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Ontology Browser

Parent Terms Term With Siblings Child Terms
myopathy +     
Actin-Accumulation Myopathy  
Alcohol Myopathy  
autosomal recessive centronuclear myopathy +   
Cap Myopathy +  
central core disease +   
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  
King Denborough syndrome  
mitochondrial myopathy +   
multiminicore disease  
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, Epilepsy, and Progressive Cerebral Atrophy  
Myosclerosis, Autosomal Recessive  
myositis +   
Myotubular Myopathy with Abnormal Genital Development 
nemaline myopathy +   
neurogenic scapuloperoneal syndrome Kaeser type  
Neutral Lipid Storage Disease with Myopathy  
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
Pleoconial Myopathy with Salt Craving 
polymyalgia rheumatica  
Reducing Body Myopathies +   
rhabdomyolysis-myalgia syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Tubular Aggregate Myopathies +   
X-linked myopathy with excessive autophagy  

Exact Synonyms: myofibrillar myopathies
Narrow Synonyms: myofibrillar myopathy, dominant
Primary IDs: MESH:C580316
Xrefs: GARD:10529 ;   NCI:C83009 ;   OMIM:PS601419
Definition Sources: "DO" "DO", "DO" "DO", "DO" "DO"

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