Sporadic primary achalasia (Q101592)
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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. |
Statements
CID11:ID_505440999
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