2027 ICD-10-CM Diagnosis Code Q28.8Other specified congenital malformations of circulatory system
ICD-10-CM Codes›Q00-Q99›Q20-Q28›Q28
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- POA Exempt
- Chronic Condition
Q28.8 is a billable ICD-10-CM diagnosis code for other specified congenital malformations of circulatory system. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 299 through 301. 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 30 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
Q28.8 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.
- Abnormality of arterial ligament
- Absent venous duct
- Absent venous duct with direct connection of umbilical vein to inferior caval vein
- Absent venous duct with direct connection of umbilical vein to renal vein
- Absent venous duct with direct connection of umbilical vein to right atrium
- Agenesis of artery
- Anomalous insertion of arterial ligament
- Anomalous insertion of arterial ligament into distal left pulmonary artery
- Anomalous insertion of arterial ligament into pulmonary trunk
- Anomalous insertion of arterial ligament into right pulmonary artery
- Anomalous origin of arterial ligament
- Anomalous origin of arterial ligament from aortic arch
- Anomalous origin of arterial ligament from aortic diverticulum
- Anomalous origin of arterial ligament from ascending aorta
- Anomalous origin of arterial ligament from distal descending aorta
- Anomalous origin of arterial ligament from left brachiocephalic artery
- Anomalous origin of arterial ligament from left carotid artery
- Anomalous origin of arterial ligament from left subclavian artery
- Anomalous origin of arterial ligament from retroesophageal aortic diverticulum
- Anomalous origin of arterial ligament from right aortic arch
- Anomalous origin of arterial ligament from right brachiocephalic artery
- Anomalous origin of arterial ligament from right carotid artery
- Anomalous origin of arterial ligament from right subclavian artery
- Anomalous origin of arterial ligament from unknown site
- Anomalous origin of right arterial ligament from left aortic arch
- Anomalous origin of right arterial ligament from right aortic arch
- 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
- Cardiovascular abnormality due to anomalous origin of arterial duct
- Cardiovascular abnormality due to anomalous origin of coronary artery from pulmonary artery
- Cardiovascular abnormality due to anomalous origin of coronary artery orifice
- Cardiovascular abnormality due to bilateral arterial ducts
- Closed ductus venosus
- Congenital absence of ductus arteriosus
- Congenital absence of pulmonary valve
- Congenital anomaly of cardiovascular structure of trunk
- Congenital anomaly of great vessel
- Congenital anomaly of lymphatic structure of trunk
- Congenital atresia of aortic arch
- Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
- Ductus venosus abnormality
- Dural arteriovenous fistula
- Heart disease in mother complicating pregnancy, childbirth AND/OR puerperium
- Hypoplasia of spinal vessel
- Patent ductus venosus
- Pulmonary valve agenesis, tetralogy of Fallot, absence of ductus arteriosus syndrome
- Right arterial ligament
- Structural abnormality of spinal dura mater
- Tetralogy of Fallot
- Type I arteriovenous malformation of spinal cord
- Type II arteriovenous malformation of spinal cord
- Type III arteriovenous malformation of spinal cord
- Type IV arteriovenous malformation of spinal cord
- Venous anomaly of umbilical cord
- Venous remnant
- Venous-lymphatic malformation
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to Q28.8: its own notes plus those printed at Q28 and 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.
- Congenital aneurysm, specified site NEC
- Spinal vessel anomaly
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
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.
- disorders of pyrophosphate metabolism (E83.82-)
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.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name Q28.8, its category, or a range that includes it.
Index to Diseases and InjuriesGuidance
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Birth Defects
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
The full article covers:
- What are birth defects?
- What causes birth defects?
- Who is at risk of having a baby with birth defects?
- How are birth defects diagnosed?
- What are the treatments for birth defects?
- Can birth defects be prevented?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q28.8 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q28.8Overview
What is the ICD-10 code for other specified congenital malformations of circulatory system?
The ICD-10-CM code for other specified congenital malformations of circulatory system is Q28.8 (sometimes written as Q288). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is Q28.8 (Other congenital malformations of circulatory system) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other specified congenital malformations of circulatory system on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does Q28.8 group to?
When other specified congenital malformations of circulatory system is the principal diagnosis on an inpatient stay, it groups to MS-DRG 301, 300, 299, with relative weights from 0.7132 to 1.5840 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q28.8 a CC or MCC?
CMS lists Q28.8 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 30 closely related codes in its exclusion list.
Is Q28.8 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 specified congenital malformations of circulatory system on inpatient claims. The code appears in the Congenital malformations of the circulatory system (Q20-Q28) range of the CMS exempt list.