|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A gap (cleft) affecting one of the alveolar ridges. (Human Phenotype Ontology, HP_0010289)|
|Downloads & Tools|
1 genes associated with the alveolar ridge cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|EIF4A3||eukaryotic translation initiation factor 4A3|