| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | The sternal cleft is a rare congenital anomaly resulting from a fusion failure of the sternum. (Human Phenotype Ontology, HP_0010309) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010309 |
| Similar Terms | |
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1 genes associated with the bifid sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RPS6KA3 | ribosomal protein S6 kinase, 90kDa, polypeptide 3 |
