Esophageal Stenosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormal narrowing of the lumen of the esophagus. (Human Phenotype Ontology, HP_0010450)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D004940
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Genes

1 genes/proteins associated with the disease Esophageal Stenosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SOD2 superoxide dismutase 2, mitochondrial 2.88009