Term Name: spinocerebellar ataxia type 30
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene.
Ontology: Human Disease [DOID:0050979]   ( DOID:0050979 )

Relationships
is a type of: autosomal dominant cerebellar ataxia