|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital malformation with a cleft (gap or opening) in the midline of the face. (Human Phenotype Ontology, HP_0100629)|
|Downloads & Tools|
5 genes associated with the midline facial cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.