Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Absent pulse
Very frequent (80-99%)HP:0032554
Cardiac murmur
Very frequent (80-99%)HP:0030148
Left ventricular outflow tract obstruction
Very frequent (80-99%)HP:0032092
Blood pressure substantially higher in upper than lower extremities
Frequent (30-79%)HP:0020142
Blue discoloration of the skin
Frequent (30-79%)HP:0000961
Cardiac anomaly
Frequent (30-79%)HP:0001627
Chronic heart failure
Frequent (30-79%)HP:0001635
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
High blood pressure
Frequent (30-79%)HP:0000822
Laboured breathing
Frequent (30-79%)HP:0002098
Left ventricular wall hypertrophy
Frequent (30-79%)HP:0001712
Leg edema
Frequent (30-79%)HP:0010741
Postexertional malaise
Frequent (30-79%)HP:0030973
Shock
Frequent (30-79%)HP:0031273
Systolic heart murmur
Frequent (30-79%)HP:0031664
Tachypnea
Frequent (30-79%)HP:0002789
VSD
Frequent (30-79%)HP:0001629
Abnormal ascending aorta morphology
Occasional (5-29%)HP:0031784
Aortic valve regurgitation
Occasional (5-29%)HP:0001659
Aortopulmonary window
Occasional (5-29%)HP:0011604
Bicuspid aortic valve
Occasional (5-29%)HP:0001647
Exertional dyspnea
Occasional (5-29%)HP:0002875
Headache
Occasional (5-29%)HP:0002315
Increased distance between eyes
Occasional (5-29%)HP:0000316
Intermittent claudication
Occasional (5-29%)HP:0004417
PDA
Occasional (5-29%)HP:0001643
Right bundle-branch block
Occasional (5-29%)HP:0011712
Tricuspid regurgitation
Occasional (5-29%)HP:0005180
Truncus arteriosus
Occasional (5-29%)HP:0001660
Aortic valve atresia
Very rare (1-4%)HP:0010883
Related Conditions
Interrupted aortic arch between left common carotid and brachiocephalic artery(child)
Type A interruption of aortic arch distal to subclavian artery(child)
Type B interruption of aortic arch between subclavian artery and common carotid artery(child)
Interruption of aortic arch between left common carotid artery and right common carotid artery(child)
Common arterial trunk with pulmonary dominance and interrupted aortic arch(child)
Congenital anomaly of aortic arch(parent)
Quick Facts
- SNOMED CT
- 218728005
- UMLS CUI
- C0152419
- Fully Specified Name
- Interrupted aortic arch (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.