Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
arthropathy +   
autoimmune disease of musculoskeletal system +   
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME  
bone disease +   
cartilage disease +   
Charcot-Marie-Tooth disease +   
chronic fatigue syndrome  
Congenital Hypomyelinating Neuropathy +   
connective tissue disease +   
Cyclic Vomiting Syndrome with Neuromuscular Disease 
Cyprus Facial Neuromusculoskeletal Syndrome 
fasciitis +   
Foot Deformities +   
Foot Diseases +   
GSD IV, Neuromuscular Form, Adult, with Isolated Myopathy 
GSD IV, Neuromuscular Form, Childhood  
GSD IV, Neuromuscular Form, Congenital  
GSD IV, Neuromuscular Form, Fatal Perinatal  
Hand Deformities +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH MUSCLE TONE ABNORMALITIES AND DISTAL SKELETAL DEFECTS  
Jaw Diseases +   
locked-in syndrome 
MORIMOTO-RYU-MALICDAN NEUROMUSCULAR SYNDROME  
motor neuron disease +   
muscular disease +   
A musculoskeletal system disease that affects the muscles. (DO)
Musculoskeletal Abnormalities +   
musculoskeletal system cancer +   
NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES  
neuromuscular disease +   
neuromuscular junction disease +   
Neuromuscular Oculoauditory Syndrome  
 arthrogryposis multiplex congenita +   
 Axial Myopathy, Late-Onset +   
 Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
 Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
 Carey-Fineman-Ziter syndrome +   
 Chanarin-Dorfman syndrome +   
 chronic fatigue syndrome  
 compartment syndrome +   
 Congenital Myopathy with Neuropathy and Deafness  
 Congenital Universal Muscular Hypoplasia of Krabbe 
 Contracture +   
 Craniomandibular Disorders +   
 diaphragm disease +   
 Dimauro Disease  
 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  
 Granulovacuolar Lobular Myopathy with Electrical Myotonia 
 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 +   
 Muscle Cramp +   
 Muscle Rigidity +   
 Muscle Spasticity +   
 muscle tissue disease +   
 Muscle Weakness +   
 Musculoskeletal Pain +   
 Myalgia +   
 myofascial pain syndrome +   
 Myopathic Carnitine Deficiency 
 Myopathy with Lactic Acidosis, Hereditary  
 myotonic disease +   
 Myotoxicity 
 Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
 Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
 Pectoralis Muscle, Absence of 
 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
 Proximal Myopathy with Focal Depletion of Mitochondria 
 Rhabdomyolysis +   
 Singleton Merten Syndrome +   
 Skeletal Muscle Injuries  
 Skeletal Muscle Reperfusion Injury  
 systemic primary carnitine deficiency disease  
 Tel Hashomer Camptodactyly Syndrome 
 tendinitis +   
 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: muscle disorder ;   muscle disorders ;   muscular diseases
Narrow Synonyms: SKELETAL MUSCLE DISEASE
Primary IDs: MESH:D009135
Xrefs: EFO:0002970
Definition Sources: http://www.nlm.nih.gov/medlineplus/muscledisorders.html "DO" "DO"

paths to the root