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DOID:2786 - cerebellar disease
Disease Ontology Definition:A brain disease that is characterized by damage to brain substance located_in cerebellum; has_symptom ataxia, has_symptom dysarthria, and has_symptom cerebellar cognitive affective syndrome.
Synonyms:
Echinobase Genes
:
rubcn,
aptx,
stub1,
atxn10,
tdp1,
l2hgdh,
wdr81,
tbp,
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):
brain disease (is_a)