|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A notched form of the helix of the ear. That is, a defect in the continuity of the helix, which may occur at any point along its length. (Human Phenotype Ontology, HP_0009902)|
|Downloads & Tools|
2 genes associated with the cleft helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.