2027 ICD-10-CM Diagnosis Code Q25.29Other atresia of aorta
ICD-10-CM Codes›Q00-Q99›Q20-Q28›Q25
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- POA Exempt
- Chronic Condition
Q25.29 is a billable ICD-10-CM diagnosis code for other atresia of aorta. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 306 through 307. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 55 closely related codes. 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
Q25.29 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Congenital malformations of the circulatory system (Q20-Q28).
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Aortic arch hypoplasia between subclavian and common carotid arteries
- Ascending aortic atresia
- Atresia and stenosis of aorta
- Atresia of aortic arch with fibrous cord
- Atresia of aortic arch with fibrous cord between left common carotid artery and right common carotid artery
- Atresia of aortic arch with fibrous cord between subclavian artery and common carotid artery
- Atresia of aortic arch with fibrous cord distal to subclavian artery
- Congenital atresia of aorta
- Congenital atresia of aortic arch
- Congenital hypoplasia of aortic arch
- Congenital luminal atresia of aortic arch between left common carotid artery and right common carotid artery
- Congenital luminal atresia of aortic arch between subclavian artery and common carotid artery
- Congenital luminal atresia of aortic arch distal to subclavian artery
- Congenital stenosis of aorta
- Developmental malformation of branchial arch
- Double aortic arch with left arch dominant
- Double aortic arch with left arch dominant and atresia of right arch
- Double aortic arch with right arch dominant
- Double aortic arch with right arch dominant and atresia of left arch
- Double aortic arch with right arch dominant and atresia of left arch and left ligament to diverticulum
- Muscular subvalvar atresia of aorta
- Persisting fifth aortic arch
- Persisting fifth aortic arch with atresia of fourth arch
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to Q25.29: its own notes plus those printed at Chapter 17. A note printed at a category, block or chapter applies to every code under it.
Applicable To
Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.
- Atresia of aorta
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
Notes
General instructions on how these codes are used.
- Codes from this chapter are not for use on maternal records
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
aorta (ring) Q25.29
Malformation (congenital) See Also: Anomaly;
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 Q25.29 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code History & ChangesHistory
Replacement Q25.29 replaces the following previously assigned code(s):
- Q25.2 - Atresia of aorta
Questions About Q25.29Overview
What is the ICD-10 code for other atresia of aorta?
The ICD-10-CM code for other atresia of aorta is Q25.29 (sometimes written as Q2529). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is Q25.29 (Atresia of aorta) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other atresia of aorta on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does Q25.29 group to?
When other atresia of aorta is the principal diagnosis on an inpatient stay, it groups to MS-DRG 306, 307, with relative weights from 0.9146 to 1.5457 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q25.29 a CC or MCC?
CMS lists Q25.29 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 55 closely related codes in its exclusion list.
Is Q25.29 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 other atresia of aorta on inpatient claims. The code appears in the Congenital malformations of the circulatory system (Q20-Q28) range of the CMS exempt list.