Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Laryngeal stenosis
Very frequent (80-99%)HP:0001602
Atria septal defect
Frequent (30-79%)HP:0001631
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Related Conditions
Combined valvular-subvalvular pulmonic stenosis(child)
Fallot's trilogy(child)
Tetralogy of Fallot(child)
Prune belly syndrome with pulmonic stenosis, mental retardation and deafness(child)
Pulmonic stenosis and congenital nephrosis(child)
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect and pulmonary stenosis Fallot type(child)
Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis Fallot type(child)
Congenital pulmonary valve abnormality(parent)
Pulmonic valve stenosis(parent)
Congenital stenosis of cardiac valve(parent)
Quick Facts
- SNOMED CT
- 67278007
- UMLS CUI
- C0162164
- Fully Specified Name
- Congenital stenosis of pulmonary valve (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 3
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.