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bn:16604316n
Noun Concept
SYL
No term available
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
Relations
Sources
IS A
EN
rare disease
EN
spinocerebellar ataxia
GENETIC ASSOCIATION
EN
Cav2.1
HEALTH SPECIALTY
EN
neurology

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