About   Help   FAQ
Disease Ontology Browser
dentatorubral-pallidoluysian atrophy (DOID:0060162)
Alliance: disease page
Synonyms: DRPLA; Haw River Syndrome; Naito-Oyanagi disease
Alt IDs: OMIM:125370, MESH:D020191, NCI:C122653, NCI:C7636, UMLS_CUI:C0751776, UMLS_CUI:C0751777, UMLS_CUI:C0751778, UMLS_CUI:C0751779, UMLS_CUI:C0751780, UMLS_CUI:C0751781, UMLS_CUI:C0751782
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.

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.14
The Jackson Laboratory