Overview
Congenital emphysema 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.
Laboured breathing
Very frequent (80-99%)HP:0002098
Pulmonary emphysema
Very frequent (80-99%)HP:0002097
Abnormality of immune system physiology
Frequent (30-79%)HP:0010978
Blue discoloration of the skin
Frequent (30-79%)HP:0000961
Mediastinal shift
Frequent (30-79%)HP:6000012
Panting
Frequent (30-79%)HP:0002094
Racing heart
Frequent (30-79%)HP:0001649
Wheezing
Frequent (30-79%)HP:0030828
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Asymmetry of the thorax
Occasional (5-29%)HP:0001555
Feeding difficulties
Occasional (5-29%)HP:0011968
Postnatal failure to thrive
Occasional (5-29%)HP:0001508
Pulmonary atelectasis
Occasional (5-29%)HP:0100750
Bronchial cartilage hypoplasia
HP:0006539
Quick Facts
- SNOMED CT
- 47895001
- UMLS CUI
- C0265797
- Fully Specified Name
- Congenital emphysema (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.