|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||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. (Human Disease Ontology, DOID_9164)|
|Downloads & Tools|
2 genes/proteins associated with the disease Esophageal Achalasia from the curated CTD Gene-Disease Associations dataset.