abnormality of the femoral metaphysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the femoral metaphysis. (Human Phenotype Ontology, HP_0006489)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006489
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5 genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL10A1 collagen, type X, alpha 1
FGFR3 fibroblast growth factor receptor 3
SETBP1 SET binding protein 1
TRIP11 thyroid hormone receptor interactor 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4