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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Mitochondrial Cytopathy +     
myopathy +     
Alcohol Myopathy  
centronuclear myopathy +   
congenital myopathy +   
congenital structural myopathy +   
Kearns-Sayre syndrome  
King Denborough syndrome  
mitochondrial myopathy +   
A myopathy that is characterized by mitochondrial dysfunction. (DO)
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
Myoectodermal Gonadal Dysgenesis Syndrome  
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 with Myalgia, increased Serum Creatine Kinase, and with or without Episodic Rhabdomyolysis  
Myopathy, Cataract, Hypogonadism Syndrome 
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
myositis +   
Myostitis 
neurogenic scapuloperoneal syndrome Kaeser type  
Neutral Lipid Storage Disease with Myopathy  
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
polymyalgia rheumatica  
Reducing Body Myopathies +   
rhabdomyolysis-myalgia syndrome 
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" "DO", http://www.ninds.nih.gov/disorders/mitochondrial_myopathy/mitochondrial_myopathy.htm "DO" "DO"

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