Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Abnormal axial muscle morphology +   
Abnormal hyoglossus muscle morphology 
Abnormal lateral cricoarytenoid muscle morphology 
Abnormal mitochondria in muscle tissue  
Abnormal morphology of musculature of pharynx +   
Abnormal morphology of the abdominal musculature +   
Abnormal morphology of the chest musculature 
Abnormal morphology of the musculature of the neck +   
Abnormal morphology of the pelvis musculature +   
Abnormal morphology of the shoulder musculature 
Abnormal muscle fiber morphology +   
Abnormality of facial musculature +   
Abnormality of muscle size +   
Abnormality of musculature of soft palate +  
Abnormality of the back musculature 
Abnormality of the diaphragm +   
Abnormality of the extraocular muscles +   
Abnormality of the musculature of the limbs +   
Abnormality of the musculature of the thorax +   
Abnormality of the tongue muscle +   
Calcification of muscles 
Calcinosis  
Decreased muscle mass  
Fatty replacement of skeletal muscle  
Firm muscles  
Flexion contracture +   
Generalized muscular appearance from birth  
Increased intramuscular fat  
Intramuscular hematoma  
Muscle eosinophilia 
Muscle hemorrhage 
Muscular dystrophy +   
The term dystrophy means abnormal growth. However, muscular dystrophy is used to describe primary myopathies with a genetic basis and a progressive course characterized by progressive skeletal muscle weakness and wasting, defects in muscle proteins, and histological features of muscle fiber degeneration (necrosis) and regeneration. If possible, it is preferred to use other HPO terms to describe the precise phenotypic abnormalities.
Muscular edema  
Myopathy +   
Myositis  
Rhabdomyolysis +   
Skeletal muscle fibrosis  
Skeletal muscle steatosis  

Synonyms
Related Synonyms: MUSCLE BIOPSY SHOWS DYSTROPHIC CHANGES
Alternate IDs: HP:0003544 ;   HP:0003806
Xrefs: MSH:D009136 ;   SNOMEDCT_US:193225000 ;   SNOMEDCT_US:73297009 ;   UMLS:C0026850 ;   UMLS:C1864711
Definition Sources: HPO:probinson, Neuromics:vstraub

paths to the root