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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

10 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Digestive system disorder (141) Achalasia (31) Esophageal disorder (20) Human disease (14) Upper digestive tract disorder (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 4 Not yet recruiting 2 Not yet finished but already full! 1 Completed 3
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