Category:Inborn errors of metal metabolism

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Inborn error of metal metabolism (E83, 275)

Transition metal

high:	Primary iron overload disorder: Hemochromatosis/HFE1 Juvenile/HFE2 HFE3 African iron overload/HFE4 Aceruloplasminemia Atransferrinemia Hemosiderosis
deficiency:	Iron deficiency

high:	Copper toxicity Wilson's disease
deficiency:	Copper deficiency Menkes disease/Occipital horn syndrome

high:	Zinc toxicity
deficiency:	Acrodermatitis enteropathica

Na⁺ and K⁺

see Template:Water-electrolyte imbalance and acid-base imbalance

high:	Hyperphosphatemia
deficiency:	Hypophosphatemia alkaline phosphatase Hypophosphatasia

high:	Hypermagnesemia
deficiency:	Hypomagnesemia

high:	Hypercalcaemia Milk-alkali syndrome (Burnett's) Calcinosis (Calciphylaxis, Calcinosis cutis) Calcification (Metastatic calcification, Dystrophic calcification) Familial hypocalciuric hypercalcemia
deficiency:	Hypocalcaemia Osteomalacia Pseudohypoparathyroidism (Albright's hereditary osteodystrophy) Pseudopseudohypoparathyroidism

v t e Index of nutrition
Description	Vitamins metabolism Cofactors Metal metabolism Fats metabolism intermediates lipoproteins Sugars Glycolysis enzymes Glycogenesis and glycogenolysis intermediates Fructose and galactose intermediates
Disease	Vitamins Carbohydrate Lipid storage Metals Other Symptoms and signs Tests
Treatment	Drugs obesity lipid-modifying Vitamins Mineral supplements

Pages in category "Inborn errors of metal metabolism"

The following 9 pages are in this category, out of 9 total.

A

D

Disorders of calcium metabolism

H

Hypercalciuria

I

Inborn errors of metal metabolism

M

Menkes disease

O

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