Sporadic primary achalasia (Q101592): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/505440999 / rank | |||
Normal rank | |||
Revision as of 18:25, 16 August 2026
This is a common type of oesophageal motility disorder of non-inherited form of primary achalasia, involving the smooth muscle layer of the oesophagus and the lower oesophageal sphincter (LES) in the absence of other explanations like cancer or fibrosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_505440999 |
||
| English | Sporadic primary achalasia |
This is a common type of oesophageal motility disorder of non-inherited form of primary achalasia, involving the smooth muscle layer of the oesophagus and the lower oesophageal sphincter (LES) in the absence of other explanations like cancer or fibrosis. |
