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Terminology chevron_right Concepts chevron_right 154751003

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The component that hold information about this concept.
Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease])
Iron disorder
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease])

SCTID: 154751003, Primitive, Inactive


154751003|Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease])|
  • en Copper disorder
  • en Haemochromatosis
  • en Hemochromatosis
  • en Iron, copper, magnesium disord
  • en Iron, copper, magnesium metabolism disorder
  • en Iron disorder
  • en Magnesium disorder
  • en Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease]) (disorder)
  • en Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease])
  • en Iron &/or copper &/or magnesium disorder (& [hemochromatosis] or [wilson's disease])
  • en Wilson's disease

154751003 |Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [wilson's disease])|

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