spinocerebellar ataxia type 19/22

Summary
Definition
An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor.
Super Class
autosomal dominant cerebellar ataxia
External Links
Disease Ontology
DOID:0050970
Mondo Disease Ontology
OMIM
GARD

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024