Disease association ontology term - MONDO:0011781 - spinocerebellar ataxia type 17

Term summary

ID

MONDO:0011781

Name

spinocerebellar ataxia type 17

Ontology or CV name

Disease association

Definition

A rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.

Parents

• is_a cerebelloparenchymal disorder
• is_a Huntington disease-like syndrome
• is_a autosomal dominant cerebellar ataxia type I

Annotation