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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Brody myopathy  
A neuromuscular disease is characterized by difficulty relaxing muscles and muscle stiffness following exercise or other strenuous activity and is located_in skeletal muscles.
Charcot-Marie-Tooth disease X-linked recessive 5  
Congenital Myopathy with Fast-Twitch (Type ii) Fiber Atrophy  
muscular dystrophy +   
Myotonia Congenita, Autosomal Dominant  
Myotonia Congenita, Autosomal Recessive  
Myotonia with Skeletal Abnormalities and Mental Retardation 
Native American myopathy  
postpoliomyelitis syndrome 
Potassium Aggravated Myotonia  

Synonyms
Exact Synonyms: Brody disease ;   autosomal recessive Brody myopathy
Primary IDs: MESH:C536607
Alternate IDs: OMIM:601003 ;   RDO:0002237
Xrefs: GARD:9158
Definition Sources: https://ghr.nlm.nih.gov/condition/brody-myopathy "DO", https://rarediseases.info.nih.gov/gard/9158/brody-myopathy/case/23360/case-questions "DO"

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