| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009899 |
| Similar Terms | |
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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.
