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Muscular Dystrophy, Oculopharyngeal
Hierarchy: | ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal ∟ ∟ ∟ ∟ ∟ Muscular Dystrophy, Oculopharyngeal |
Annotation: | /vet: coord with MUSCULAR DYSTROPHY, ANIMAL
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History note: | Muscular Dystrophies (1969-2002)X |
historyNote*: | 2003; use MUSCULAR DYSTROPHIES 2001-2002
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publicMeSHNote*: | 2003; see MUSCULAR DYSTROPHIES 2001-2002
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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.
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activeMeSHYear*: | |
dateCreated*: | 2002-07-03X |
dateEstablished*: | 2003-01-01X |
dateRevised*: | 2004-07-29X |
recordAuthorizer*: | jlsX |
recordMaintainer*: | jlsX |
recordOriginator*: | jmpX |
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Labels and equivalent concepts: | Okulofaryngeaalinen dystrofia (fi) XOkulofaryngeaalinen lihasdystrofia (fi, replaced) Lihasdystrofia okulofaryngeaalinen (fi, replaced) Muskeldystrofi, okulofaryngeal (sv) Dystrophia musculorum oculopharyngealis (la-FI, replaced) |
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