dilated cardiomyopathy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An intrinsic cardiomyopathy that results in damage to the myocardium causing the heart to pump blood inefficiently and characterized by an enlarged heart. (Human Disease Ontology, DOID_12930)
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8 genes associated with the disease dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DMD dystrophin
LMNA lamin A/C
MYH7 myosin, heavy chain 7, cardiac muscle, beta
PDLIM3 PDZ and LIM domain 3
SCN5A sodium channel, voltage gated, type V alpha subunit
TCAP titin-cap
TNNT2 troponin T type 2 (cardiac)