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