dentatorubral-pallidoluysian atrophy (DOID:0060162)
Alliance: disease page
Synonyms: DRPLA; Haw River Syndrome; Naito-Oyanagi disease
Alt IDs: OMIM:125370, MESH:D020191, NCI:C122653, UMLS_CUI:C0751781
Definition: An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein.