5C63.22ICD-11 MMS 2026-01
Hypophosphataemic rickets
Description
Hypophosphatemic rickets is a group of genetic diseases characterised by hypophosphatemia, rickets, and normal serum levels of calcium.
Index terms
- Hypophosphataemic rickets
- HPDR - [hypophosphatemic vitamin d-resistant rickets]
- VDRR - [vitamin-D-resistant rickets]
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- Vitamin-D-resistant rickets
- Autosomal dominant hypophosphataemic rickets
- ADHR - [autosomal dominant hypophosphataemic rickets]
- Autosomal dominant hypophosphataemia
- Autosomal recessive hypophosphataemic rickets
- ARHR - [autosomal recessive hypophosphataemic rickets]
- Autosomal recessive hypophosphataemia
- Hypophosphataemic rickets with hypercalciuria
- X-linked hypophosphataemia
- X-linked hypophosphatemic rickets
- familial x-linked hypophosphatemic vitamin d refractory rickets
- x-linked vitamin d-resistant rickets
- X-linked hypophosphatemic osteomalacia
- Familial hypophosphataemic rickets
- familial vitamin d-resistant rickets
Exclusions from above levels
Sibling codes
Foundation entity
Hypophosphataemic rickets – http://id.who.int/icd/entity/1010293846
Part of: 5C63.2: Disorders of vitamin D metabolism or transport › 5C63: Disorders of vitamin or non-protein cofactor absorption or transport › 05: Endocrine, nutritional or metabolic diseases