa syndrome
  • Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome
  • Ziehen Oppenheim disease
Frequently Asked Questions
What is the ICD-10 code for genetic torsion dystonia?

The ICD-10-CM code for genetic torsion dystonia is G24.1. The full clinical description is "Genetic torsion dystonia". G24.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G24.1 mean?

ICD-10-CM code G24.1 represents “Genetic torsion 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 G24.1 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.

How does G24.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like genetic torsion 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 G24.1?

G24.1 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.