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Summary Literature (0)
DOID:0050970 - spinocerebellar ataxia type 19/22

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor.

Synonyms:

Xenbase Genes : kcnd3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011819 - spinocerebellar ataxia type 19/22

MIM:
MIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19

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)