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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Hypertrophy +     
muscle tissue disease +     
3-methylcrotonyl-CoA carboxylase deficiency +   
atrophic muscular disease +   
Cardiomegaly +   
cysticercosis +  
distal arthrogryposis +   
epidemic pleurodynia 
gas gangrene  
Gigantomastia 
Hepatomegaly +   
Hypertrophia Musculorum Vera 
Hypertrophy of Masticatory Muscles 
Kocher-Debre-Semelaigne Syndrome 
malignant hyperthermia +   
Muscle Tissue Neoplasms +   
myopathy +   
myostatin-related muscle hypertrophy  
A muscle tissue disease characterized by increased muscle bulk and strength that has_material_basis_in homozygous mutation in the MSTN gene on chromosome 2q32.2. (DO)
rippling muscle disease 1  
sinoatrial node disease +   
Splenomegaly +   
toxocariasis +   

Synonyms
Exact Synonyms: MSLHP ;   muscle hypertrophy syndrome
Primary IDs: MESH:C536106
Alternate IDs: MIM:614160
Xrefs: GARD:10238 ;   ORDO:275534
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/15215484 "DO" "DO"

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