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DOID:0050951 - hereditary ataxia
Disease Ontology Definition:A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
Synonyms:
Echinobase Genes
:
rubcn,
mars2,
aptx,
stub1,
twnk,
atxn10,
wdr81,
tbp,
mtpap,
itpr1,
ca8,
ano10,
afg3l2,
eef2
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
neurodegenerative disease (is_a)