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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 +   
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 +   
A myopathy that is characterized by progressive external ocular, facial and pharyngeal muscle weakness, leading to variable degrees of ptosis, ophthalmoparesis, facial muscle atrophy, dysarthria and dysphagia, as well as distal muscle weakness and atrophy of lower and upper extremities. (DO)
Progressive Muscular Dystrophy, Pectorodorsal 
Scapulohumeroperoneal Myopathy  
Vacuolar Neuromyopathy  

Synonyms
Exact Synonyms: FOLP-DR ;   OPDM ;   faciooculolaryngopharyngeal myopathy with distal and respiratory involvement ;   oculopharyngodistal myopathies
Primary IDs: MESH:C563508
Alternate IDs: DOID:9008215
Xrefs: GARD:12592 ;   OMIM:PS164310 ;   ORDO:98897
Definition Sources: https://jnnp.bmj.com/content/75/10/1499 "DO" "DO"

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