Q21 ICD-10-CM Code: Congenital malformations of cardiac septa
Compare with another codeCheck this code on a claim
Billing Status: NO. This is a non-billable ICD-10-CM code: report a more specific billable code beneath it.
Coding at a Glance
- Tabular directives
- 1 Excludes1
Category · FY2027A non-billable heading in the tabular list: report a more specific code beneath it.
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; the Instructions section marks which is which.
- Excludes1Never report with this code
- acquired cardiac septal defect (I51.0)
Most relevant related codes MedCoder-derived
- Q21.0Ventricular septal defectMore specific code
- Q21.1Atrial septal defectMore specific code
- Q21.10Atrial septal defect, unspecifiedMore specific code
- Q21.11Secundum atrial septal defectMore specific code
- Q21.12Patent foramen ovaleMore specific code
- Q21.13Coronary sinus atrial septal defectMore specific code
Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for Q21 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
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).
- acquired cardiac septal defect (I51.0) Compare Q21 vs I51.0 →
Coder workflow for Q21
MedCoder structured workflow — derived from this code’s own official record
Before you code Q21
- Q21 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
ReviewQ21.0, Q21.1, Q21.2, Q21.3, Q21.4, Q21.8, Q21.9
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q21. 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 one of the more specific codes beneath Q21?
Yes → Select that code and continue the checks below on its own page.
No → Q21 cannot be reported as written; query for the specificity its subcategory needs. - Does the documentation support a condition named in Q21’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.ReviewI51.0
Consider Q21. 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 Q21(1 note)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q21: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareI51.0
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 Q21 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).
ReviewI51.0
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.
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
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 Q21 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.
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.
These codes instruct coders to additionally report this code when it applies.
Referenced by 3 Code Also instructions across 3 chapters: I27.21 — Secondary pulmonary arterial hypertension, Q87.85 — MED13L syndrome, Z71.87 — Encounter for pediatric-to-adult transition counseling.
These codes suggest coding this condition alongside when both are present.
Contextual Map
Every relationship of Q21 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 Q21 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-fy2027
- Q20-Q28 — Congenital malformations of the circulatory system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Excludes1
- I51.0 — Cardiac septal defect, acquired[Excludes1]: “acquired cardiac septal defect (I51.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes2 notes
- P29 — Cardiovascular disorders originating in the perinatal period[Excludes2]: “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Use Additional Code instructions
- Q87.88 — CTNNB1 syndrome[Use Additional Code]: “congenital heart malformations (Q20.0-Q24.9)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code Also instructions
- I27.21 — Secondary pulmonary arterial hypertension[Code Also]: “congenital heart disease (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q87.85 — MED13L syndrome[Code Also]: “congenital malformations of cardiac septa (Q21.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Z71.87 — Encounter for pediatric-to-adult transition counseling[Code Also]: “congenital malformations of the circulatory system (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Nearest codes (19)
- Q21.0 — Ventricular septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.1 — Atrial septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.10 — Atrial septal defect, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.11 — Secundum atrial septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.12 — Patent foramen ovale[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.13 — Coronary sinus atrial septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.14 — Superior sinus venosus atrial septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q21.15 — Inferior sinus venosus atrial septal defect[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 11 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.
Common coding questions
MedCoder editorial
Can Q21 be billed directly?
No. Q21 (Congenital malformations of cardiac septa) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
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
- 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. "Q21 — Congenital malformations of cardiac septa." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q21-congenital-malformations-of-cardiac-septa
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionCongenital malformations of cardiac septa
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 Q21 in its code family, with their registry titles.
- Q21.0 — Ventricular septal defect
- Q21.1 — Atrial septal defect
- Q21.10 — Atrial septal defect, unspecified
- Q21.11 — Secundum atrial septal defect
- Q21.12 — Patent foramen ovale
- Q21.13 — Coronary sinus atrial septal defect
- Q21.14 — Superior sinus venosus atrial septal defect
- Q21.15 — Inferior sinus venosus atrial septal defect
- Q21.16 — Sinus venosus atrial septal defect, unspecified
- Q21.19 — Other specified atrial septal defect
- Q21.2 — Atrioventricular septal defect
- Q21.20 — Atrioventricular septal defect, unspecified as to partial or complete
- Q21.21 — Partial atrioventricular septal defect
- Q21.22 — Transitional atrioventricular septal defect
- Q21.23 — Complete atrioventricular septal defect
- Q21.3 — Tetralogy of Fallot
- Q21.4 — Aortopulmonary septal defect
- Q21.8 — Other congenital malformations of cardiac septa
- Q21.9 — Congenital malformation of cardiac septum, unspecified