endocardial fibroelastosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
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)
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Genes

20 genes co-occuring with the disease endocardial fibroelastosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TAZ tafazzin 1.76094
NEBL nebulette 1.40876
CA5B carbonic anhydrase VB, mitochondrial 1.25776
ACTN2 actinin, alpha 2 1.24558
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein) 1.07026
BLVRA biliverdin reductase A 1.0648
GAA glucosidase, alpha; acid 0.919673
GAB2 GRB2-associated binding protein 2 0.84585
TROVE2 TROVE domain family, member 2 0.798282
A1BG alpha-1-B glycoprotein 0.732191
IDUA iduronidase, alpha-L- 0.696306
TRIM21 tripartite motif containing 21 0.590558
FABP3 fatty acid binding protein 3, muscle and heart 0.586276
GRB2 growth factor receptor-bound protein 2 0.511112
ANGPT1 angiopoietin 1 0.499614
MIB1 mindbomb E3 ubiquitin protein ligase 1 0.490835
MBTPS1 membrane-bound transcription factor peptidase, site 1 0.471468
ZYX zyxin 0.444676
GZMB granzyme B (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1) 0.369258
TNNT2 troponin T type 2 (cardiac) 0.210925