|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||This term is used for Auriculocondylar syndrome (MIM:602483). Not clear if there is a clean delineation against cleft helix. (Human Phenotype Ontology, HP_0008537)|
|Downloads & Tools|
2 genes associated with the cleft at the superior portion of the pinna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.