right ventricular cardiomyopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Right ventricular dysfunction (global or regional) with functional and morphological right ventricular abnormalities, with or without left ventricular disease. (Human Phenotype Ontology, HP_0011663)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011663
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Genes

9 genes associated with the right ventricular cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DES desmin
DSC2 desmocollin 2
DSG2 desmoglein 2
DSP desmoplakin
JUP junction plakoglobin
PKP2 plakophilin 2
RYR2 ryanodine receptor 2 (cardiac)
TGFB3 transforming growth factor, beta 3
TMEM43 transmembrane protein 43