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Disease Metal Metabolism, Inborn Errors

Name Metal Metabolism, Inborn Errors
Synonym Metal Metabolism, Inborn Error
Definition Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID D008664
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes

Top ↑ Descendants

Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes
  Congenital atransferrinemia Has associated chemicals Has associated genes
  Copper Toxicosis, Idiopathic Has associated chemicals Has associated genes
View node Hemochromatosis Has associated chemicals Has associated genes
View node Hepatolenticular Degeneration Has associated chemicals Has associated genes
  Hyperzincemia and Hypercalprotectinemia
  Hyperzincemia with Functional Zinc Depletion
View node Hypophosphatasia Has associated chemicals Has associated genes
View node Hypophosphatemia, Familial Has associated chemicals Has associated genes
View node Menkes Kinky Hair Syndrome Has associated chemicals Has associated genes
  Molybdenum cofactor deficiency Has associated chemicals Has associated genes
  Molybdenum Cofactor Deficiency, Complementation Group A
  Molybdenum Cofactor Deficiency, Complementation Group B Has associated chemicals Has associated genes
  Molybdenum Cofactor Deficiency, Complementation Group C Has associated chemicals Has associated genes
View node Paralyses, Familial Periodic Has associated chemicals Has associated genes
View node Pseudohypoparathyroidism Has associated chemicals Has associated genes
  ZINC, ELEVATED PLASMA