Catalog

Familial primary achalasia

No MMS code

Link to WHO Definition

Familial primary achalasia – http://id.who.int/icd/entity/265869596

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.