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DeCS
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Descriptor English:
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Muscular Dystrophy, Oculopharyngeal
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Descriptor Spanish:
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Distrofia Muscular Oculofaríngea
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Descriptor Portuguese:
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Distrofia Muscular Oculofaríngea
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Synonyms English:
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Dystrophies, Oculopharyngeal Muscular
Dystrophy, Oculopharyngeal Muscular
Muscular Dystrophies, Oculopharyngeal
Oculopharyngeal Dystrophy
Oculopharyngeal Muscular Dystrophies
Oculopharyngeal Muscular Dystrophy
Progressive Muscular Dystrophy, Oculopharyngeal Type
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Tree Number:
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C05.651.534.500.450
C10.668.491.175.500.450
C16.320.577.450
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Definition English:
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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. |
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Indexing Annotation English:
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/vet: coord with MUSCULAR DYSTROPHY, ANIMAL
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See Related English:
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Poly(A)-Binding Protein II
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History Note English:
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2003; use MUSCULAR DYSTROPHIES 2001-2002
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Allowable Qualifiers English:
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Record Number:
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37274
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Unique Identifier:
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D039141
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Occurrence in VHL:
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Similar:
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DeCS
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