Q25.1 ICD-10-CM Code: Coarctation of aorta
Compare with another code for Q25.1Check this code on a claim
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 2 inclusion terms
Billable · FY2027A valid, specific ICD-10-CM code, reportable for dates of service in FY2027.
What you need to know
Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too, and is marked with where it comes from.
- IncludesWhat this code covers
- Coarctation of aorta (preductal) (postductal)
- Stenosis of aorta
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 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 Q25.1 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
Inclusion Terms
Alternative terms the tabular list files under this code.
- Coarctation of aorta (preductal) (postductal)
- Stenosis of aorta
Coding context
Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.
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.
Verify Before Coding
- CC as a secondary diagnosis (FY2027). 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-derived relationships — computed from published CMS and AHRQ datasets
Other codes that name Q25.1 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 Excludes2 note: P29 — Cardiovascular disorders originating in the perinatal period (via Q25.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 2 Code Also instructions across 2 chapters: I27.21 — Secondary pulmonary arterial hypertension (via Q25.-), Z71.87 — Encounter for pediatric-to-adult transition counseling (via Q25.-).
These codes suggest coding this condition alongside when both are present.
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 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 45 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, Q25.21 — Interruption of aortic arch, Q25.29 — Other atresia of aorta, Q25.3 — Supravalvular aortic stenosis, 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, Q87.3 — Congenital malformation syndromes involving early overgrowth, Q87.5 — Other congenital malformation syndromes with other skeletal changes, Q87.81 — Alport syndrome, Q87.82 — Arterial tortuosity syndrome, Q87.83 — Bardet-Biedl syndrome, Q87.84 — Laurence-Moon syndrome, Q87.85 — MED13L syndrome, Q87.86 — Kleefstra syndrome, +24 more
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Cardiac and circulatory congenital anomalies).
Q24.0 — Dextrocardia, 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, Q25.2 — Atresia of aorta, Q25.21 — Interruption of aortic arch, Q25.29 — Other atresia of aorta, Q25.3 — Supravalvular aortic stenosis, Q25.4 — Other congenital malformations of aorta, Q25.40 — Congenital malformation of aorta unspecified, Q25.41 — Absence and aplasia of aorta, Q25.42 — Hypoplasia of aorta, Q25.43 — Congenital aneurysm of aorta, Q25.44 — Congenital dilation 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 “Stricture”, “Malformation”, “Anomaly, anomalous”, …; these codes share that main term but sit in a different category of the Tabular List.
Q23.3 — Congenital mitral insufficiency (mitral, insufficiency), Q23.81 — Bicuspid aortic valve (heart, valve NEC, aortic, bicuspid valve), Q23.82 — Congenital mitral valve cleft leaflet (mitral, cleft), Q23.88 — Other congenital malformations of aortic and mitral valves (mitral valve, specified NEC), Q23.9 — Congenital malformation of aortic and mitral valves, unspecified (aortic valve), Q24.3 — Pulmonary infundibular stenosis (infundibulum cardia), Q24.4 — Congenital subaortic stenosis (subaortic), Q24.5 — Malformation of coronary vessels (coronary vessels), Q24.8 — Other specified congenital malformations of heart (myocardium), Q24.9 — Congenital malformation of heart, unspecified (heart), Q26.0 — Congenital stenosis of vena cava (vena cava NEC, congenital), Q26.1 — Persistent left superior vena cava (great, vein, persistent left superior vena cava), Q26.2 — Total anomalous pulmonary venous connection (pulmonary, venous connection, total), Q26.3 — Partial anomalous pulmonary venous connection (pulmonary, venous connection, partial), Q26.4 — Anomalous pulmonary venous connection, unspecified (opening, pulmonary veins), Q26.5 — Anomalous portal venous connection (portal vein), Q26.6 — Portal vein-hepatic artery fistula (great, vein, portal vein-hepatic artery fistula), Q26.8 — Other congenital malformations of great veins (venous return), Q26.9 — Congenital malformation of great vein, unspecified (great, vein), Q27.0 — Congenital absence and hypoplasia of umbilical artery (umbilical artery), +519 more
Contextual Map
Every relationship of Q25.1 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 Q25.1 with these 3 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-fy2027
- Q20-Q28 — Congenital malformations of the circulatory system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes2 notes
- P29 — Cardiovascular disorders originating in the perinatal period[Excludes2](via Q25.-): “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code Also instructions
- I27.21 — Secondary pulmonary arterial hypertension[Code Also](via Q25.-): “congenital heart disease (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Z71.87 — Encounter for pediatric-to-adult transition counseling[Code Also](via Q25.-): “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
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) · FY2027
- 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) · FY2027
- 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) · FY2027
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. 15,708 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Anomaly, anomalous (congenital) (unspecified type), aorta NEC (arch), coarctation (preductal) (postductal)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Coarctation, aorta (preductal) (postductal)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Malformation (congenital), aorta, coarctation (preductal) (postductal)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Malformation (congenital), aorta, stenosis[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Stenosis, stenotic (cicatricial), aorta (ascending) (supraventricular) (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Stricture, aorta (ascending) (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes (25)
- Q25 — Congenital malformations of great arteries[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.0 — Patent ductus arteriosus[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.2 — Atresia of aorta[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.21 — Interruption of aortic arch[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.29 — Other atresia of aorta[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.3 — Supravalvular aortic stenosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.4 — Other congenital malformations of aorta[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q25.40 — Congenital malformation of aorta unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 17 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Reference
Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.
Indexed Clinical Terms (6)
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.
- Anomaly, anomalous (congenital) (unspecified type), aorta NEC (arch), coarctation (preductal) (postductal)
- Coarctation, aorta (preductal) (postductal)
- Malformation (congenital), aorta, coarctation (preductal) (postductal)
- Malformation (congenital), aorta, stenosis
- Stenosis, stenotic (cicatricial), aorta (ascending) (supraventricular) (congenital)
- Stricture, aorta (ascending) (congenital)
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-derived 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 editorial 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.
Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources
Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules
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. "Q25.1 — Coarctation of aorta." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q25.1-coarctation-of-aorta
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionCoarctation of aorta
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 Q25.1 in its code family, with their registry titles.
- Q25 — Congenital malformations of great arteries
- Q25.0 — Patent ductus arteriosus
- Q25.2 — Atresia of aorta
- Q25.21 — Interruption of aortic arch
- Q25.29 — Other atresia of aorta
- Q25.3 — Supravalvular aortic stenosis
- Q25.4 — Other congenital malformations of aorta
- Q25.40 — Congenital malformation of aorta unspecified
- Q25.41 — Absence and aplasia of aorta
- Q25.42 — Hypoplasia of aorta