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Ontology Browser

Term:
oculopharyngeal muscular dystrophy (DOID:11719)
Annotations: Rat: (5) Mouse: (6) Human: (8) Chinchilla: (6) Bonobo: (5) Dog: (5) Squirrel: (6) Pig: (4)
Parent Terms Term With Siblings Child Terms
Adult-Onset Muscular Dystrophy with Leukoencephalopathy 
Alpha-B Crystallinopathy with Cataract 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Bassoe Syndrome 
Becker muscular dystrophy +   
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
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, Mabry Type 
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries 
Myofibrillar Myopathy, ZASP-Related  
Myopathy with Abnormal Lipid Metabolism  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myotonic disease +   
oculopharyngeal muscular dystrophy +   
An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.
Oculopharyngodistal Myopathy +   
Progressive Muscular Dystrophy, Pectorodorsal 
scapuloperoneal myopathy +   
Vacuolar Neuromyopathy 

Synonyms
Exact Synonyms: OPMD ;   Oculopharyngeal Dystrophy ;   Oculopharyngeal Muscular Dystrophies ;   Progressive Muscular Dystrophy, Oculopharyngeal Type
Primary IDs: MESH:D039141 ;   RDO:0001902
Alternate IDs: OMIM:164300
Xrefs: NCI:C84942
Definition Sources: MESH:D039141

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