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)
Similar Terms
Downloads & Tools
Genes
1 genes associated with the disease machado-joseph disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
