Uterine Hemorrhage Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description presence of bleeding in the uterus; often in response to failed pregnancy (Mammalian Phenotype Ontology, MP_0004898)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014592
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Genes

3 genes/proteins associated with the disease Uterine Hemorrhage from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LHB luteinizing hormone beta polypeptide 1.11255
PRLR prolactin receptor 1.0561
OXT oxytocin/neurophysin I prepropeptide 1.05535