intermittent explosive disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An impulse control disorder that involves the episodic inability to control violent impulses with a disproportionate degree of aggressiveness. (Human Disease Ontology, DOID_12401)
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Genes

9 genes co-occuring with the disease intermittent explosive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CGA glycoprotein hormones, alpha polypeptide 1.89036
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled 1.25297
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) 1.13459
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.01385
CHRFAM7A CHRNA7 (cholinergic receptor, nicotinic, alpha 7, exons 5-10) and FAM7A (family with sequence similarity 7A, exons A-E) fusion 0.909376
ADRB1 adrenoceptor beta 1 0.828229
TPH1 tryptophan hydroxylase 1 0.750457
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 0.673518
NPY neuropeptide Y 0.474498