Congenital oesophageal web or ring (Q46316): Difference between revisions
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13 August 2026
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| Property / Linked ICD 10: Q39.4 / rank | |||||||||||||||
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Latest revision as of 14:49, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB12.0 |
||
| English | Congenital oesophageal web or ring |
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. |
Statements
CID11:LB12.0
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dki-india-LB12.0
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Concluído
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13 August 2026
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