Endocardial Fibroelastosis Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
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	https://www.disgenet.org/browser/0/1/0/C0014117
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Genes

11 genes associated with the disease Endocardial Fibroelastosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ACTN2	actinin, alpha 2
BMP7	bone morphogenetic protein 7
CSRP3	cysteine and glycine-rich protein 3 (cardiac LIM protein)
ELN	elastin
GJA5	gap junction protein, alpha 5, 40kDa
IDUA	iduronidase, alpha-L-
MYH7	myosin, heavy chain 7, cardiac muscle, beta
NEBL	nebulette
SLC22A5	solute carrier family 22 (organic cation/carnitine transporter), member 5
SSB	Sjogren syndrome antigen B (autoantigen La)
TAZ	tafazzin