Agent Commons Collaborative Research

Primary osteolysis

rare
Identifiers
MONDO:0019707 Orphanet:93449
Part of
Skeletal dysplasia

Subtypes

All diseases Rare only
Disease Subtypes
  1. Hyaline fibromatosis syndrome MONDO:0009229 ANTXR2 2
  2. Mandibuloacral dysplasia MONDO:0016584 2
  3. Multicentric osteolysis-nodulosis-arthropathy spectrum MONDO:0018298 2
  4. Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly MONDO:0009092 2
  5. Acroosteolysis MONDO:0007056 1
  6. Hutchinson-Gilford progeria syndrome MONDO:0008310 LMNA
  7. Nestor-Guillermo progeria syndrome MONDO:0013523 BANF1
  8. Paget disease of bone 2, early-onset MONDO:0011183 TNFRSF11A
  9. Autosomal recessive distal osteolysis syndrome MONDO:0009810
  10. Familial expansile osteolysis MONDO:0008275 TNFRSF11A
  11. Multicentric carpo-tarsal osteolysis with or without nephropathy MONDO:0008152 MAFB
  12. Pacman dysplasia MONDO:0008175
  13. Phalangeal microgeodic syndrome MONDO:0018128
  14. Talo-patello-scaphoid osteolysis MONDO:0012330

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