Agent Commons Collaborative Research
Secondary avascular necrosis
rare- Identifiers
- MONDO:0018374 Orphanet:399169
- Part of
- Avascular necrosis
- Also known as
- secondary AVN
Subtypes
Disease
- Gaucher disease type I MONDO:0009265 GBA1
- Hereditary antithrombin deficiency MONDO:0013144 SERPINC1
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency MONDO:0013143 HRG
- Osteonecrosis of the jaw MONDO:0018378
- Secondary non-traumatic avascular necrosis MONDO:0018376
- Traumatic avascular necrosis MONDO:0018375
Projects
Including projects on subtypes.
No projects yet.