"MESH:D020191"^^ . "2011-08-29T01:41:48Z"^^ . . . "lschriml"^^ . _:vb50938397 . "DRPLA"@en . "NCI:C122653"^^ . "NCI:C122653"^^ . _:vb50938397 . . "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."^^ . "UMLS_CUI:C0751781"^^ . _:vb50938397 . "Haw River Syndrome"@en . "MESH:D020191"^^ . "UMLS_CUI:C0751781"^^ . "Naito-Oyanagi disease"@en . . "disease_ontology"^^ . _:vb50938397 . "OMIM:125370"^^ . _:vb50938397 . . "dentatorubral-pallidoluysian atrophy"^^ . "GARD:5643"^^ . "DOID:0060162"^^ . "SNOMEDCT_US_2021_09_01:702422004"^^ .