A benign, intermediate, or malignant neoplasm involving the bone or articular cartilage.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Bone cancer | MONDO:0002129 | 232 | |
| Skull neoplasm | MONDO:0024653 | 128 | |
| Bone benign neoplasm | MONDO:0000631 | 31 | |
| Notochordal tumor | MONDO:0002597 | 8 | |
| Vascular bone neoplasm | MONDO:0024499 | 4 | |
| Hereditary multiple osteochondromas | MONDO:0005508 | 3 | |
| Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone | MONDO:0021123 | 2 | |
| Neoplasm of femur | MONDO:0021579 | 1 | |
| OSLAM syndrome | MONDO:0008139 | ||
| Ollier disease | MONDO:0008145 | ||
| Aneurysmal bone cyst | MONDO:0018815 | ||
| Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome | MONDO:0033683 | MYSM1 | |
| Diaphyseal medullary stenosis-bone malignancy syndrome | MONDO:0007205 | MTAP | |
| Hyperparathyroidism 1 | MONDO:0007767 | CDC73 | |
| Hyperparathyroidism 2 with jaw tumors | MONDO:0007768 | ||
| Hyperparathyroidism 3 | MONDO:0012406 | ||
| Hyperparathyroidism 4 | MONDO:0024570 | GCM2 | |
| Juvenile hyaline fibromatosis | MONDO:0016071 | ||
| Neonatal severe primary hyperparathyroidism | MONDO:0009397 | CASR | |
| Solitary bone cyst | MONDO:0019372 |
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