|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the crus of the helix (FMA:61024), which is the horizontal piece of cartilage located outside the ear canal that divides the upper and lower parts of the ear. (Human Phenotype Ontology, HP_0009895)|
|Downloads & Tools|
2 genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.