|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of an abnormally prominent of the crus of the helix (FMA:61024). That is, development of the crus helix to the same degree as an average antihelix stem or helix. (Human Phenotype Ontology, HP_0009899)|
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2 genes associated with the prominent crus of helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.