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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  
mitochondrial myopathy +   
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, CONGENITAL, PROGRESSIVE, WITH SCOLIOSIS  
myopathy, lactic acidosis, and sideroblastic anemia +   
myositis +   
Myostitis 
polymyalgia rheumatica  
reducing body myopathy +   
Secretory Diarrhea, Myopathy, and Deafness 
spheroid body myopathy  
X-linked myopathy with excessive autophagy  

Synonyms
Primary IDs: RDO:9003969

paths to the root

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