Term Name:	cerebellar ataxia type 43
Synonyms:	SCA43
Definition:	An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.
Ontology:	Human Disease [DOID:0111745]   ( DOID:0111745 )