Fibromyalgia Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores 2025
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

5 genes involed in the disease Fibromyalgia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol	Name	Standardized Value
TAAR1	trace amine associated receptor 1	5.0
COMT	catechol-O-methyltransferase	5.0
HTR2A	5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled	5.0
ADRB2	adrenoceptor beta 2, surface	5.0
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4	5.0