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Dictionary » Familial esophageal achalasia
 

Familial esophageal achalasia

Introduction: Familial esophageal achalasia

Description of Familial esophageal achalasia

Familial esophageal achalasia (medical condition): A rare familial disorder where the esophagus lacks the normal...more »

See also:

Achalasia, familial esophageal:
  »Introduction: Achalasia, familial esophageal
  »Symptoms of Achalasia, familial esophageal

Familial esophageal achalasia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial esophageal achalasia:

Familial esophageal achalasia: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Familial esophageal achalasia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Familial esophageal achalasia, or a subtype of Familial esophageal achalasia, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Familial esophageal achalasia as a Disease

Familial esophageal achalasia: Another name for Achalasia, familial esophageal (or close medical condition association).
  »Introduction: Achalasia, familial esophageal
  »Symptoms of Achalasia, familial esophageal

Familial esophageal achalasia: Related Diseases

Familial esophageal achalasia: Familial esophageal achalasia is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial esophageal achalasia (Achalasia, familial esophageal)

Some of the symptoms of Familial esophageal achalasia incude:

Terms associated with Familial esophageal achalasia:

Terms Similar to Familial esophageal achalasia:

Source - NIH

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