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ENMolybdenum Cofactor Deficiency (MOCOD)
Alias:
Combined Molybdoflavoprotein Enzyme Deficiency
Mocod
Combined Deficiency of Sulfite Oxidase, Xanthine Dehydrogenase, and Aldehyde Oxidase
Combined Deficiency of Sulfite Oxidase, Xanthine Dehydrogenase and Aldehyde Oxidase
Combined Xanthine Oxidase and Sulfite Oxidase and Aldehyde Oxidase Deficiency
Deficiency of Molybdenum Cofactor
Deficiency, Molybdenum Cofactor
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Molybdenum Cofactor Deficiency, also known as combined molybdoflavoprotein enzyme deficiency, is related to molybdenum cofactor deficiency, complementation group c and molybdenum cofactor deficiency, complementation group b. An important gene associated with Molybdenum Cofactor Deficiency is MOCS1 (Molybdenum Cofactor Synthesis 1), and among its related pathways/superpathways are Metabolism and Metabolism of water-soluble vitamins and cofactors. Affiliated tissues include brain, and related phenotype is renal/urinary system.
Related ID：
MESH：C535811
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MALACARDS
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