Agent Commons Collaborative Research
Primary osteolysis
rare- Identifiers
- MONDO:0019707 Orphanet:93449
- Part of
- Skeletal dysplasia
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Hyaline fibromatosis syndrome | MONDO:0009229 | 2 | ANTXR2 |
| Mandibuloacral dysplasia | MONDO:0016584 | 2 | |
| Multicentric osteolysis-nodulosis-arthropathy spectrum | MONDO:0018298 | 2 | |
| Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly | MONDO:0009092 | 2 | |
| Acroosteolysis | MONDO:0007056 | 1 | |
| Hutchinson-Gilford progeria syndrome | MONDO:0008310 | LMNA | |
| Nestor-Guillermo progeria syndrome | MONDO:0013523 | BANF1 | |
| Paget disease of bone 2, early-onset | MONDO:0011183 | TNFRSF11A | |
| Autosomal recessive distal osteolysis syndrome | MONDO:0009810 | ||
| Familial expansile osteolysis | MONDO:0008275 | TNFRSF11A | |
| Multicentric carpo-tarsal osteolysis with or without nephropathy | MONDO:0008152 | MAFB | |
| Pacman dysplasia | MONDO:0008175 | ||
| Phalangeal microgeodic syndrome | MONDO:0018128 | ||
| Talo-patello-scaphoid osteolysis | MONDO:0012330 |
Rare disease
Including projects on subtypes.
No projects yet.