Overview
Congenital atrial septal defect is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Atria septal defect
Very frequent (80-99%)HP:0001631
Patent ostium secundum
Very frequent (80-99%)HP:0001684
Quivering upper heart chambers resulting in irregular heartbeat
Frequent (30-79%)HP:0005110
Systolic heart murmur
Frequent (30-79%)HP:0031664
Atrial flutter
Occasional (5-29%)HP:0004749
Atrial septal defect, primum type
Occasional (5-29%)HP:0010445
Cardiac insufficiency
Occasional (5-29%)HP:0001635
Complete right bundle branch block
Occasional (5-29%)HP:0011712
Electrical right axis deviation
Occasional (5-29%)HP:0033567
Exertional dyspnea
Occasional (5-29%)HP:0002875
Increased heart size
Occasional (5-29%)HP:0001640
Palpitations
Occasional (5-29%)HP:0001962
Pulmonary artery hypertension
Occasional (5-29%)HP:0002092
respiratory infections, recurrent
Occasional (5-29%)HP:0002205
Right ventricular dilatation
Occasional (5-29%)HP:0005133
Sinus venosus atrial septal defect
Occasional (5-29%)HP:0011567
Tiredness
Occasional (5-29%)HP:0012378
Cerebral vascular events
Very rare (1-4%)HP:0001297
Coronary sinus atrial septal defect
Very rare (1-4%)HP:0011643
Aortic stenosis
HP:0001650
Atrial septal dilatation
HP:0011995
Bicuspid aortic valve
HP:0001647
Narrowing of blood vessel below aortic heart valve
HP:0001682
PLSVC
HP:0005301
Second degree atrioventricular block
HP:0011706
Tetralogy of Fallot with pulmonary atresia
HP:0012516
VSD
HP:0001629
Related Conditions
Atrial septal defect with endocardial cushion defect, partial type(child)
Patent ostium secundum(child)
Lutembacher's syndrome(child)
Restrictive interatrial communication with obligatory shunt(child)
Interatrial communication through coronary sinus orifice(child)
Atrial septal defect, atrioventricular conduction defect syndrome(child)
Lymphedema, atrial septal defect, facial changes syndrome(child)
Ebstein's anomaly with atrial septal defect(child)
Fallot's trilogy(child)
Ostium primum defect(child)
Pentalogy of Fallot(child)
Atrial septal defect through coronary sinus orifice(child)
Ostium secundum type atrial septal defect(child)
Atrial septal defect(parent)
Congenital septal defect of heart(parent)
Congenital abnormality of atrial septum(parent)
Quick Facts
- SNOMED CT
- 405752007
- UMLS CUI
- C0018817
- Fully Specified Name
- Congenital atrial septal defect (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 27
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.