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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Joint Diseases +     
muscular disease +     
ankylosis +   
Arthralgia +   
arthritis +   
Arthrogryposis +   
arthropathy +   
atrophic muscular disease +   
Autoimmune Interstitial Lung, Joint, and Kidney Disease  
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Brachydactylous Dwarfism Mseleni Type 
bursitis +  
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome  
Chondromatosis, Synovial +  
chronic fatigue syndrome  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint.
Coracoclavicular Joint, Anomalous 
Craniomandibular Disorders +   
Crystal Arthropathies +   
diaphragm disease +   
Dimauro Disease  
Dwarfism Stiff Joint Ocular Abnormalities 
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 +   
Femoracetabular Impingement 
fibromyalgia +   
Fingerprint Body Myopathy 
Flynn Aird Syndrome 
Frank-Ter Haar syndrome  
Gamstorp-Wohlfart syndrome  
Hallux Limitus 
Hallux Rigidus 
hemarthrosis +   
hereditary arterial and articular multiple calcification syndrome +   
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hydrarthrosis 
hypermobility syndrome 
Hypertrophia Musculorum Vera 
Internal Anal Sphincter Myopathy 
Joint Deformities, Acquired 
Joint Instability +   
Joint Loose Bodies 
Kocher-Debre-Semelaigne Syndrome 
Laplane Fontaine Lagardere Syndrome 
Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy  
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leri Pleonosteosis 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Metatarsalgia +  
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Morillo-Cucci Passarge Syndrome 
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 
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
Myotoxicity 
nail-patella syndrome +   
neurogenic arthropathy +   
neutral lipid storage disease +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
patellofemoral pain syndrome 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Pfeiffer Palm Teller Syndrome 
Plica syndrome 
primary hypertrophic osteoarthropathy +   
progressive pseudorheumatoid arthropathy of childhood  
Proximal Myopathy with Focal Depletion of Mitochondria 
proximal symphalangism +   
Rhabdomyolysis +   
secondary hypertrophic osteoarthropathy  
Short Stature and Locking Fingers 
shoulder impingement syndrome 
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
synovitis +   
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
Temporomandibular Joint Disorders +   
tendinitis +   
Thai Symphalangism Syndrome 
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  
Weill-Marchesani Syndrome 2  

Synonyms
Exact Synonyms: Contractures
Primary IDs: MESH:D003286 ;   RDO:0000395
Definition Sources: MESH:D003286

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