LB12.0 Congenital oesophageal web or ring
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A rare form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut that presents as a mucosal lesion forming an incomplete diaphragm. Symptoms (apparent from birth) include dysphagia, regurgitation, and choking.
exclusions
synonyms
- Congenital oesophageal web or ring
- Congenital web of oesophagus
- congenital webbed oesophagus
- Congenital ring of oesophagus
- Congenital Schatzki ring
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