delusional disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A psychotic disorder that involves an uncommon psychiatric condition in which patients present with circumscribed symptoms of non-bizarre delusions, but with the absence of prominent hallucinations and no thought disorder, mood disorder, or significant flattening effect. (Human Disease Ontology, DOID_778)
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22 genes co-occuring with the disease delusional disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
DRD4 dopamine receptor D4 1.62291
FMO3 flavin containing monooxygenase 3 1.23429
DRD2 dopamine receptor D2 1.1755
CYP2D7 cytochrome P450, family 2, subfamily D, polypeptide 7 (gene/pseudogene) 1.0463
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.03535
DRD3 dopamine receptor D3 0.985164
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 0.804436
PDSS1 prenyl (decaprenyl) diphosphate synthase, subunit 1 0.738676
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 0.717635
TES testin LIM domain protein 0.541605
PYY peptide YY 0.483985
HLA-E major histocompatibility complex, class I, E 0.471846
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.453339
PNP purine nucleoside phosphorylase 0.442418
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic 0.397843
GLS2 glutaminase 2 (liver, mitochondrial) 0.36741
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 0.356341
MAPK14 mitogen-activated protein kinase 14 0.332852
PRRC2A proline-rich coiled-coil 2A 0.317909
BCHE butyrylcholinesterase 0.241895
PPIG peptidylprolyl isomerase G (cyclophilin G) 0.229024
NPY neuropeptide Y 0.19582