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Summary Literature (0)
DOID:1440 - Machado-Joseph disease

Disease Ontology Definition:An autosomal dominant cerebellar 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.

Synonyms: Azorean disease, MJD, SCA3, spinocerebellar ataxia 3, spinocerebellar ataxia type 3,

Xenbase Genes : atxn3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007182 - Machado-Joseph disease


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant cerebellar ataxia (is_a)