Machado-Joseph disease (Q3026441)
Jump to navigation
Jump to search
autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has material basis in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene
- Azorean disease (disorder)
- MJD
- spinocerebellar ataxia type 3
- spinocerebellar ataxia 3
- Azorean disease
- Nigrospinodentatal Degeneration
- MACHADO-JOSEPH DISEASE; MJD
- Autosomal dominant striatonigral degeneration
- Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia
- Spinopontine Atrophy
- Spinocerebellar Atrophy 3
- Machado disease
- Azorean Neurologic Disease
- Azorean disease of the nervous system
- SCA3
- MACHADO-JOSEPH DISEASE
Language | Label | Description | Also known as |
---|---|---|---|
English | Machado-Joseph disease |
autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has material basis in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene |
|
Statements
1 reference
1 reference
1 reference
1 reference
336.8
1 reference
Identifiers
Machado-Joseph Disease
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(11 entries)
- arwiki مرض ماتشادو جوزيف
- bswiki Machado-Josephova bolest
- cawiki Malaltia de Machado-Joseph
- enwiki Machado–Joseph disease
- eswiki Enfermedad de Machado-Joseph
- frwiki Maladie de Machado-Joseph
- hewiki מחלת משאדו-ז'וזף
- jawiki マチャド・ジョセフ病
- ptwiki Doença de Machado-Joseph
- ruwiki Болезнь Мачадо-Джозефа
- svwiki Machado-Josephs sjukdom