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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
muscular disease +     
myositis +     
Tendon Injuries +     
Anal Sphincter Myopathy, Internal 
Antisynthetase Syndrome  
Arthrogryposis +   
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  
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 +   
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 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 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polymyalgia rheumatica  
Polymyositis +   
Proximal Myopathy with Focal Depletion of Mitochondria 
pyomyositis 
Rhabdomyolysis +   
Rotator Cuff Injuries 
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance.
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  

Synonyms
Exact Synonyms: Tendinitides ;   Tendinopathies ;   Tendinopathy ;   Tendinoses ;   Tendinosis ;   Tendonitides ;   Tendonitis ;   Tendonopathies ;   Tendonopathy ;   Tendonoses ;   Tendonosis
Primary IDs: MESH:D052256 ;   RDO:0006681
Alternate IDs: RDO:9003127
Xrefs: NCI:C97141
Definition Sources: MESH:D052256

paths to the root

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