Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Joint Diseases +     
muscular disease +     
Absent Patella 
acromesomelic dysplasia, Grebe type  
Anal Sphincter Myopathy, Internal 
ankylosis +   
Antecubital Pterygium 
Arthralgia +   
arthritis +   
Arthrogryposis +   
Persistent flexure or contracture of a joint. 
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 +  
Calcification of Joints and Arteries +   
campomelic dysplasia +   
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome  
Cervical Rib Syndrome +  
Chondromatosis, Synovial +  
chronic fatigue syndrome  
CLOVES syndrome  
Cohen-Gibson Syndrome  
compartment syndrome +   
Congenital Absence of Gluteal Muscles 
Congenital Absence of the Sternocleidomastoid Muscle 
Congenital Hip Dislocation +   
Congenital Limb Deformities +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Coracoclavicular Joint, Anomalous 
Craniofacial Abnormalities +   
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 
Funnel Chest +   
Gamstorp-Wohlfart syndrome  
gastroschisis +   
GEMSS Syndrome  
Hajdu-Cheney syndrome  
Hallux Limitus 
Hallux Rigidus 
hemarthrosis +   
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hip Dysplasia, Beukes Type  
hydrarthrosis 
hypermobility syndrome 
Hypertrophia Musculorum Vera 
IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES  
Joint Deformities, Acquired 
Joint Instability +   
Joint Loose Bodies 
Kleefstra Syndrome 2  
Klippel-Feil syndrome +   
Kocher-Debre-Semelaigne Syndrome 
Laplane Fontaine Lagardere Syndrome 
Laryngomalacia +  
Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy  
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leri Pleonosteosis 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Metatarsalgia +  
MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES  
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 +   
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
Myopathy, Hyaline Body, Autosomal Recessive  
Myopathy, Myosin Storage  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
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 
Pectus Carinatum  
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Pfeiffer Palm Teller Syndrome 
Plica syndrome 
polymyalgia rheumatica  
primary hypertrophic osteoarthropathy +   
progressive pseudorheumatoid arthropathy of childhood  
Proximal Myopathy with Focal Depletion of Mitochondria 
proximal symphalangism  
Pseudoarthrogryposis 
Rhabdomyolysis +   
Sacral Agenesis with Vertebral Anomalies  
Sacrococcygeal Dysgenesis Association 
secondary hypertrophic osteoarthropathy 
Short Stature and Locking Fingers 
SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES  
shoulder impingement syndrome 
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Steel Syndrome  
Sternal Cleft 
synostosis +   
synovitis +   
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
Temporomandibular Joint Disorders +   
tendinitis +   
Ter Haar Syndrome  
Thai Symphalangism Syndrome 
Tracheobronchomalacia +   
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  
Widow's Peak Syndrome 
ZTTK Syndrome  
 Bruck syndrome +   

Synonyms
Exact Synonyms: Arthrogryposes ;   Arthrogryposis Multiplex Congenita ;   Arthrogryposis Multiplex Congenita (AMC) ;   Congenital Arthromyodysplasia ;   Congenital Arthromyodysplasias ;   Congenital Multiple Arthrogryposes ;   Congenital Multiple Arthrogryposis ;   Fibrous Ankylosis of Multiple Joints ;   Guerin Stern Syndrome ;   Guérin Stern Syndrome ;   Myodystrophia Fetalis Deformans ;   Otto Syndrome ;   Rocher Sheldon Syndrome ;   Rossi syndrome ;   amyoplasia congenita
Primary IDs: MESH:D001176
Alternate IDs: RDO:0000318
Definition Sources: MESH:D001176

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