congestive heart failure Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. (Human Disease Ontology, DOID_6000)
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23 genes associated with the disease congestive heart failure in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CLCN6 chloride channel, voltage-sensitive 6 1.12703
USP3 ubiquitin specific peptidase 3 0.52461
LRIG3 leucine-rich repeats and immunoglobulin-like domains 3 0.4215
CMTM7 CKLF-like MARVEL transmembrane domain containing 7 0.345945
TBC1D4 TBC1 domain family, member 4 0.297866
OTUD7A OTU deubiquitinase 7A 0.256228
ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif, 20 0.256228
ADAMTS12 ADAM metallopeptidase with thrombospondin type 1 motif, 12 0.197766
TMTC1 transmembrane and tetratricopeptide repeat containing 1 0.15771
HNRNPA1P4 heterogeneous nuclear ribonucleoprotein A1 pseudogene 4 0.15771
RPUSD4 RNA pseudouridylate synthase domain containing 4 0.15771
GPM6A glycoprotein M6A 0.126165
MOB3B MOB kinase activator 3B 0.100789
GNA15 guanine nucleotide binding protein (G protein), alpha 15 (Gq class) 0.080593
BCHE butyrylcholinesterase 0.080593
PARVA parvin, alpha 0.064973
EVX1 even-skipped homeobox 1 0.064973
HLX H2.0-like homeobox 0.064973
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1 0.064973
PSMC1 proteasome (prosome, macropain) 26S subunit, ATPase, 1 0.064973
C22ORF34 chromosome 22 open reading frame 34 0.064973
CH25H cholesterol 25-hydroxylase 0.052255
IFRD1 interferon-related developmental regulator 1 0.043246