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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
myopathy +     
Rhabdomyolysis +     
Alcohol Myopathy  
centronuclear myopathy +   
congenital myopathy +   
congenital structural myopathy +   
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
King Denborough syndrome  
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
myofascial pain syndrome +   
myofibrillar myopathy +   
myoglobinuria +   
A myopathy that is characterized by an increased urinary excretion of myoglobin. (DO)
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  
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
polymyalgia rheumatica  
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Recurrent Metabolic Encephalomyopathic Crises with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration  
Reducing Body Myopathies +   
Rhabdomyolysis, Cerivastatin-Induced  
rhabdomyolysis-myalgia syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Tubular Aggregate Myopathies +   
X-linked myopathy with excessive autophagy