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- Q9386865 subject Q6902120.
- Q9386865 abstract "Olivopontocerebellar atrophy (OPCA) is the degeneration of neurons in specific areas of the brain – the cerebellum, pons, and inferior olives. OPCA is present in several neurodegenerative syndromes, including inherited and non-inherited forms of ataxia (such as the hereditary spinocerebellar ataxia known as Machado–Joseph disease) and multiple system atrophy (MSA), with which it is primarily associated.OPCA may also be found in the brains of individuals with prion disorders and inherited metabolic diseases. The characteristic areas of brain damage that indicate OPCA can be seen by imaging the brain using CT scans or MRI studies.The term was originally coined by Joseph Jules Dejerine and André Thomas.".
- Q9386865 icd10 "G23.8".
- Q9386865 icd9 "333.0".
- Q9386865 meshId "D009849".
- Q9386865 thumbnail Gray707.png?width=300.
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- Q9386865 wikiPageWikiLink Q6902120.
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- Q9386865 icd "333".
- Q9386865 icd "G23.8".
- Q9386865 meshid "D009849".
- Q9386865 name "Olivopontocerebellar atrophy".
- Q9386865 type Disease.
- Q9386865 type Thing.
- Q9386865 type Q12136.
- Q9386865 comment "Olivopontocerebellar atrophy (OPCA) is the degeneration of neurons in specific areas of the brain – the cerebellum, pons, and inferior olives.".
- Q9386865 label "Olivopontocerebellar atrophy".
- Q9386865 depiction Gray707.png.
- Q9386865 name "Olivopontocerebellar atrophy".