G24.1 ICD-10-CM Code: Genetic torsion dystonia
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 7 inclusion terms · 1 Excludes2
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.
- MS-DRG 056 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC (MDC 01)
- MS-DRG 057 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC (MDC 01)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for G24.1 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on G24.1 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- dyskinesia
Source: inherited from G24
Inclusion Terms
Alternative terms the tabular list files under this code.
- Dystonia deformans progressiva
- Dystonia musculorum deformans
- Familial torsion dystonia
- Idiopathic familial dystonia
- Idiopathic (torsion) dystonia NOS
- (Schwalbe-) Ziehen-Oppenheim disease
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- athetoid cerebral palsy (G80.3) Compare G24.1 vs G80.3 →
Source: inherited from G24
Coder workflow for G24.1
MedCoder structured workflow — derived from this code’s own official record
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes2 — not part of G24.1(1 note)
Coding workflow: The conditions named in this note are not included in G24.1. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareG80.3
See the official tabular notes · Guidelines I.A.12.b
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Indexed Clinical Terms (13)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
- Disease, diseased, Schwalbe-Ziehen-Oppenheim
- Dysbasia, lordotica (progressiva)
- Dystonia, deformans progressiva
- Dystonia, familial
- Dystonia, idiopathic
- Dystonia, idiopathic, familial
- Dystonia, musculorum deformans
- Dystonia, torsion (familial) (idiopathic)
- Dystonia, torsion (familial) (idiopathic), genetic
- Schwalbe-Ziehen-Oppenheim disease
- Spasm, spastic, spasticity (s), torsion (progressive)
- Tortipelvis
- Ziehen-Oppenheim disease
Verify Before Coding
- No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name G24.1 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 1 Excludes1 note: R25 — Abnormal involuntary movements (via G24.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 1 Excludes2 note: F98.4 — Stereotyped movement disorders (via G24.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.
Named in the grouper logic of 2 MS-DRGs: DRG 056 (MDC 01), DRG 057 (MDC 01).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):NVS006 — Other nervous system disorders (often hereditary or degenerative) (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other nervous system disorders (often hereditary or degenerative)).
G21.9 — Secondary parkinsonism, unspecified, G23.0 — Hallervorden-Spatz disease, G23.1 — Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski], G23.2 — Striatonigral degeneration, G23.3 — Hypomyelination with atrophy of the basal ganglia and cerebellum, G23.8 — Other specified degenerative diseases of basal ganglia, G23.9 — Degenerative disease of basal ganglia, unspecified, G24.01 — Drug induced subacute dyskinesia, G24.02 — Drug induced acute dystonia, G24.09 — Other drug induced dystonia, G24.2 — Idiopathic nonfamilial dystonia, G24.3 — Spasmodic torticollis, G24.4 — Idiopathic orofacial dystonia, G24.5 — Blepharospasm, G24.8 — Other dystonia, G24.9 — Dystonia, unspecified, G25.0 — Essential tremor, G25.1 — Drug-induced tremor, G25.2 — Other specified forms of tremor, G25.3 — Myoclonus, +83 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Spasm, spastic, spasticity”, “Dysbasia”; these codes share that main term but sit in a different category of the Tabular List.
B33.0 — Epidemic myalgia (diaphragm, epidemic), F44.4 — Conversion disorder with motor symptom or deficit (hysterical), F45.8 — Other somatoform disorders (nervous), F48.8 — Other specified nonpsychotic mental disorders (occupational), F52.5 — Vaginismus not due to a substance or known physiological condition (vagina, psychogenic), F95.0 — Transient tic disorder (tic, transient of childhood), F95.1 — Chronic motor or vocal tic disorder (tic, chronic), F95.9 — Tic disorder, unspecified (tic), F98.4 — Stereotyped movement disorders (nodding), G45.9 — Transient cerebral ischemic attack, unspecified (cerebral), G50.0 — Trigeminal neuralgia (nerve, trigeminal), G51.3 — Clonic hemifacial spasm (Bell's), H51.8 — Other specified disorders of binocular movement (conjugate), H52.53 — Spasm of accommodation (of accommodation), I20.1 — Angina pectoris with documented spasm (heart), I73.9 — Peripheral vascular disease, unspecified (artery), I87.8 — Other specified disorders of veins (vein NEC), J38.5 — Laryngeal spasm (glottis), J39.2 — Other diseases of pharynx (throat), J98.01 — Acute bronchospasm (bronchus, bronchiole), +25 more
Contextual Map
Every relationship of G24.1 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run G24.1 with these 2 related codes in Claim Check
Hierarchy
- G00-G99 — Chapter 6: Diseases of the Nervous System (G00-G99) (G00-G99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G20-G26 — Extrapyramidal and movement disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes
- R25 — Abnormal involuntary movements[Excludes1](via G24.-): “specific movement disorders (G20-G26)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes
- F98.4 — Stereotyped movement disorders[Excludes2](via G24.-): “movement disorders of organic origin (G20-G25)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- NVS006 — Other nervous system disorders (often hereditary or degenerative)[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 056 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC[MS-DRG]: “DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 057 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC[MS-DRG]: “DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
MDC crossing
- MDC 01 — Diseases and Disorders of the Nervous System[MDC crossing]: “Diseases and Disorders of the Nervous System — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 8,919 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries (13)
- Disease, diseased, Schwalbe-Ziehen-Oppenheim[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dysbasia, lordotica (progressiva)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, deformans progressiva[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, familial[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, idiopathic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, idiopathic, familial[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, musculorum deformans[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dystonia, torsion (familial) (idiopathic)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- and 5 more
Nearest codes (11)
- G24 — Dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.0 — Drug induced dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.01 — Drug induced subacute dyskinesia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.02 — Drug induced acute dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.09 — Other drug induced dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.2 — Idiopathic nonfamilial dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.3 — Spasmodic torticollis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G24.4 — Idiopathic orofacial dystonia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 3 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "G24.1 — Genetic torsion dystonia." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/g24.1-genetic-torsion-dystonia
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionGenetic torsion dystonia
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to G24.1 in its code family, with their registry titles.
- G24 — Dystonia
- G24.0 — Drug induced dystonia
- G24.01 — Drug induced subacute dyskinesia
- G24.02 — Drug induced acute dystonia
- G24.09 — Other drug induced dystonia
- G24.2 — Idiopathic nonfamilial dystonia
- G24.3 — Spasmodic torticollis
- G24.4 — Idiopathic orofacial dystonia
- G24.5 — Blepharospasm
- G24.8 — Other dystonia