cerebellar ataxia

Summary
Definition
A hereditary ataxia that is characterized by ataxia originating in the cerebellum.
Super Class
cerebellar disease hereditary ataxia
External Links
Disease Ontology
DOID:0050753
Mondo Disease Ontology
MeSH
MGI genotype (from TogoID)
Related Genes
Displaying entries 31 - 37 of 37 in total
Gene ID Gene Symbol Description Source
22901 ARSG arylsulfatase G
55331 ACER3 alkaline ceramidase 3
57704 GBA2 glucosylceramidase beta 2
60481 ELOVL5 ELOVL fatty acid elongase 5
79644 SRD5A3 steroid 5 alpha-reductase 3
79944 L2HGDH L-2-hydroxyglutarate dehydrogenase
375775 PNPLA7 patatin like phospholipase domain containing 7
Displaying 1 entry
Gene ID Gene Symbol Description Source
35156 L2HGDH L-2-hydroxyglutarate dehydrogenase

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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