spinocerebellar ataxia type 2

Summary
Definition
An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene.
Super Class
autosomal dominant cerebellar ataxia
External Links
Disease Ontology
DOID:0050955
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
847 CAT catalase
6391 SDHC succinate dehydrogenase complex subunit C
27306 HPGDS hematopoietic prostaglandin D synthase
60481 ELOVL5 ELOVL fatty acid elongase 5
151056 PLB1 phospholipase B1

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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