Polyhydramnios Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A placenta disease that is characterized by an excess of amniotic fluid in the amniotic sac. (Human Disease Ontology, DOID_8488)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006831
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Genes

1 genes/proteins associated with the disease Polyhydramnios from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IGF2 insulin-like growth factor 2 2.88009