laryngeal cleft Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Presence of a gap in the posterior laryngotracheal wall with a continuity between the larynx and the esopahagus. (Human Phenotype Ontology, HP_0008751)
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2 genes associated with the laryngeal cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EDN1 endothelin 1
GLI3 GLI family zinc finger 3