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Achalasia, familial esophageal

MONDO:0100457

An instance of achalsia that is caused by an inherited genomic modification in an individual.

Also known as: achalasia, familial esophageal

6 clinical trials for this condition and its sub-types, 0 tagged with Achalasia, familial esophageal itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18235) ↑ Achalasia (43)

Including sub-types (6) Tagged with Achalasia, familial esophageal (0)

Trials to join now! 4 Not yet recruiting 1 Completed 1

Hypnosis as a hospital treatment for gut disorders?

Symptom relief Not yet recruiting

This pilot study compares recorded gut-directed hypnosis to an educational recording for hospitalized patients with chronic gut problems, such as irritable bowel syndrome or inflammatory bowel disease. Participants listen to the recordings over the phone while in the hospital for…

Sponsor: Stanford University • Aim: Symptom relief

Last updated Jul 02, 2026 00:00 UTC