|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Incomplete fusion of the chin, resulting from a developmental defect and manifesting as a midline cleft or fissure of the chin. (Human Phenotype Ontology, HP_0011323)|
|Downloads & Tools|
2 genes associated with the cleft of chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.