osteopetrosis
MeSH: D010022ORPHA: 2781
Overview
an extremely rare inherited disorder whereby the bones harden, becoming denser, sometimes causing bones to dissolve and break, caused by malfunctioning osteoclasts’ inability to resorb bone
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
D010022Orphanet Code
ORPHA:2781osteopetrosis
| MeSH | D010022 |
| Orphanet | ORPHA:2781 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO