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Olivopontocerebellar Atrophies
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies 15 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ ∟ Olivopontocerebellar Atrophies ∟ ∟ ∟ Olivopontocerebellar Atrophies |
Annotation: | DF: OPCA
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History note: | Atrophy (1966-1986) | Brain Diseases (1966-1986) | Cerebellar Ataxia (1968-1986) | Cerebellar Diseases (1966-1986) | Olivary Nucleus (1966-1986) | Pons (1966-1986)X |
historyNote*: | 2000(1987)
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publicMeSHNote*: | 2000; see OLIVOPONTOCEREBELLAR ATROPHY 1991-1999, see SPINOCEREBELLAR DEGENERATION 1987-1990
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Scope note: | A group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)
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activeMeSHYear*: | |
dateCreated*: | 1986-03-31X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2005-07-21X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | RCX |
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Labels and equivalent concepts: | Olivopontoserebellaariset degeneraatiot (fi) XOlivopontoserebellaariset atrofiat (fi, replaced) Olivopontoserebellaarinen degeneraatio (fi, replaced) Olivopontoserebellaarinen atrofia (fi, replaced) Presenil ataxi (sv, replaced) Dejerine-Thomas syndrom (sv, replaced) Presenile Ataxia (en, replaced) Olivo-Ponto-Cerebellar Atrophy (en, replaced) Inherited Olivopontocerebellar Atrophy (en, replaced) Olivo-Ponto-Cerebellar Degeneration (en, replaced) Olivopontocerebellar Atrophy (en, replaced) Pontoolivocerebellar Atrophy (en, replaced) Olivopontocerebellar Degeneration (en, replaced) Dejerine-Thomas Syndrome (en, replaced) Atrophia olivopontocerebellaris (la-FI, replaced) Degeneratio olivopontocerebellaris (la-FI, replaced) |
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