2026 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
- 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 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 299 through 301. 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 other POA exempt codes.
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
- 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
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Congenital aneurysm, specified site NEC
- Spinal vessel anomaly
Type 2 Excludes
- disorders of pyrophosphate metabolism E83.82
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.
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Agenesis
- ductus arteriosus - Q28.8
- Pseudoarteriosus - Q28.8
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Absence(of) (organ or part) (complete or partial)
- ductus arteriosus
- Agenesis
- ductus arteriosus
- Anomaly, anomalous(congenital) (unspecified type)
- cardiovascular system
- Pseudoarteriosus
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Tetralogy of Fallot
a combination of congenital heart defects consisting of four key features including ventricular septal defects; pulmonary stenosis; right ventricular hypertrophy; and a dextro-positioned aorta. in this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing cyanosis.
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
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, 2025 through September 30, 2026.
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 299, 300, 301, with relative weights from 0.7197 to 1.6327 depending on complications. Higher weights mean higher Medicare reimbursement.
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.
What is the ICD-9 equivalent of Q28.8?
Under the General Equivalence Mappings, other specified congenital malformations of circulatory system converts to ICD-9-CM 747.89 (circulatory anomaly NEC). The mapping is approximate, so confirm the match fits the documentation.
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.
