Catalog
Structural developmental anomalies of oesophagus
Link to WHO Definition
Structural developmental anomalies of oesophagus – http://id.who.int/icd/entity/1999264345
Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly in type and severity, and are caused by a wide variety of determining factors, including genetic mutations, chromosomal aberrations, teratogenic agents, and environmental factors. Most developmental defects are apparent at birth, especially any structural malformation, but some become evident later.
Parents
Children
- LB12.2 Oesophageal fistula without atresia
- Congenital oesophageal hyperplasia
- Duplication of oesophagus
- Congenital displacement of oesophagus
- LB12.1 Atresia of oesophagus
- LB12.3 Congenital stenosis or stricture of oesophagus
- Congenital short oesophagus
- Bronchopulmonary foregut malformation
- LB12.5 Congenital dilatation of oesophagus
- Congenital chalasia
- LB12.0 Congenital oesophageal web or ring
- Congenital achalasia
- LB12.4 Congenital diverticulum of oesophagus
- Heterotopic gastric mucosa
- Absence of oesophagus