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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Muscular Diseases (D009135)
Parent Node: Rheumatic Diseases (D012216)
..Starting node ..Fibromyalgia (D005356)
Child Nodes:
Sister Nodes:
..Acute rheumatism (C538407)
..Arthritis, Juvenile (D001171) 3
..Arthritis, Rheumatoid (D001172) 9
..Fibromyalgia (D005356)
..Gout (D006073) 6
..Hyperostosis, Sternocostoclavicular (D015218)
..Osteoarthritis (D010003) 8
..Polymyalgia Rheumatica (D011111)
..Rheumatic Fever (D012213) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4289
Name:	Fibromyalgia
Definition:	A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95)
Alternative IDs:
ParentIDs:	MESH:D009135\|MESH:D012216
TreeNumbers:	C05.651.324 \|C05.799.321 \|C10.668.491.425
Synonyms:	Diffuse Myofascial Pain Syndrome \|Fibromyalgia Fibromyositis Syndrome \|Fibromyalgia-Fibromyositis Syndrome \|Fibromyalgia-Fibromyositis Syndromes \|Fibromyalgia, Primary \|Fibromyalgias \|Fibromyalgia, Secondary \|Fibromyalgias, Primary \|Fibromyalgias, Secondary \|Fibr
Slim Mappings:	Musculoskeletal disease\|Nervous system disease
Reference:	MedGen: D005356 MeSH: D005356 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants