Term Name:	spinocerebellar ataxia type 13
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by developmental delay, ataxia, myoclinic jerks, dysarthria, dysphagia and seizure, and has_material_basis_in mutation in the KCNC3 gene.
Ontology:	Human Disease [DOID:0050963]   ( DOID:0050963 )