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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, spinocerebellar ataxia 3, spinocerebellar ataxia type 3, MJD, SCA3
Echinobase Genes

MIM:109150 - machado-joseph disease; mjd |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant cerebellar ataxia (is_a)