Abruptio Placentae Gene Set

Dataset	CTD 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)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D000037
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Genes

5 genes/proteins associated with the disease Abruptio Placentae from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
BHMT	betaine--homocysteine S-methyltransferase	2.88009
NOS3	nitric oxide synthase 3 (endothelial cell)	2.88009
MTHFD1	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase	2.88009
CAPZB	capping protein (actin filament) muscle Z-line, beta	1.10872
GNB1	guanine nucleotide binding protein (G protein), beta polypeptide 1	1.02634