5C64.1ICD-11 MMS 2026-01
Disorders of iron metabolism
Description
This refers to any disorders of the set of chemical reactions maintaining human homeostasis of iron. The control of this necessary but potentially toxic substance is an important part of many aspects of human health and disease.
Excludes
Exclusions from above levels
5B57– Vitamin D deficiency5B5K– dietary mineral deficiency- http://id.who.int/icd/entity/962023213 – Disorders of the parathyroids or parathyroid hormone system
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3A10.Z– Hereditary haemolytic anaemia due to enzyme deficiency5A71.01– Congenital adrenal hyperplasia5A81.1– 5-alpha-reductase deficiencyLD28.01– Marfan syndromeLD28.1– Ehlers-Danlos syndromeLD2A.4– androgen resistance syndrome18– Pregnancy, childbirth or the puerperium- http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn
Child codes
Sibling codes
5C64.0– Disorders of copper metabolism5C64.2– Disorders of zinc metabolism5C64.3– Disorders of phosphorus metabolism or phosphatases5C64.4– Disorders of magnesium metabolism5C64.5– Disorders of calcium metabolism5C64.6– Disorders of sodium metabolism5C64.7– Disorders of chloride metabolism5C64.Y– Disorders of other specified mineral absorption or transport5C64.Z– Disorders of mineral absorption or transport, unspecified
Foundation entity
Disorders of iron metabolism – http://id.who.int/icd/entity/396058882
Part of: 5C64: Disorders of mineral absorption or transport › 05: Endocrine, nutritional or metabolic diseases