Primary dilated cardiomyopathy Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/212110
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Genes

6 genes associated with the Primary dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
BAG3 BCL2-associated athanogene 3
DSP desmoplakin
LMNA lamin A/C
MYH7 myosin, heavy chain 7, cardiac muscle, beta
RBM20 RNA binding motif protein 20
TTN titin