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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
muscular dystrophy +     
Adult-Onset Muscular Dystrophy with Leukoencephalopathy  
Alpha-B Crystallinopathy with Cataract 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
autosomal recessive distal hereditary motor neuronopathy 7  
Bassoe Syndrome 
Becker muscular dystrophy  
congenital muscular dystrophy +   
distal myopathy +   
A muscular dystrophy that is characterized by predominant weakness and atrophy beginning in the feet and/or hands. (DO)
Duchenne muscular dystrophy +   
Emery-Dreifuss muscular dystrophy +   
facioscapulohumeral muscular dystrophy +   
glycogen storage disease VII  
limb-girdle muscular dystrophy +   
Muscular Dystrophy, Animal +   
Muscular Dystrophy, Barnes Type 
Muscular Dystrophy, Cardiac Type 
MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME  
Muscular Dystrophy, Mabry Type 
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries 
Myofibrillar Myopathy, ZASP-Related  
Myopathy with Abnormal Lipid Metabolism  
myotonic disease +   
oculopharyngeal muscular dystrophy +   
Oculopharyngeal Muscular Dystrophy 2  
oculopharyngodistal myopathy +   
Progressive Muscular Dystrophy, Pectorodorsal 
Scapulohumeroperoneal Myopathy  
Vacuolar Neuromyopathy  

Synonyms
Exact Synonyms: distal muscle weakness ;   distal muscular dystrophies ;   distal muscular dystrophy ;   distal myopathy, Markesbery Griggs type ;   distal myopathy, early-onset, autosomal dominant ;   distal myopathy, late hereditary
Primary IDs: MESH:D049310
Xrefs: ICD10CM:G71.09 ;   MIM:PS160500 ;   NCI:C84675 ;   ORDO:399086 ;   ORDO:399096 ;   ORDO:5448 ;   ORDO:63273
Definition Sources: https://rarediseases.org/rare-diseases/distal-myopathy/ "DO" "DO"

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