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Q21.0 ICD-10-CM Code: Ventricular septal defect

ICD-10-CM Code View

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FY 2026 Apr update / Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0) / Congenital malformations of the circulatory system (Q20-Q28)

Q21.0

Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidance

Ventricular septal defect

A hole in the wall separating the two lower chambers of the heart, allowing blood to flow abnormally between them.

Buddy the Bee presenting code insight

Buddy Insight

Ventricular septal defect is the most common congenital heart defect, involving a hole in the wall between the heart's lower chambers.

CMS-HCC V28

N/A

Not mapped

CMS-HCC V24

N/A

Not mapped

ACA/HHS

HCC 139

Varies by metal level

ESRD/PACE

N/A

Not mapped

RXHCC

HCC 191

RAF 0.150

Code Book Path

Official
Q21Congenital malformations of cardiac septa
Q21.0Ventricular septal defect

Inclusion Terms

Official
  • Roger's disease

Excludes 2

Official

ICD-10-CM does not list Excludes 2 notes for Q21.0 in this effective period.

Related Child Codes

Official
Q21.1Atrial septal defect
Q21.2Atrioventricular septal defect
Q21.3Tetralogy of Fallot
Q21.4Aortopulmonary septal defect
Q21.8Other congenital malformations of cardiac septa

Includes

Official

ICD-10-CM does not list Includes notes for Q21.0 in this effective period.

Excludes 1

Official
  • acquired cardiac septal defect (I51.0)

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for Q21.0 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for Q21.0 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for Q21.0 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Echocardiographic confirmation of ventricular septal defect
Size and location of the defect
Hemodynamic significance and shunt direction
Associated cardiac anomalies

MEAT Support

HCC Buddy guidance
Echocardiographic confirmation of ventricular septal defect
Size and location of the defect
Hemodynamic significance and shunt direction
Associated cardiac anomalies

Audit Caution

HCC Buddy guidance
Confusing with atrial septal defects
Using post-surgical codes when defect remains open
Missing associated cardiac anomalies
Not documenting hemodynamic significance

Common Mistakes

HCC Buddy guidance
Q21.1 — atrial septal defect
Q21.2 — atrioventricular septal defect
Z95.89 — presence of other cardiac implants (post-surgical)
I25.2 — old myocardial infarction

Last updated: FY2026 ICD-10-CM Apr update, Apr 1, 2026 through Sep 30, 2026. CMS-HCC V28 is 100% phased in for payment year 2026.

Is Q21.0 an HCC code?

Q21.0 is not in the CMS-HCC V28 or V24 community payment model, but it does map to Congenital Heart/Circulatory Disorders and Fontan Circulation under the Part D RxHCC model.

Code
Q21.0
Description
Ventricular septal defect
HCC (V28)
No CMS-HCC V28 mapping
RAF
Billable
Yes
Payment year
2026

HCC Category Mapping

RxHCCHCC 191, Congenital Heart/Circulatory Disorders and Fontan Circulation
0.150

Each model's RAF is its CMS base weight for that model's standard population, so weights are not directly comparable across models: CMS-HCC V28 and V24 use Community, Non-Dual, Aged; ESRD uses the dialysis continuing-enrollee model; RxHCC is the Part D continuing-enrollee, non-low-income, aged weight (a larger scale than CMS-HCC). ACA/HHS has no single weight — it varies by metal level. Actual per-patient RAF contribution depends on member segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.

Work Q21.0 in the Code Book — tabular path, V28 RAF, and MEAT checklist →

MEAT Criteria for Q21.0

For Q21.0to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically, it has to be re-documented and supported each calendar year.

  • MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
  • EEvaluate: test results, medication response, or physical findings reviewed by the provider
  • AAssess: explicit mention in the assessment or plan with acknowledgment of status
  • TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis

Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed Q21.0 during that encounter, not just copy-forwarded from a problem list.

Coder workflow notes

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What This Code Means

Q21.0 is the ICD-10-CM diagnosis code for ventricular septal defect. A hole in the wall separating the two lower chambers of the heart, allowing blood to flow abnormally between them. Q21.0 sits in the ICD-10-CM chapter for congenital malformations, deformations and chromosomal abnormalities (q00-qa0), within the section covering congenital malformations of the circulatory system (q20-q28).

Q21.0 is a billable ICD-10-CM code but does not map to a payment HCC under the CMS-HCC V28, V24, ESRD, or RxHCC risk adjustment models. It can be reported on Medicare Advantage encounter data submissions but it does not contribute to a beneficiary's RAF score and therefore does not affect risk-adjusted payments to the plan.

This code does not map to a CMS-HCC V28 payment category. Capture depends on documentation that supports the diagnosis; verify the HCC assignment against the current CMS mapping for the applicable payment year. Coders reviewing Q21.0 should check whether additional documentation would support a more specific child code in the same hierarchy that does map to a payment HCC, capturing the correct specificity is the highest-impact RAF improvement available within accurate coding.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for Q21.0 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Document the size and location of the defect (muscular, membranous, inlet, outlet) when available for more specific coding if needed
  • Note whether the defect is isolated or associated with other cardiac anomalies, as this affects clinical management and coding

Clinical Significance

Ventricular septal defect is the most common congenital heart defect, involving a hole in the wall between the heart's lower chambers. While small defects may close spontaneously, larger defects can lead to heart failure and require surgical intervention to prevent long-term complications.

Documentation Requirements

  • Echocardiographic confirmation of ventricular septal defect
  • Size and location of the defect
  • Hemodynamic significance and shunt direction
  • Associated cardiac anomalies
  • Signs of heart failure or pulmonary hypertension
  • Surgical closure history if performed
  • Current cardiac function and exercise tolerance
  • Growth and development assessment in children

Commonly Confused Codes

  • Q21.1: atrial septal defect
  • Q21.2: atrioventricular septal defect
  • Z95.89: presence of other cardiac implants (post-surgical)
  • I25.2: old myocardial infarction
  • Q22.1: congenital pulmonary valve stenosis

Child Codes

Code Hierarchy

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