Familial primary achalasia (Q101591): Difference between revisions
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Revision as of 18:25, 16 August 2026
Familial oesophageal achalasia is an inherited form of primary achalasia, a disorder of oesophageal mobility, and is characterised by dysphagia due to the inability of the lower oesophageal sphincter to relax.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_265869596 |
||
| English | Familial primary achalasia |
Familial oesophageal achalasia is an inherited form of primary achalasia, a disorder of oesophageal mobility, and is characterised by dysphagia due to the inability of the lower oesophageal sphincter to relax. |
Statements
CID11:ID_265869596
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