Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Diaphragmatic hernia
Very frequent (80-99%)HP:0000776
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Absent/underdeveloped diaprhagm
Frequent (30-79%)HP:0010315
Hypoxia
Frequent (30-79%)HP:0012418
Intestinal malrotation
Frequent (30-79%)HP:0002566
Laboured breathing
Frequent (30-79%)HP:0002098
Poorly developed lungs
Frequent (30-79%)HP:0002089
Sternal protrusion
Frequent (30-79%)HP:0000884
Related Conditions
Congenital hernia of foramen of Morgagni(child)
Congenital posterolateral diaphragmatic hernia(child)
Pericardial and diaphragmatic defect syndrome(child)
Fryns syndrome(child)
Lethal hydranencephaly, diaphragmatic hernia syndrome(child)
Congenital brachyoesophagus, intrathoracic stomach, vertebral anomalies syndrome(child)
Diaphragmatic hernia, short bowel, asplenia syndrome(child)
Congenital hiatus hernia(child)
Congenital anomaly of diaphragm(parent)
Diaphragmatic hernia(parent)
Quick Facts
- SNOMED CT
- 17190001
- UMLS CUI
- C0235833
- Fully Specified Name
- Congenital diaphragmatic hernia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.