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bn:03685914n
Noun Concept
Categories: Rare diseases, Central nervous system disorders, Channelopathies
EN
spinocerebellar ataxia type 13  Spinocerebellar ataxia type-13  SCA13  SPINOCEREBELLAR ATAXIA 13  SPINOCEREBELLAR ATAXIA 13; SCA13
EN
Spinocerebellar ataxia type 13 is a rare autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, nystagmus, and ataxia of gait, stance and the limbs due to cerebellar dysfunction. Wikipedia
Definitions
Relations
Sources
EN
Spinocerebellar ataxia type 13 is a rare autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, nystagmus, and ataxia of gait, stance and the limbs due to cerebellar dysfunction. Wikipedia
A rare autosomal dominant disorder Wikipedia Disambiguation
Human disease Wikidata
IS A
disease
rare disease
spinocerebellar ataxia
GENETIC ASSOCIATION
KCNC3
HEALTH SPECIALTY
neurology
Wikipedia
EN
Spinocerebellar ataxia type-13
Wikidata
EN
spinocerebellar ataxia type 13
Wikipedia Redirections
EN
SCA13, Spinocerebellar ataxia type 13
Wikidata Alias
EN
SCA13, SPINOCEREBELLAR ATAXIA 13, SPINOCEREBELLAR ATAXIA 13; SCA13, Spinocerebellar Ataxia type 13

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