congenital diaphragmatic hernia
MeSH: D065630ORPHA: 2140
Overview
diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with congenital diaphragmatic hernia, sourced from HPO and Orphanet clinical annotations.
Congenital diaphragmatic herniaProminent sternumPulmonary hypoplasiaRespiratory distressIntestinal malrotationAplasia/Hypoplasia of the diaphragmHypoxemiaAbnormal cardiovascular system morphology
Classification & Codes
MeSH Code
D065630Orphanet Code
ORPHA:2140congenital diaphragmatic hernia
| MeSH | D065630 |
| Orphanet | ORPHA:2140 |
| Treatments | 0 drug(s) |
| Symptoms on record | 8 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO