premature rupture of membranes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Premature rupture of membranes (PROM) is a condition which occurs in pregnancy when the amniotic sac ruptures more than an hour before the onset of labor. (Human Phenotype Ontology, HP_0001788)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001788
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Genes

8 genes associated with the premature rupture of membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
COL1A1 collagen, type I, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
LMNA lamin A/C
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
ZMPSTE24 zinc metallopeptidase STE24