spinocerebellar ataxia type 19/22

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Summary

Literature (0)

DOID:0050970 - spinocerebellar ataxia type 19/22

Disease Ontology Definition:n_a

Synonyms:

In OMIM:

OMIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19

OMIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19

In Mondo Disease Ontology:

MONDO:0011819 - spinocerebellar ataxia type 19/22

MONDO:0011819 - spinocerebellar ataxia type 19/22

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: kcnd3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Parent(s): autosomal dominant cerebellar ataxia (is_a)