endocardial fibroelastosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An endocardium disease that is characterized by a thickening of the inmost lining of the heart chambers due to an increase in the amount of supporting connective tissue and elastic fibers. (Human Disease Ontology, DOID_12929)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001706
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Genes

6 genes associated with the endocardial fibroelastosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTN2 actinin, alpha 2
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
GJA5 gap junction protein, alpha 5, 40kDa
IDUA iduronidase, alpha-L-
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
TAZ tafazzin