Q24.0 ICD-10-CM Code: Dextrocardia
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 4 Excludes1
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 v43, Appendix B.
- MS-DRG 306 — CARDIAC CONGENITAL AND VALVULAR DISORDERS WITH MCC (MDC 05)
- MS-DRG 307 — CARDIAC CONGENITAL AND VALVULAR DISORDERS WITHOUT MCC (MDC 05)
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 Q24.0 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on Q24.0 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- dextrocardia with situs inversus (Q89.3) Compare Q24.0 vs Q89.3 →
- isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6) Compare Q24.0 vs Q20.6 →
- mirror-image atrial arrangement with situs inversus (Q89.3) Compare Q24.0 vs Q89.3 →
- endocardial fibroelastosis (I42.4) inherited from Q24Compare Q24.0 vs I42.4 →
Coder workflow for Q24.0
MedCoder structured workflow — derived from this code’s own official record
Before you code Q24.0
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q24.0. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support a condition named in Q24.0’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider Q24.0. Then confirm the code is valid for the date of service in the Verify section.
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
Excludes1 — check before selecting Q24.0(4 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q24.0: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
See the official tabular notes · Guidelines I.A.12.a
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition Q24.0 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
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 (3)
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.
Verify Before Coding
- CC as a secondary diagnosis (FY2026). Can raise the stay's MS-DRG severity tier.
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 Q24.0 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: Q89.3 — Situs inversus.
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: P29 — Cardiovascular disorders originating in the perinatal period (via Q24.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 1 Use Additional Code instruction: Q87.88 — CTNNB1 syndrome (via Q24.-).
These codes instruct coders to additionally report this code when it applies.
Referenced by 2 Code Also instructions across 2 chapters: I27.21 — Secondary pulmonary arterial hypertension (via Q24.-), Z71.87 — Encounter for pediatric-to-adult transition counseling (via Q24.-).
These codes suggest coding this condition alongside when both are present.
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 52 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 2 MS-DRGs: DRG 306 (MDC 05), DRG 307 (MDC 05).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL001 — Cardiac and circulatory congenital anomalies (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 process (MS-DRG)
Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.
E78.71 — Barth syndrome, E78.72 — Smith-Lemli-Opitz syndrome, Q20.9 — Congenital malformation of cardiac chambers and connections, unspecified, Q23.81 — Bicuspid aortic valve, Q23.82 — Congenital mitral valve cleft leaflet, Q23.88 — Other congenital malformations of aortic and mitral valves, Q23.9 — Congenital malformation of aortic and mitral valves, unspecified, Q24.1 — Levocardia, Q24.2 — Cor triatriatum, Q24.3 — Pulmonary infundibular stenosis, Q24.4 — Congenital subaortic stenosis, Q24.8 — Other specified congenital malformations of heart, Q24.9 — Congenital malformation of heart, unspecified, Q27.30 — Arteriovenous malformation, site unspecified, Q27.4 — Congenital phlebectasia, Q28.0 — Arteriovenous malformation of precerebral vessels, Q28.1 — Other malformations of precerebral vessels, Q28.8 — Other specified congenital malformations of circulatory system, Q28.9 — Congenital malformation of circulatory system, unspecified, Q87.2 — Congenital malformation syndromes predominantly involving limbs, +31 more
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Cardiac and circulatory congenital anomalies).
Q23.0 — Congenital stenosis of aortic valve, Q23.1 — Congenital insufficiency of aortic valve, Q23.2 — Congenital mitral stenosis, Q23.3 — Congenital mitral insufficiency, Q23.4 — Hypoplastic left heart syndrome, Q23.8 — Other congenital malformations of aortic and mitral valves, Q23.81 — Bicuspid aortic valve, Q23.82 — Congenital mitral valve cleft leaflet, Q23.88 — Other congenital malformations of aortic and mitral valves, Q23.9 — Congenital malformation of aortic and mitral valves, unspecified, Q24.1 — Levocardia, Q24.2 — Cor triatriatum, Q24.3 — Pulmonary infundibular stenosis, Q24.4 — Congenital subaortic stenosis, Q24.5 — Malformation of coronary vessels, Q24.6 — Congenital heart block, Q24.8 — Other specified congenital malformations of heart, Q24.9 — Congenital malformation of heart, unspecified, Q25.0 — Patent ductus arteriosus, Q25.1 — Coarctation of aorta, +87 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Malposition”, “Transposition”; these codes share that main term but sit in a different category of the Tabular List.
