esophageal achalasia; Gene Set

Dataset GAD 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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Genes

1 genes associated with the disease esophageal achalasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
NOS2 nitric oxide synthase 2, inducible