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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:
Xenbase Genes
:
fgf14,
slc9a1,
tbp,
ifrd1,
tubb2b,
ttbk2,
atm,
prkcg,
atxn2,
itpr1,
vps13d,
afg3l2,
ppp2r2b,
tdp1,
elovl5,
| MONDO:0000557 - obsolete hereditary ataxia |
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)