Disease: Schnitzler Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schnitzler Syndrome
CUI: C0524988
Disease: Schnitzler Syndrome
0.010 GeneticVariation BEFREE Time-course analysis of serum hepcidin, iron and cytokines in a C282Y homozygous patient with Schnitzler's syndrome treated with IL-1 receptor antagonist. 19608676 2009