ORPHA:352540
Oncogenic osteomalacia
Also called Oncogenic hypophosphatemic osteomalacia, TIO, Tumor-induced osteomalacia
- Body system
- Bone diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- All ages
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:352540 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Renal phosphate wasting
- Muscle weakness
- Hypophosphatemia
- Pathologic fracture
- Hyperphosphaturia
- Elevated circulating alkaline phosphatase concentration