fibromyalgia Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness in the muscles of neck, shoulders, back, hips, arms, and legs. Other signs and symptoms include headaches, fatigue, sleep disturbances, and painful menstruation. (Experimental Factor Ontology, EFO_0005687)
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Genes

6 genes associated with the disease fibromyalgia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
COMT	catechol-O-methyltransferase
HTR2A	5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
SERPINE1	serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC6A3	solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4
TACR1	tachykinin receptor 1