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- Q3026441 subject Q6853484.
- Q3026441 subject Q7013290.
- Q3026441 subject Q7022918.
- Q3026441 subject Q7157648.
- Q3026441 abstract "Machado–Joseph disease (MJD), also known as Machado–Joseph Azorean disease or Joseph's disease or Spinocerebellar ataxia type 3 (SCA3), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, which results in a lack of muscle control and coordination of the upper and lower extremities. The symptoms are caused by a genetic mutation that results in an expansion of abnormal "CAG" trinucleotide repeats in the ATXN3 gene that results in an abnormal form of the protein ataxin which causes degeneration of cells in the hindbrain. Some symptoms, such as clumsiness and rigidity, make MJD commonly mistaken for drunkenness and/or Parkinson's disease.Machado–Joseph disease is a type of spinocerebellar ataxia and is the most common cause of autosomal-dominant ataxia. MJD causes ophthalmoplegia and mixed sensory and cerebellar ataxia.".
- Q3026441 icd10 "G11.1".
- Q3026441 icd9 "334.2".
- Q3026441 meshId "D017827".
- Q3026441 omim "109150".
- Q3026441 wikiPageExternalLink machado-joseph-disease.
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- Q3026441 wikiPageWikiLink Q6853484.
- Q3026441 wikiPageWikiLink Q6887300.
- Q3026441 wikiPageWikiLink Q7013290.
- Q3026441 wikiPageWikiLink Q7022918.
- Q3026441 wikiPageWikiLink Q7157648.
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- Q3026441 icd "334.2".
- Q3026441 icd "G11.1".
- Q3026441 meshid "D017827".
- Q3026441 name "Machado-Joseph disease".
- Q3026441 omim "109150".
- Q3026441 type Disease.
- Q3026441 type Thing.
- Q3026441 type Q12136.
- Q3026441 comment "Machado–Joseph disease (MJD), also known as Machado–Joseph Azorean disease or Joseph's disease or Spinocerebellar ataxia type 3 (SCA3), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, which results in a lack of muscle control and coordination of the upper and lower extremities.".
- Q3026441 label "Machado–Joseph disease".
- Q3026441 name "Machado-Joseph disease".