Term Name: spinocerebellar ataxia 46
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the PLD3 gene on chromosome 19q13.
Ontology: Human Disease [DOID:0080288]   ( DOID:0080288 )

Relationships
is a type of: autosomal dominant cerebellar ataxia