|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset.