abruptio placentae Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A placenta disease that is characterized by separation of the placental lining from the uterus of the mother. (Human Disease Ontology, DOID_9667)
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3 genes associated with the disease abruptio placentae in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
IL1RN interleukin 1 receptor antagonist
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)