proximal femoral metaphyseal abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the metaphysis of the proximal femur (close to the hip). (Human Phenotype Ontology, HP_0006431)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006431
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Genes

2 genes associated with the proximal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL10A1 collagen, type X, alpha 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4