Metal Metabolism, Inborn Errors

Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.

Year introduced: 1965

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Tree Number(s): C16.320.565.618, C18.452.648.618

MeSH Unique ID: D008664

Entry Terms:

• Metal Metabolism, Inborn Error

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hemochromatosis
Hepatolenticular Degeneration
Hypophosphatasia
Hypophosphatemia, Familial
Familial Hypophosphatemic Rickets
Menkes Kinky Hair Syndrome
Paralyses, Familial Periodic
Hypokalemic Periodic Paralysis
Paralysis, Hyperkalemic Periodic
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hemochromatosis
Hepatolenticular Degeneration
Hypophosphatasia
Hypophosphatemia, Familial
Familial Hypophosphatemic Rickets
Menkes Kinky Hair Syndrome
Paralyses, Familial Periodic
Hypokalemic Periodic Paralysis
Paralysis, Hyperkalemic Periodic
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism