Esophageal Achalasia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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2 genes/proteins associated with the disease Esophageal Achalasia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1 2.88009
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1 2.88009