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bn:16604316n
Noun Concept
Categories: Channelopathies, Neurological disorders, Trinucleotide repeat disorders, All articles with unsourced statements, Rare diseases
EN
spinocerebellar ataxia type 6  Episodic and progressive ataxia  SCA6  Spinocerebellar ataxia 6  SPINOCEREBELLAR ATAXIA 6; SCA6
EN
Spinocerebellar ataxia type 6 is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Wikipedia
Definitions
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EN
Spinocerebellar ataxia type 6 is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Wikipedia
A rare, late-onset, autosomal dominant disorder Wikipedia Disambiguation
Human disease Wikidata
IS A
rare disease
spinocerebellar ataxia
GENETIC ASSOCIATION
Cav2.1
HEALTH SPECIALTY
neurology
Wikipedia
EN
spinocerebellar ataxia type 6
Wikidata
EN
spinocerebellar ataxia type 6
Wikipedia Redirections
EN
Episodic and progressive ataxia, SCA6, spinocerebellar ataxia type-6
Wikidata Alias
EN
SCA6, Spinocerebellar ataxia 6, SPINOCEREBELLAR ATAXIA 6; SCA6, Spinocerebellar Ataxia type 6

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