primary syphilis Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A syphilis that is the first stage of syphilis, marked by the development of a chancre, which is characterized by mononuclear leukocytic infiltration, macrophages, and lymphocytes. (Human Disease Ontology, DOID_4156)
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Genes

13 genes co-occuring with the disease primary syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
EXTL3	exostosin-like glycosyltransferase 3	2.032
PDE6D	phosphodiesterase 6D, cGMP-specific, rod, delta	1.30357
ZBTB32	zinc finger and BTB domain containing 32	1.23733
TPR	translocated promoter region, nuclear basket protein	1.17808
MAPK1	mitogen-activated protein kinase 1	0.739082
CD4	CD4 molecule	0.617486
PRRC2A	proline-rich coiled-coil 2A	0.467306
CD22	CD22 molecule	0.459373
SRY	sex determining region Y	0.43227
LYZ	lysozyme	0.205916
CD79A	CD79a molecule, immunoglobulin-associated alpha	0.18472
B2M	beta-2-microglobulin	0.171535
IL10	interleukin 10	0.171286