Summary

Alpha-Ketoglutarate Dehydrogenase Deficiency, also known as oxoglutaricaciduria,is related to lactic acidosis and wheat allergy,and has symptoms including hypertonia, incoordination and skeletal muscle atrophy. An important gene associated with Alpha-Ketoglutarate Dehydrogenase Deficiency is OGDH (Oxoglutarate Dehydrogenase), and among its related pathways are Pyruvate metabolism and Signaling by Retinoic Acid. Affiliated tissues include salivary gland and skeletal muscle, and related mousephenotype growth/size/body region

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Pathways Associated With Trait

Symptoms Associated With Trait