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ICD-10-CM Codes
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Q00-Q99
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Q20-Q28
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Q20-
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2023 ICD-10-CM Diagnosis Code Q20.1
2023 ICD-10-CM Diagnosis Code Q20.1
Double outlet right ventricle
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
- Q20.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q20.1 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q20.1 - other international versions of ICD-10 Q20.1 may differ.
The following code(s) above
Q20.1 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q20.1:
- A rare congenital cardiovascular abnormality in which both the aorta and the pulmonary artery arise from the right ventricle.
- A subtype with pulmonary ventricular septal defect.
- Incomplete transposition of the great vessels in which both the aorta and the pulmonary artery arise from the right ventricle. The only outlet of the left ventricle is a large ventricular septal defect (ventricular septal defects or vsd). The various subtypes are classified by the location of the septal defect, such as subaortic, subpulmonary, or noncommitted.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q20.1 is considered exempt from POA reporting.
ICD-10-CM Q20.1 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 306 Cardiac congenital and valvular disorders with mcc
- 307 Cardiac congenital and valvular disorders without mcc
Convert Q20.1 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- Complex
- Taussig-Bing Q20.1 (transposition, aorta and overriding pulmonary artery)
- Defect, defective Q89.9
ICD-10-CM Diagnosis Code Q89.9
Congenital malformation, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
Applicable To- Congenital anomaly NOS
- Congenital deformity NOS
- Taussig-Bing Q20.1 (aortic transposition and overriding pulmonary artery)
- Double
- Origin of both great vessels from right ventricle Q20.1
- Taussig-Bing syndrome Q20.1
ICD-10-CM Codes Adjacent To Q20.1
Q18.2 Other branchial cleft malformations
Q18.8 Other specified congenital malformations of face and neck
Q18.9 Congenital malformation of face and neck, unspecified
Q20 Congenital malformations of cardiac chambers and connections
Q20.0 Common arterial trunk
Q20.1
Double outlet right ventricle
Q20.2 Double outlet left ventricle
Q20.3 Discordant ventriculoarterial connection
Q20.4 Double inlet ventricle
Q20.5 Discordant atrioventricular connection
Q20.6 Isomerism of atrial appendages
Q20.8 Other congenital malformations of cardiac chambers and connections
Q20.9 Congenital malformation of cardiac chambers and connections, unspecified
Q21 Congenital malformations of cardiac septa
Q21.0 Ventricular septal defect
Q21.1 Atrial septal defect
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
