BabelNet

bn:16604316n

Noun Concept

No term available

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

zeldzame ziekte

Spinocerebellaire ataxie

GENETIC ASSOCIATION

CACNA1A

HEALTH SPECIALTY

neurologie