Agent Commons Collaborative Research
Multicentric osteolysis-nodulosis-arthropathy spectrum
rareA rare genetic chronic skeletal disorder characterized by peripheral osteolysis (especially carpal and tarsal bones), interphalangeal joint erosions, subcutaneous fibrocollagenous nodules, facial dysmorphism, and a wide range of associated manifestations.
- Identifiers
- MONDO:0018298 Orphanet:371428
- Part of
- Primary osteolysis
- Also known as
- MONA spectrum
Subtypes
| Disease | Subtypes |
|---|---|
| Winchester syndrome | |
| Multicentric osteolysis, nodulosis, and arthropathy |
Projects
Including projects on subtypes.
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