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Inborn Errors Metal Metabolism
Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.
Also Known As:
Metal Metabolism, Inborn Errors; Metal Metabolism, Inborn Error
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Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Inborn Errors Metal Metabolism
Hemochromatosis: 4165
Hepatolenticular Degeneration: 3939
Pseudohypoparathyroidism: 756
Hypophosphatasia: 737
Menkes Kinky Hair Syndrome: 729
Familial Hypophosphatemia: 721
Molybdenum cofactor deficiency: 85
Familial Periodic Paralyses: 71
Congenital atransferrinemia: 24
Idiopathic Copper Toxicosis: 16
hyperzincemia and hypercalprotectinemia: 10
Complementation Group A Molybdenum Cofactor Deficiency: 5
Complementation Group B Molybdenum Cofactor Deficiency: 5
Complementation Group C Molybdenum Cofactor Deficiency
Hyperzincemia with Functional Zinc Depletion
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Inborn Errors Metal Metabolism
Hemochromatosis: 4165
Hepatolenticular Degeneration: 3939
Pseudohypoparathyroidism: 756
Hypophosphatasia: 737
Menkes Kinky Hair Syndrome: 729
Familial Hypophosphatemia: 721
Molybdenum cofactor deficiency: 85
Familial Periodic Paralyses: 71
Congenital atransferrinemia: 24
Idiopathic Copper Toxicosis: 16
hyperzincemia and hypercalprotectinemia: 10
Complementation Group A Molybdenum Cofactor Deficiency: 5
Complementation Group B Molybdenum Cofactor Deficiency: 5
Complementation Group C Molybdenum Cofactor Deficiency
Hyperzincemia with Functional Zinc Depletion