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Echinobase
Summary Literature (0)
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, atxn10, tdp1, wdr81, tbp, mtpap, itpr1, ca8, ano10, afg3l2, eef2



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): neurodegenerative disease (is_a)