Spinocerebellar Ataxia Type 38

About the Disease
Spinocerebellar Ataxia 38, also known as spinocerebellar ataxia type 38, is related to hereditary ataxia and autosomal dominant cerebellar ataxia, and has symptoms including cerebellar ataxia and gait ataxia. An important gene associated with Spinocerebellar Ataxia 38 is ELOVL5 (ELOVL Fatty Acid Elongase 5), and among its related pathways/superpathways are Metabolism and Fatty acid metabolism. The drug Omega 3 Fatty Acid has been mentioned in the context of this disorder. Affiliated tissues include spinal cord, cerebellum and brain, and related phenotypes are nystagmus and dysarthria

Common Targets
ELOVL5

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