SELPLG, selectin P ligand, 6404

N. diseases: 113; N. variants: 1
Disease: Behcet Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 GeneticVariation disease BEFREE PSGL-1 VNTR polymorphism may have limited contribution to the thrombotic tendency in patients with BD. 28809090 2018