| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A pathological narrowing of the esophagus that is caused by the development of a ring of scar tissue that constricts the esophageal lumen. (Human Phenotype Ontology, HP_0002043) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0002043 |
| Similar Terms | |
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3 genes associated with the esophageal stricture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
