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Congenital lobar emphysema

disorder
SNOMED 66987001CUI C0265797

Overview

Congenital lobar 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
Poor weight gain
Occasional (5-29%)HP:0001508
Pulmonary atelectasis
Occasional (5-29%)HP:0100750
Bronchial cartilage hypoplasia
HP:0006539

Quick Facts

SNOMED CT
66987001
UMLS CUI
C0265797
Fully Specified Name
Congenital lobar 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.