esophageal stenosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal narrowing of the lumen of the esophagus. (Human Phenotype Ontology, HP_0010450)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010450
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Genes

3 genes associated with the esophageal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL7A1 collagen, type VII, alpha 1
DKC1 dyskeratosis congenita 1, dyskerin
NOP10 NOP10 ribonucleoprotein