familial mediterranean fever Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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

2 genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
MEFV Mediterranean fever
SAA1 serum amyloid A1