- Concept UI
- M0335587
- Scope Note
- 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.
- Terms
-
Muscular Dystrophy, Oculopharyngeal
Preferred Term
Term UI
T369181
Date11/08/1999
LexicalTag
NON
ThesaurusID
-
Oculopharyngeal Muscular Dystrophy
Term UI
T812267
Date11/15/2011
LexicalTag
NON
ThesaurusID
-
Oculopharyngeal Dystrophy
Term UI
T842183
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Progressive Muscular Dystrophy, Oculopharyngeal Type
Term UI
T842184
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)