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Ontology Browser

Parent Terms Term With Siblings Child Terms
Acantholysis +  
arthrogryposis multiplex congenita +   
Atrial Remodeling  
atrophic muscular disease +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
bilirubin metabolic disorder +   
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Cardiac Arrhythmias +   
Cardiotoxicity +   
Carey-Fineman-Ziter syndrome  
Channelopathies +   
Chromosome Aberrations +   
chronic fatigue syndrome  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Congenital Universal Muscular Hypoplasia of Krabbe 
Contracture +   
Craniomandibular Disorders +   
Death +   
Delayed Graft Function 
diaphragm disease +   
Dimauro Disease  
Disease Attributes +   
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
Emphysema +   
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
Extravasation of Diagnostic and Therapeutic Materials  
familial periodic paralysis +   
Fasciculation +   
Femoracetabular Impingement 
fibromyalgia +   
Fibrosis +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
Genomic Instability +   
Granuloma +   
Growth Disorders +   
Hemolysis +   
Hemorrhage +   
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Heterotopic Ossification +   
Hyperammonemia +   
Hyperplasia +   
Hypertrophia Musculorum Vera 
hyperuricemia +   
Inflammation +   
Internal Anal Sphincter Myopathy 
Intraoperative Complications +   
ischemia +   
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leukocytosis +   
Long Term Adverse Effects 
Malacoplakia +  
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Menstruation Disturbances +   
Metaplasia +   
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Muscle Cramp +   
Muscle Hypertonia +   
Muscle Hypotonia +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251)
muscular atrophy +   
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myokymia +   
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
Myotonia +   
myotonic disease +   
Necrosis +   
Neoplastic Processes +   
Nerve Degeneration +   
neutral lipid storage disease +   
ochronosis +  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Orofacial Granulomatosis 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
pigmentation disease +   
Polydipsia +   
Postoperative Complications +   
Protein Aggregation, Pathological  
Proximal Myopathy with Focal Depletion of Mitochondria 
Respiratory Aspiration +  
Rhabdomyolysis +   
Sclerosis +   
Shock +   
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Spasm +   
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Ulcer +   
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Myopathy  
Vascular Remodeling +   
very long chain acyl-CoA dehydrogenase deficiency  
Yang Deficiency 
Yin Deficiency 

Exact Synonyms: Muscle Weaknesses ;   Muscular Weakness ;   Muscular Weaknesses
Primary IDs: MESH:D018908 ;   RDO:0002465
Definition Sources: MESH:D018908

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