Q15.8 — Other specified congenital malformations of eye (congenital, eye), Q16.3 — Congenital malformation of ear ossicles (congenital, ear, ossicles), Q16.9 — Congenital malformation of ear causing impairment of hearing, unspecified (congenital, auricle, causing impairment of hearing), Q17.4 — Misplaced ear (congenital, ear), Q17.8 — Other specified congenital malformations of ear (congenital, auditory canal), Q18.2 — Other branchial cleft malformations (congenital, auricle, cervical), Q18.8 — Other specified congenital malformations of face and neck (congenital, facial features), Q20.0 — Common arterial trunk (congenital, arterial trunk), Q20.3 — Discordant ventriculoarterial connection (aorta), Q20.5 — Discordant atrioventricular connection (corrected), Q25.49 — Other congenital malformations of aorta (congenital, aorta), Q25.79 — Other congenital malformations of pulmonary artery (congenital, artery, pulmonary), Q26.8 — Other congenital malformations of great veins (congenital, vena cava), Q27.8 — Other specified congenital malformations of peripheral vascular system (congenital, vein), Q30.8 — Other congenital malformations of nose (congenital, nose, nasal), Q31.8 — Other congenital malformations of larynx (congenital, larynx), Q32.1 — Other congenital malformations of trachea (congenital, trachea), Q32.4 — Other congenital malformations of bronchus (congenital, bronchus), Q33.8 — Other congenital malformations of lung (congenital, lung), Q34.8 — Other specified congenital malformations of respiratory system (congenital, respiratory organ or system NEC), +69 more
Lab tests where this diagnosis supports Medicare coverage (NCD)
Medicare's National Coverage Determination (NCD) program lists this diagnosis as medical justification for these lab tests.
Contextual Map
Every relationship of Q24.0 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 Q24.0 with these 6 related codes in Claim Check
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q20-Q28 — Congenital malformations of the circulatory system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes1
- Q20.6 — Isomerism of atrial appendages[Excludes1]: “isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- Q89.3 — Situs inversus[Excludes1]: “dextrocardia with situs inversus (Q89.3)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes1 notes
- Q89.3 — Situs inversus[Excludes1]: “dextrocardia NOS (Q24.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes
- P29 — Cardiovascular disorders originating in the perinatal period[Excludes2](via Q24.-): “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Use Additional Code instructions
- Q87.88 — CTNNB1 syndrome[Use Additional Code](via Q24.-): “congenital heart malformations (Q20.0-Q24.9)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Code Also instructions
- I27.21 — Secondary pulmonary arterial hypertension[Code Also](via Q24.-): “congenital heart disease (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- Z71.87 — Encounter for pediatric-to-adult transition counseling[Code Also](via Q24.-): “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- MAL001 — Cardiac and circulatory congenital anomalies[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2026
- DRG 306 — CARDIAC CONGENITAL AND VALVULAR DISORDERS WITH MCC[MS-DRG]: “CARDIAC CONGENITAL AND VALVULAR DISORDERS WITH MCC (MDC 05)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 307 — CARDIAC CONGENITAL AND VALVULAR DISORDERS WITHOUT MCC[MS-DRG]: “CARDIAC CONGENITAL AND VALVULAR DISORDERS WITHOUT MCC (MDC 05)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 05 — Diseases and Disorders of the Circulatory System[MDC crossing]: “Diseases and Disorders of the Circulatory 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. 17,209 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Dextrocardia (true)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Malposition, congenital, heart, dextrocardia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Transposition (congenital), heart[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes (9)
- Q24 — Other congenital malformations of heart[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.1 — Levocardia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.2 — Cor triatriatum[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.3 — Pulmonary infundibular stenosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.4 — Congenital subaortic stenosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.5 — Malformation of coronary vessels[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.6 — Congenital heart block[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q24.8 — Other specified congenital malformations of heart[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 1 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 FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 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 — v43 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. "Q24.0 — Dextrocardia." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q24.0-dextrocardia
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionDextrocardia
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), 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 Q24.0 in its code family, with their registry titles.
- Q24 — Other congenital malformations of heart
- Q24.1 — Levocardia
- Q24.2 — Cor triatriatum
- Q24.3 — Pulmonary infundibular stenosis
- Q24.4 — Congenital subaortic stenosis
- Q24.5 — Malformation of coronary vessels
- Q24.6 — Congenital heart block
- Q24.8 — Other specified congenital malformations of heart
- Q24.9 — Congenital malformation of heart, unspecified