hydroxyprolinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of hydroxyproline in the blood. (Human Phenotype Ontology, HP_0003260)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003260
Similar Terms
Downloads & Tools

Genes

1 genes associated with the hydroxyprolinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b