bifid sternum Gene Set

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
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Genes

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