|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A benign uni- or multicystic, intraosseous tumor of odontogenic origin, with a characteristic lining of parakeratinized stratified squamous epithelium and potential for aggressive, infiltrative behaviour. (Human Phenotype Ontology, HP_0010603)|
|Downloads & Tools|
3 genes associated with the keratocystic odontogenic tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.