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Summary Literature (0)
DOID:0060162 - dentatorubral-pallidoluysian atrophy

Disease Ontology 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.

Synonyms: DRPLA; Haw River Syndrome; Naito-Oyanagi disease

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : atn1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant cerebellar ataxia (is_a)

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