3-methylglutaconic Aciduria Type I

About the Disease
3-Methylglutaconic Aciduria, Type I, also known as 3-methylglutaconyl-coa hydratase deficiency, is related to 3-methylglutaconic aciduria, type iv and 3-methylglutaconic aciduria, and has symptoms including athetosis and cerebellar ataxia. An important gene associated with 3-Methylglutaconic Aciduria, Type I is AUH (AU RNA Binding Methylglutaconyl-CoA Hydratase). Affiliated tissues include brain, skeletal muscle and placenta, and related phenotypes are failure to thrive and 3-methylglutaconic aciduria

Common Targets
AUH

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