Q21.22 ICD-10-CM Code: Transitional atrioventricular septal defect
Compare with another codeCheck 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
- 6 inclusion terms · 1 Excludes1
- Risk adjustment
- RxHCC V08 category 191
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; the Instructions section marks which is which.
- Excludes1Never report with this code
- acquired cardiac septal defect (I51.0)
- IncludesWhat this code covers
- Intermediate atrioventricular canal
- Intermediate atrioventricular septal defect
- Intermediate endocardial cushion defect
- Ostium primum atrial septal defect (type I) with separate atrioventricular valves and a small or restrictive inlet VSD
Most relevant related codes MedCoder-derived
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.
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 Q21.22 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 Q21.22 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Intermediate atrioventricular canal
- Intermediate atrioventricular septal defect
- Intermediate endocardial cushion defect
- Ostium primum atrial septal defect (type I) with separate atrioventricular valves and a small or restrictive inlet VSD
- Transitional atrioventricular canal
- Transitional endocardial cushion defect
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 Q21.22 vs I51.0 →
Source: inherited from Q21
Coder workflow for Q21.22
MedCoder structured workflow — derived from this code’s own official record
Before you code Q21.22
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q21.22. 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 Q21.22’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 Q21.22. 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 Q21.22(1 note)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q21.22: 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 Q21.22 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
- 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 Q21.22 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 Q21.-).
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 Q21.-).
These codes instruct coders to additionally report this code when it applies.
Referenced by 4 Code Also instructions across 3 chapters: I27.21 — Secondary pulmonary arterial hypertension (via Q21.-), Q87.85 — MED13L syndrome (via Q21.-), Q90 — Down syndrome (via Q21.2.-), Z71.87 — Encounter for pediatric-to-adult transition counseling (via Q21.-).
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 60 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.
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, Q21.20 — Atrioventricular septal defect, unspecified as to partial or complete, Q21.21 — Partial 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, 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, Q24.8 — Other specified congenital malformations of heart, +39 more
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Cardiac and circulatory congenital anomalies).
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, Q21.23 — 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, Q22.0 — Pulmonary valve atresia, Q22.1 — Congenital pulmonary valve stenosis, Q22.2 — Congenital pulmonary valve insufficiency, Q22.3 — Other congenital malformations of pulmonary valve, Q22.4 — Congenital tricuspid stenosis, +87 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Defect, defective”; these codes share that main term but sit in a different category of the Tabular List.
M89.9 — Disorder of bone, unspecified (osseous, major, multiple sites), M95.8 — Other specified acquired deformities of musculoskeletal system (osteochondral NEC), O08.1 — Delayed or excessive hemorrhage following ectopic and molar pregnancy (coagulation, with, molar pregnancy), O67.0 — Intrapartum hemorrhage with coagulation defect (coagulation, intrapartum), O72.3 — Postpartum coagulation defects (coagulation, postpartum, with hemorrhage), O99.13 — Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating the puerperium (coagulation, postpartum), P61.6 — Other transient neonatal disorders of coagulation (coagulation, newborn, transient), Q06.3 — Other congenital cauda equina malformations (developmental, cauda equina), Q13.89 — Other congenital malformations of anterior segment of eye (Descemet's membrane, congenital), Q20.1 — Double outlet right ventricle (Taussig-Bing), Q27.9 — Congenital malformation of peripheral vascular system, unspecified (vascular, congenital), Q28.9 — Congenital malformation of circulatory system, unspecified (circulation, newborn), Q34.9 — Congenital malformation of respiratory system, unspecified (respiratory system, congenital), Q39.9 — Congenital malformation of esophagus, unspecified (esophagus, congenital), Q62.2 — Congenital megaureter (obstructive, congenital, ureter, megaureter), Q62.31 — Congenital ureterocele, orthotopic (obstructive, congenital, ureter, orthotopic ureterocele), Q62.32 — Cecoureterocele (obstructive, congenital, ureter, cecoureterocele), Q62.39 — Other obstructive defects of renal pelvis and ureter (renal pelvis, obstructive), Q63.8 — Other specified congenital malformations of kidney (renal pelvis), Q71.4 — Longitudinal reduction defect of radius (reduction, limb, upper, longitudinal, radius), +85 more
Contextual Map
Every relationship of Q21.22 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 Q21.22 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
Referenced by Excludes2 notes
- P29 — Cardiovascular disorders originating in the perinatal period[Excludes2](via Q21.-): “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](via Q21.-): “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](via Q21.-): “congenital heart disease (Q20-Q28)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q87.85 — MED13L syndrome[Code Also](via Q21.-): “congenital malformations of cardiac septa (Q21.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q90 — Down syndrome[Code Also](via Q21.2.-): “associated physical condition(s), such as atrioventricular septal defect (Q21.2-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Z71.87 — Encounter for pediatric-to-adult transition counseling[Code Also](via Q21.-): “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
- Canal, atrioventricular, intermediate[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Canal, atrioventricular, transitional[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Defect, defective, atrial septal, ostium primum type (type I), with, separate atrioventricular valves, and small or restrictive inlet VSD[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Defect, defective, atrioventricular, septal, intermediate[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Defect, defective, atrioventricular, septal, transitional[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Defect, defective, cushion, endocardial, intermediate[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Defect, defective, cushion, endocardial, transitional[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes (19)
- Q21 — Congenital malformations of cardiac septa[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- 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
- and 11 more
Change history
- FY2023 — Added to the code set[Change history]— CMS release files (code change ledger) · icd10cm-fy2023
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 (7)
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.
- Canal, atrioventricular, intermediate
- Canal, atrioventricular, transitional
- Defect, defective, atrial septal, ostium primum type (type I), with, separate atrioventricular valves, and small or restrictive inlet VSD
- Defect, defective, atrioventricular, septal, intermediate
- Defect, defective, atrioventricular, septal, transitional
- Defect, defective, cushion, endocardial, intermediate
- Defect, defective, cushion, endocardial, transitional
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 20, 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. "Q21.22 — Transitional atrioventricular septal defect." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q21.22-transitional-atrioventricular-septal-defect
Change history
- FY2023 — October 1, 2022Added to the code setTransitional atrioventricular septal defectFY2023 changes
Nearest Codes in This Family
Official ICD-10-CM classifications closest to Q21.22 in its code family, with their registry titles.
- 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
- Q21.23 — 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