| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A spinocerebellar ataxia that is characterized by slow degeneration of the hindbrain and has_material_basis_in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene. (Human Disease Ontology, DOID_1440) |
| External Link | http://www.omim.org/entry/109150 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the machado-joseph disease phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ATXN3 | ataxin 3 |
