WormBase Tree Display for DO_term: DOID:0060162
expand all nodes | collapse all nodes | view schema
| DOID:0060162 | Name | dentatorubral-pallidoluysian atrophy | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| 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. | ||||
| Synonym | Exact | DRPLA | |||
| Haw River Syndrome | |||||
| Naito-Oyanagi disease | |||||
| Parent | Is_a | DOID:1441 | |||
| DB_info | Database | OMIM | disease | 125370 | |
| Attribute_of | Gene_by_orthology | WBGene00001194 |
