Search Ontology:
Human Disease

dentatorubral-pallidoluysian atrophy

Term ID
DOID:0060162
Synonyms
  • DRPLA
  • Haw River Syndrome
  • Naito-Oyanagi disease
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. http://en.wikipedia.org/wiki/Dentatorubral-pallidoluysian_atrophy
References
Ontology
Human Disease   ( DOID:0060162 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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