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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
muscular disease +     
myositis +     
rheumatic disease +     
Acute Rheumatism 
antisynthetase syndrome  
arthrogryposis multiplex congenita +   
atrophic muscular disease +   
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  
Congenital Universal Muscular Hypoplasia of Krabbe 
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 syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression. (DO)
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
granulomatous myositis 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hypertrophia Musculorum Vera 
inclusion body myositis +   
Internal Anal Sphincter Myopathy 
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 +   
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
myositis fibrosa 
myositis ossificans  
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 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 ;   Fibromyalgias ;   Fibrositides ;   Fibrositis ;   Muscular Rheumatism ;   Primary Fibromyalgia ;   Primary Fibromyalgias ;   Secondary Fibromyalgia ;   fibromyalgia-fibromyositis syndromes ;   secondary fibromyalgias
Primary IDs: MESH:D005356
Xrefs: ICD10CM:M79.7 ;   NCI:C50566 ;   NCI:C87497
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/30486733/ "DO" "DO", https://pubmed.ncbi.nlm.nih.gov/32120395/ "DO" "DO", https://pubmed.ncbi.nlm.nih.gov/33024295/ "DO" "DO", https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7660651/ "DO" "DO"

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