absent sternal ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of formation of mineralized bony tissue of the sternum. (Human Phenotype Ontology, HP_0006628)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006628
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Genes

4 genes associated with the absent sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FIG4 FIG4 phosphoinositide 5-phosphatase
ORC1 origin recognition complex, subunit 1
ORC6 origin recognition complex, subunit 6
SOX9 SRY (sex determining region Y)-box 9