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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
muscular disease +     
myopathy +     
Alcohol Myopathy  
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  
centronuclear myopathy +   
chronic fatigue syndrome  
compartment syndrome +   
congenital myopathy +   
Congenital Myopathy with Neuropathy and Deafness  
congenital structural myopathy +   
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 periodic paralysis +   
fibromyalgia +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hypertrophia Musculorum Vera 
Internal Anal Sphincter Myopathy 
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
muscular atrophy +   
muscular dystrophy +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
myofibrillar myopathy +   
myoglobinuria +   
Myopathic Carnitine Deficiency 
Myopathy due to Malate-Aspartate Shuttle Defect 
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  
myopathy of extraocular muscle +   
myopathy with extrapyramidal signs  
Myopathy with Giant Abnormal Mitochondria 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Cataract, Hypogonadism Syndrome 
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
Inflammation of a muscle or muscle tissue.
myostatin-related muscle hypertrophy  
Myostitis 
myotonic disease +   
Myotoxicity 
neurogenic scapuloperoneal syndrome Kaeser type  
neutral lipid storage disease +   
Neutral Lipid Storage Disease with Myopathy  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polymyalgia rheumatica  
Proximal Myopathy with Focal Depletion of Mitochondria 
Reducing Body Myopathies +   
Rhabdomyolysis +   
Secretory Diarrhea, Myopathy, and Deafness 
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Tubular Aggregate Myopathies +   
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: Focal Myositides ;   Focal Myositis ;   Idiopathic Inflammatory Myopathies ;   Idiopathic Inflammatory Myopathy ;   Idiopathic Inflammatory Myositis ;   Infectious Myositides ;   Infectious Myositis ;   Inflammatory Muscle Disease ;   Inflammatory Muscle Diseases ;   Inflammatory Myopathies ;   Inflammatory Myopathy ;   Inflammatory disorder of muscle ;   Myositides ;   Proliferative Myositides ;   Proliferative Myositis
Primary IDs: MESH:D009220 ;   RDO:0003679
Xrefs: ICD10CM:M60 ;   ICD10CM:M60.9 ;   NCI:C27578
Definition Sources: http://www.nlm.nih.gov/medlineplus/myositis.html "DO", https://en.wikipedia.org/wiki/Myositis "DO", MESH:D009220

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