Q22.6 — Hypoplastic right heart syndrome
Is Q22.6 billable?
Yes — Q22.6 is billable for FY2027. Q22.6 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. Q22.6 may be submitted for encounters from October 1, 2026 through September 30, 2027.
Q22.6 at a glance
| Code | Q22.6 |
|---|---|
| Description | Hypoplastic right heart syndrome |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does Q22.6 group to?
Q22.6 sits in MDC 05 and helps define the logic of 2 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 306Cardiac Congenital and Valvular Disorders with MCCmedical
- 307Cardiac Congenital and Valvular Disorders without MCCmedical
As a secondary diagnosis, Q22.6 is a major complication or comorbidity (MCC), which can move a stay into a higher-paying DRG.
How is Q22.6 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to Q22.6. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Hypoplasia, hypoplastic › right heart syndrome
- Anomaly, anomalous › heart › obstructive NEC (congenital) (unspecified type)
- Syndrome › right › heart, hypoplastic
Excludes2 — not included here — inherited from Chapter 17
The conditions below are not part of Q22.6, but a patient may have both at the same time. When documentation supports it, Q22.6 and the excluded code may both be reported.
- inborn errors of metabolism (E70-E88)
How long has Q22.6 existed?
Q22.6 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.
What other codes are in the Q22 family? (8)
- Q22.0Pulmonary valve atresia
- Q22.1Congenital pulmonary valve stenosis
- Q22.2Congenital pulmonary valve insufficiency
- Q22.3Other congenital malformations of pulmonary valve
- Q22.4Congenital tricuspid stenosis
- Q22.5Ebstein's anomaly
- Q22.8Other congenital malformations of tricuspid valve
- Q22.9Congenital malformation of tricuspid valve, unspecified