Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Parent Terms Term With Siblings Child Terms
myopathy +     
Actin-Accumulation Myopathy 
Alcohol Myopathy  
autosomal recessive centronuclear myopathy +   
Cap Myopathy +  
central core myopathy +   
centronuclear myopathy +   
centronuclear myopathy 1  
centronuclear myopathy 2  
centronuclear myopathy 4  
centronuclear myopathy X-linked  
congenital fiber-type disproportion +   
congenital myopathy +   
congenital structural myopathy +   
distal muscular dystrophy Tateyama type  
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
Minicore Myopathy with External Ophthalmoplegia  
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
myofascial pain syndrome +   
myofibrillar myopathy +   
A myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles. (DO)
myoglobinuria +   
Myopathy due to Malate-Aspartate Shuttle Defect 
myopathy of extraocular muscle +   
myopathy with extrapyramidal signs  
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
myopathy, lactic acidosis, and sideroblastic anemia +   
Myosclerosis, Autosomal Recessive  
myositis +   
Myotubular Myopathy with Abnormal Genital Development 
nemaline myopathy +   
Pleoconial Myopathy with Salt Craving 
polymyalgia rheumatica  
reducing body myopathy +   
Secretory Diarrhea, Myopathy, and Deafness 
spheroid body myopathy  
X-linked myopathy with excessive autophagy  

Exact Synonyms: myofibrillar myopathies
Narrow Synonyms: myofibrillar myopathy, dominant
Primary IDs: MESH:C580316
Alternate IDs: DOID:9007578 ;   RDO:0015910
Xrefs: GARD:10529 ;   OMIM:PS601419
Definition Sources:,,

paths to the root


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