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


Disease Ontology Definition:n_a

Synonyms:

Referenced OMIM:
OMIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : kcnd3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant cerebellar ataxia (is_a)


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