5C64.3ICD-11 MMS 2026-01
Disorders of phosphorus metabolism or phosphatases
Description
Any condition caused by errors in phosphorus metabolism, or in phosphatase activity.
Index terms
- Disorders of phosphorus metabolism or phosphatases
- disorders of phosphorus metabolism
- Hypophosphatasia
Show allHide
- Rathbun syndrome
- Congenital hypophosphatasia
- Fetal hypophosphatasia
- Infantile hypophosphatasia
- infantile type hypophosphatasia
- Acid phosphatase deficiency
- Alkaline phosphatase deficiency
- Congenital hypophosphatemia
- Phosphataemia
- Phosphate diabetes
- Phosphaturia
- Renal phosphaturia
- Phosphoethanolaminuria
Inclusions
- Hypophosphatasia
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
Show allHide
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
Foundation children elsewhere
5C63.22– Hypophosphataemic rickets
Sibling codes
5C64.0– Disorders of copper metabolism5C64.1– Disorders of iron metabolism5C64.2– Disorders of zinc metabolism5C64.4– 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 phosphorus metabolism or phosphatases – http://id.who.int/icd/entity/108919913
Part of: 5C64: Disorders of mineral absorption or transport › 05: Endocrine, nutritional or metabolic diseases