palindromic rheumatism Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A syndrome that involves sudden and rapidly developing attacks of arthritis with a remission period that results_in no joint damage or symptoms. (Human Disease Ontology, DOID_1166)
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Genes

14 genes co-occuring with the disease palindromic rheumatism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
MEFV	Mediterranean fever	1.22779
DYNLT1	dynein, light chain, Tctex-type 1	0.743141
PRTN3	proteinase 3	0.699517
PADI4	peptidyl arginine deiminase, type IV	0.654463
HLA-A	major histocompatibility complex, class I, A	0.583941
HLA-B	major histocompatibility complex, class I, B	0.400453
PTPN22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	0.378885
ERBB3	erb-b2 receptor tyrosine kinase 3	0.335778
CRP	C-reactive protein, pentraxin-related	0.332121
PTPN12	protein tyrosine phosphatase, non-receptor type 12	0.30342
PTPRD	protein tyrosine phosphatase, receptor type, D	0.296931
MRAP	melanocortin 2 receptor accessory protein	0.247501
TNFRSF1A	tumor necrosis factor receptor superfamily, member 1A	0.231448
PTPN11	protein tyrosine phosphatase, non-receptor type 11	0.179802