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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
muscle tissue disease +     
3-methylcrotonyl-CoA carboxylase deficiency +   
atrophic muscular disease +   
A neuromuscular disease that is characterized by an abnormal reduction in the muscle volume and atrophy. (DO)
cysticercosis +  
distal arthrogryposis +   
epidemic pleurodynia 
gas gangrene  
malignant hyperthermia +   
Muscle Tissue Neoplasms +   
myopathy +   
myostatin-related muscle hypertrophy  
rippling muscle disease 1  
sinoatrial node disease +   
toxocariasis +   

Synonyms
Exact Synonyms: atrophic muscular disorder ;   atrophic muscular disorders ;   disuse atrophies ;   disuse atrophy ;   spinobulbar atrophies ;   spinobulbar atrophy ;   spinopontine atrophies ;   spinopontine atrophy
Narrow Synonyms: distal lower limb amyotrophy
Primary IDs: MESH:D020966
Xrefs: EFO:0009912 ;   NCI:C84574
Definition Sources: https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&version=14.10d&code=C84574 "DO" "DO"

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