Metal Metabolism, Inborn Errors D008664

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors

Description

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

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Subtype Terms (7)

Hemochromatosis
11 drugs (7 approved, 4 experimental)

Hepatolenticular Degeneration
21 drugs (11 approved, 10 experimental)

Hypophosphatasia
2 drugs (1 approved, 1 experimental)

Hypophosphatemia, Familial
4 drugs (3 approved, 1 experimental)

Menkes Kinky Hair Syndrome
3 drugs (1 approved, 2 experimental)

Paralyses, Familial Periodic
 

Pseudohypoparathyroidism
3 approved drugs


Organization Involved with Phase 2 Indications (2)

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UMLS Data


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