uterine prolapse Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of prolapse of the uterus. (Human Phenotype Ontology, HP_0000139)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000139
Similar Terms
Downloads & Tools


3 genes associated with the uterine prolapse phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL3A1 collagen, type III, alpha 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SMAD3 SMAD family member 3