Familial Mediterranean Fever Gene Set

Dataset CTD 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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010505
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1 genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MEFV Mediterranean fever 2.88009