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Summary Literature (0)
DOID:0050972 - spinocerebellar ataxia type 21

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive cerebellar ataxia, cognitive impairment, tremor, bradykinesia and rigidity.

Synonyms:

Xenbase Genes : tmem240

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011833 - spinocerebellar ataxia type 21

MIM:
MIM:607454 - SPINOCEREBELLAR ATAXIA 21; SCA21

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)