thickened cortex of bones Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An Abnormality of cortical bone leading to an abnormal thickness of the cortex of affected bones. (Human Phenotype Ontology, HP_0100039)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100039
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Genes

6 genes associated with the thickened cortex of bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FAM111A family with sequence similarity 111, member A
LIFR leukemia inhibitory factor receptor alpha
LRP5 low density lipoprotein receptor-related protein 5
SETBP1 SET binding protein 1
SOST sclerostin
TGFB1 transforming growth factor, beta 1