pericardial effusion Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity. (Human Disease Ontology, DOID_118)
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6 genes associated with the pericardial effusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
CCBE1 collagen and calcium binding EGF domains 1
LMNA lamin A/C
PMM2 phosphomannomutase 2
PTPN14 protein tyrosine phosphatase, non-receptor type 14
SMAD4 SMAD family member 4