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Disease association ontology term - MONDO:0013594 - spinocerebellar ataxia type 36

Term summary

ID
MONDO:0013594
Name
spinocerebellar ataxia type 36
Ontology or CV name
Disease association
Definition
Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.

Parents

Annotation

Disease association

MONDO:0013594 - spinocerebellar ataxia type 36

References:

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