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Taxonomy hierarchy

Pyruvate Carboxylase Deficiency Disease

AMW:DIS:100119

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Brain Diseases, Metabolic, InbornMetabolic DisorderMitochondrial DiseasesMetabolic DisorderPyruvate Metabolism, Inborn ErrorsCongenital Disorder
Focus nodePyruvate Carboxylase Deficiency DiseaseAMW:DIS:100119

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