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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
myopathy +     
Alcohol Myopathy  
Brody myopathy  
centronuclear myopathy +   
Charcot-Marie-Tooth disease X-linked recessive 5  
congenital myopathy +   
Congenital Myopathy with Fast-Twitch (Type ii) Fiber Atrophy  
congenital structural myopathy +   
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
myofascial pain syndrome +   
myofibrillar myopathy +   
myoglobinuria +   
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, Cataract, Hypogonadism Syndrome 
myopathy, lactic acidosis, and sideroblastic anemia +   
myositis +   
Myostitis 
polymyalgia rheumatica  
postpoliomyelitis syndrome 
reducing body myopathy +   
Secretory Diarrhea, Myopathy, and Deafness 
spheroid body myopathy  
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: Myodystrophica ;   muscular dystrophies ;   myodystrophicas ;   myodystrophies ;   myodystrophy
Primary IDs: MESH:D009136
Alternate IDs: RDO:0000546
Xrefs: GARD:7922 ;   NCI:C84910
Definition Sources: MESH:D009136, http://en.wikipedia.org/wiki/Muscular_dystrophy, http://www.ninds.nih.gov/disorders/md/md.htm

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