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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
myopathy +     
Alcohol Myopathy  
centronuclear myopathy +   
congenital myopathy +   
congenital structural myopathy +   
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
Kearns-Sayre syndrome  
mitochondrial myopathy +   
A myopathy that is characterized by mitochondrial dysfunction. (DO)
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
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, Epilepsy, and Progressive Cerebral Atrophy  
myositis +   
Myostitis 
neurogenic scapuloperoneal syndrome Kaeser type  
Neutral Lipid Storage Disease with Myopathy  
polymyalgia rheumatica  
Reducing Body Myopathies +   
Secretory Diarrhea, Myopathy, and Deafness 
Tubular Aggregate Myopathies +   
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: Luft disease ;   Luft's Disease ;   Lufts Disease ;   Megaconial Myopathy ;   Mitochondrial Myopathies ;   Pleoconial Myopathies ;   megaconial myopathies ;   pleoconial myopathy
Narrow Synonyms: MITOCHONDRIAL MYOPATHY, ISOLATED ;   MYOPATHY, MITOCHONDRIAL, LATE-ONSET ;   MYOTONIC DYSTROPHY-LIKE MYOPATHY ;   skeletal myopathy, responsive to riboflavin
Primary IDs: MESH:D017240
Alternate IDs: OMIM:251900
Xrefs: NCI:C101328
Definition Sources: http://en.wikipedia.org/wiki/Mitochondrial_myopathies "DO", http://www.ninds.nih.gov/disorders/mitochondrial_myopathy/mitochondrial_myopathy.htm "DO"

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