|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of a supernumerary, i.e. third, crus of the helix (FMA:61024) in the helix, arising at or above the normal bifurcation of the antihelix. (Human Phenotype Ontology, HP_0100015)|
|Downloads & Tools|
2 genes associated with the stahl ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.