autosomal dominant hypophosphatemic rickets
ICD-10: E83.3MeSH: C562791ORPHA: 89937
Overview
rickets characterized by low levels of serum phosphate and elevated levels of ALP and phosphaturia and that has material basis in autosomal dominant inheritance
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with autosomal dominant hypophosphatemic rickets, sourced from HPO and Orphanet clinical annotations.
HypophosphatemiaHyperphosphaturiaMuscle weaknessGrowth delayIron deficiency anemiaBone painRicketsOsteomalaciaBowing of the legsElevated circulating alkaline phosphatase concentrationFatigueTooth abscessDecreased circulating vitamin D concentrationBone fractureHypocalcemia
Classification & Codes
ICD-10 Code
E83.3MeSH Code
C562791Orphanet Code
ORPHA:89937autosomal dominant hypophosphatemic rickets
| ICD-10 | E83.3 |
| MeSH | C562791 |
| Orphanet | ORPHA:89937 |
| Treatments | 0 drug(s) |
| Symptoms on record | 15 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO