paraphilia disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
EGOT eosinophil granule ontogeny transcript (non-protein coding) 1.85182
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 1.26473
METTL13 methyltransferase like 13 1.11141
KHDRBS3 KH domain containing, RNA binding, signal transduction associated 3 1.09041
ADD2 adducin 2 (beta) 1.07992
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group) 1.05303
PNP purine nucleoside phosphorylase 0.987693
MAOA monoamine oxidase A 0.94078
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4 0.920085
MARS methionyl-tRNA synthetase 0.799513
GRN granulin 0.56722
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 0.519961
MAOB monoamine oxidase B 0.443171
CBS cystathionine-beta-synthase 0.435275
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) 0.365193
IFNB1 interferon, beta 1, fibroblast 0.286877