Esophageal atresia
Esophageal atresia
Definition
A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and symptoms in a newborn with this abnormality include excessive salivation, choking, coughing, and the development of cyanosis and respiratory distress when fed.
Also known as congenital atresia of esophagus, congenital atresia of oesophagus, congenital esophageal atresia, congenital imperforate oesophagus, esophageal atresia, esophageal atresia (disease), imperforate oesophagus — per MONDO
Also identified as
- DOID 10485 per MONDO
- ICD9 750.3 per MONDO
- MESH D004933 per MONDO
- NCIT C87072 per MONDO
- SCTID 26179002 per MONDO
- UMLS C0014850 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Alimentary part of gastrointestinal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Alimentary part of gastrointestinal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Esophagus | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Esophagus | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |