osteomesopyknosis
MeSH: C537792ORPHA: 2777
Overview
Osteomesopyknosis is a very rare benign bone disorder characterized by bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content
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 osteomesopyknosis, sourced from HPO and Orphanet clinical annotations.
Increased bone mineral densityScoliosisKyphosisAbnormal form of the vertebral bodiesSclerotic vertebral bodyAbnormality of metabolism/homeostasisAbnormal cortical bone morphology
Classification & Codes
MeSH Code
C537792Orphanet Code
ORPHA:2777osteomesopyknosis
| MeSH | C537792 |
| Orphanet | ORPHA:2777 |
| Treatments | 0 drug(s) |
| Symptoms on record | 7 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO