2026 ICD-10-CM Diagnosis Code Q20.4Double inlet ventricle
ICD-10-CM Codes›Q00-Q99›Q20-Q28›Q20
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
Q20.4 is a billable ICD-10-CM diagnosis code for double inlet ventricle. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 306 through 307. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Cardiac and circulatory congenital anomalies.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q20.4 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Abnormality of left atrioventricular valve chordae tendinae
- Abnormality of left atrioventricular valve in double inlet ventricle
- Abnormality of right atrioventricular valve chordae tendinae
- Abnormality of right atrioventricular valve in double inlet ventricle
- Absent left atrioventricular valve leaflets
- Absent right atrioventricular valve leaflets
- Accessory tissue on left atrioventricular valve leaflet
- Arcade abnormality of left atrioventricular valve chordae
- Common atrioventricular orifice in double inlet ventricle
- Common ventricle
- Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle
- Congenital abnormality of left atrioventricular valve in double inlet ventricle
- Congenital abnormality of left atrioventricular valve papillary muscle
- Congenital abnormality of right atrioventricular valve chordae tendinae in double inlet ventricle
- Congenital abnormality of right atrioventricular valve in double inlet ventricle
- Congenital abnormality of right atrioventricular valve leaflet in double inlet ventricle
- Congenital abnormality of right atrioventricular valve papillary muscle
- Congenital abnormality of right atrioventricular valve papillary muscle in double inlet ventricle
- Congenital absence of left atrioventricular valve papillary muscle
- Congenital absence of papillary muscle
- Congenital anomaly of left-sided atrioventricular valve in double inlet ventricle
- Congenital anomaly of right-sided atrioventricular valve in double inlet ventricle
- Congenital cleft of cardiac valve
- Congenital fusion of left atrioventricular valve papillary muscles
- Congenital hypoplastic left atrioventricular valve papillary muscle
- Congenital parachute malformation of left atrioventricular valve
- Congenital parachute malformation of right atrioventricular valve
- Double inlet left ventricle
- Double inlet right ventricle
- Double inlet to solitary ventricle of indeterminate morphology
- Double inlet to ventricle of indeterminate morphology
- Double inlet ventricle
- Double orifice of left atrioventricular valve
- Double orifice of right atrioventricular valve
- Double orifice of right atrioventricular valve in double inlet ventricle
- Ebstein's anomaly of left atrioventricular valve
- Ebstein's anomaly of left atrioventricular valve in functionally univentricular heart
- Functional single ventricle
- Functionally univentricular heart
- Hypoplasia of left atrioventricular valve annulus in double inlet ventricle
- Hypoplasia of right atrioventricular valve annulus in double inlet ventricle
- Left atrioventricular valve atresia
- Left atrioventricular valve chordae to outlet septum
- Left atrioventricular valve chordae too long
- Left atrioventricular valve chordae too short
- Left atrioventricular valve dysplasia
- Left atrioventricular valve hypoplasia
- Left atrioventricular valve leaflet abnormality
- Left atrioventricular valve leaflet dysplasia
- Left atrioventricular valve prolapse
- Left atrioventricular valve stenosis
- Left atrioventricular valve stenosis in double inlet ventricle
- Overriding left atrioventricular valve
- Overriding right atrioventricular valve
- Right atrioventricular valve dysplasia
- Right atrioventricular valve hypoplasia
- Right atrioventricular valve leaflets absent in double inlet ventricle
- Right atrioventricular valve stenosis
- Single left ventricle
- Single right ventricle
- Solitary ventricle of indeterminate morphology
- Straddling left atrioventricular valve
- Straddling right atrioventricular valve
- Straddling tricuspid valve
- True cleft of left atrioventricular valve leaflet
- Two atrioventricular valves in double inlet ventricle
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Common ventricle
- Cor triloculare biatriatum
- Single ventricle
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Absence (of) (organ or part) (complete or partial)
- septum
- ventricular (congenital) - Q20.4
- ventricular septum - Q20.4
- Agenesis
- septum
- ventricular - Q20.4
- Cor
- triloculare - Q20.8
- biatrium - Q20.4
- with rudimentary ventricle - Q20.4
- Double
- inlet ventricle - Q20.4
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Absence(of) (organ or part) (complete or partial)
- septum
- ventricular (congenital)
- Absence(of) (organ or part) (complete or partial)
- ventricular septum
- Agenesis
- septum
- ventricular
- Common
- ventricle
- Cor
- triloculare
- biatrium
- Displacement, displaced
- ventricular septum
- with rudimentary ventricle
- Double
- inlet ventricle
- Single
- ventricle
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Congenital Heart Defects
Congenital heart defects (CHDs) are problems with the structure of the heart. "Congenital" means that that the problems are present at birth. These defects happen when a fetus's heart doesn't develop normally during pregnancy. Congenital heart defects are the most common type of birth defect.
The full article covers:
- What are congenital heart defects?
- What causes congenital heart defects?
- Who is more likely to have a baby with a congenital heart defect?
- What are the symptoms of congenital heart defects?
- What other problems do congenital heart defects cause?
- How are congenital heart defects diagnosed?
- What are the treatments for congenital heart defects?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q20.4 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q20.4Overview
Is Q20.4 (Congenital malformations of cardiac chambers and connections) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report double inlet ventricle on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does Q20.4 group to?
When double inlet ventricle is the principal diagnosis on an inpatient stay, it groups to MS-DRG 306, 307, with relative weights from 0.9132 to 1.5758 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q20.4 exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for double inlet ventricle on inpatient claims.
What is the ICD-9 equivalent of Q20.4?
Under the General Equivalence Mappings, double inlet ventricle converts to ICD-9-CM 745.3 (common ventricle). The mapping is a direct match.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
