Human genes for achalasia
Achalasia [DOID:9164]
An esophageal disease that is characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing.
Synonyms: achalasia, achalasias, DOID:9164, achalasia of cardia, achalasia of esophagus ...
Linkouts: OMIM