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