familial mediterranean fever Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A hypersensitivity reaction type II disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; caused by mutations in the MEFV gene, which encodes the protein pyrin. (Human Disease Ontology, DOID_2987)
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Genes

11 genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1
C5AR1	complement component 5a receptor 1
F2	coagulation factor II (thrombin)
F5	coagulation factor V (proaccelerin, labile factor)
HLA-DQB1	major histocompatibility complex, class II, DQ beta 1
HLA-DRB1	major histocompatibility complex, class II, DR beta 1
MEFV	Mediterranean fever
MIF	macrophage migration inhibitory factor (glycosylation-inhibiting factor)
SAA1	serum amyloid A1
TNF	tumor necrosis factor
TNFRSF1A	tumor necrosis factor receptor superfamily, member 1A