Disease: Lofgrens syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Lofgrens syndrome
CUI: C0340164
Disease: Lofgrens syndrome
0.010 GeneticVariation BEFREE We found independent genetic risk factors in clinically distinct disease phenotypes: BTNL2 rs2076530 A allele in patients without Löfgren syndrome or with isolated thoracic disease, and HLA-DRB1*03 in Löfgren syndrome or disease resolution. 23017494 2012