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Ontology Browser

Parent Terms Term With Siblings Child Terms
myopathy +     
Alcohol Myopathy  
Brody myopathy  
centronuclear myopathy +   
Charcot-Marie-Tooth disease X-linked recessive 5  
congenital myopathy +   
Congenital Myopathy with Fast-Twitch (Type ii) Fiber Atrophy  
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 +   
A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
myofascial pain syndrome +   
myofibrillar myopathy +   
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  
myositis +   
neurogenic scapuloperoneal syndrome Kaeser type  
Neutral Lipid Storage Disease with Myopathy  
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
polymyalgia rheumatica  
postpoliomyelitis syndrome 
Reducing Body Myopathies +   
rhabdomyolysis-myalgia syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Tubular Aggregate Myopathies +   
X-linked myopathy with excessive autophagy  

Exact Synonyms: Myodystrophica ;   muscular dystrophies ;   myodystrophicas ;   myodystrophies ;   myodystrophy
Primary IDs: MESH:D009136
Alternate IDs: RDO:0000546
Xrefs: GARD:7922 ;   NCI:C84910
Definition Sources: "DO" "DO", "DO" "DO", MESH:D009136

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