osteomesopyknosis
MONDO:0008155Mondo
Findings
No curated finding names osteomesopyknosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0008155), read 2026-09-29. CC BY 4.0.
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Increased bone mineral densityHPOHP:0011001
- Very frequent (80% to 99% of cases)
- Abnormal vertebral body morphologyHPOHP:0003312
- Frequent (30% to 79% of cases)
- KyphosisHPOHP:0002808
- Frequent (30% to 79% of cases)
- Sclerotic vertebral bodyHPOHP:0100861
- Frequent (30% to 79% of cases)
- ScoliosisHPOHP:0002650
- Frequent (30% to 79% of cases)
- Abnormal cortical bone morphologyHPOHP:0003103
- Occasional (5% to 29% of cases)
- Abnormality of metabolism/homeostasisHPOHP:0001939
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: osteomesopyknosis
- Also called
- axial osteosclerosis