GB90.48ICD-11 MMS 2026-01
Disorders of calcium or phosphate excretion
Description
Conditions in which renal excretion of calcium and / or phosphate is deranged.
Index terms
- Disorders of calcium or phosphate excretion
- Phosphate losing hypophosphataemia
- hereditary hypophosphatemia
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- Phosphate losing hypophosphataemia associated with familial or genetic disorders elsewhere classified
- Familial hypophosphataemia
- Familial hypophosphatemic bone disease
- Familial hypophosphatemic osteomalacia
- Vitamin-D-resistant osteomalacia
- Acquired hyperphosphaturia or hypophosphataemia
- Hypophosphatemia, not otherwise specified
- Hyperphosphaturia
- Renal hypophosphatemia
- Hyperphosphatemia
Exclusions from above levels
Foundation children elsewhere
Sibling codes
GB90.40– Hypotonia-cystinuria type 1GB90.41– Pseudohypoaldosteronism type 1GB90.42– Fanconi syndromeGB90.43– Bartter syndromeGB90.44– Renal tubular acidosisGB90.45– Renal glycosuriaGB90.46– Tubular disorders of sodium or potassium transportGB90.47– AminoaciduriaGB90.49– Renal hypocalciuriaGB90.4A– Nephrogenic diabetes insipidusGB90.4Y– Other specified renal tubular function disordersGB90.4Z– Renal tubular function disorders, unspecified
Foundation entity
Disorders of calcium or phosphate excretion – http://id.who.int/icd/entity/1140842756
Part of: GB90.4: Renal tubular function disorders › GB90: Certain specified disorders of kidney or ureter › 16: Diseases of the genitourinary system