cardiac edema Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal accumulation of fluid in the interstitial tissues and cavities of the body due to impaired cardiac function or congestive heart failure; usually characterized by increased venous and capillary pressures and often associated with renal sodium retention (Mammalian Phenotype Ontology, MP_0012270)
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7 gene mutations causing the cardiac edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
CLU clusterin
CLUAP1 clusterin associated protein 1
PNPLA2 patatin-like phospholipase domain containing 2
PTPRB protein tyrosine phosphatase, receptor type, B
RDH10 retinol dehydrogenase 10 (all-trans)
TRAF3IP1 TNF receptor-associated factor 3 interacting protein 1