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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
muscular disease +     
myositis +     
rheumatic disease +     
Acute Rheumatism 
Anal Sphincter Myopathy, Internal 
Antisynthetase Syndrome 
Arthrogryposis +   
atrophic muscular disease +   
autoimmune disease of skin and connective tissue +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome  
chronic fatigue syndrome  
chronic rheumatic pericarditis 
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Craniomandibular Disorders +   
diaphragm disease +   
Dimauro Disease  
Early-Onset Myopathy with Fatal Cardiomyopathy  
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
Familial Idiopathic Inflammatory Myopathy  
familial periodic paralysis +   
fibromyalgia +   
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)
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
granulomatous myositis 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hypertrophia Musculorum Vera 
inclusion body myositis +   
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Macrophagic Myofasciitis 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
myopathy +   
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
MYOPATHY, SCAPULOHUMEROPERONEAL  
myositis +   
myositis fibrosa 
myositis ossificans  
myostatin-related muscle hypertrophy  
myotonic disease +   
Myotoxicity 
neutral lipid storage disease +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Orbital Myositis 
osteoarthritis +   
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polymyalgia rheumatica  
Polymyositis +   
Proximal Myopathy with Focal Depletion of Mitochondria 
pyomyositis 
Rhabdomyolysis +   
rheumatic fever +   
rheumatic pulmonary valve disease 
rheumatoid arthritis +   
scleroderma +   
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Sternocostoclavicular Hyperostosis 
systemic lupus erythematosus +   
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay Faciocardiomusculoskeletal Syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  
 panniculitis +   

Synonyms
Exact Synonyms: Diffuse Myofascial Pain Syndrome ;   Fibromyalgia Fibromyositis Syndrome ;   Fibromyalgia-Fibromyositis Syndromes ;   Fibromyalgias ;   Fibrositides ;   Fibrositis ;   Muscular Rheumatism ;   Primary Fibromyalgia ;   Primary Fibromyalgias ;   Secondary Fibromyalgia ;   Secondary Fibromyalgias
Primary IDs: MESH:D005356 ;   RDO:0005604
Xrefs: ICD10CM:M79.1 ;   ICD10CM:M79.7 ;   NCI:C50566 ;   NCI:C87497
Definition Sources: MESH:D005356

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.