Term Name: spinocerebellar ataxia type 18
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23.
Ontology: Human Disease [DOID:0050969]   ( DOID:0050969 )

Relationships
is a type of: autosomal dominant cerebellar ataxia