Solitary bone cyst
diseaseOn this page
Also known as bone cystcyst of bonecyst of the bonesimple bone cystsolitary cystunicameral bone cyst
Summary
Solitary bone cyst (MONDO:0019372) is a disease and 13 clinical trials. A subtype of bone neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Worldwide)
- Phenotypes (HPO): 17
- Clinical trials: 13
Clinical features
Signs & symptoms
Clinical features (HPO)
17 HPO clinical features (Orphanet curated; top 17 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0012064 | Unicameral bone cyst | Very frequent (80-99%) |
| HP:0002653 | Bone pain | Frequent (30-79%) |
| HP:0002756 | Pathologic fracture | Frequent (30-79%) |
| HP:0003926 | Abnormality of the humeral diaphysis | Frequent (30-79%) |
| HP:0006431 | Proximal femoral metaphyseal abnormality | Frequent (30-79%) |
| HP:0100253 | Abnormality of the medullary cavity of the long bones | Frequent (30-79%) |
| HP:0002992 | Abnormality of tibia morphology | Occasional (5-29%) |
| HP:0012428 | Prominent calcaneus | Occasional (5-29%) |
| HP:0000707 | Abnormality of the nervous system | Very rare (<1-4%) |
| HP:0002143 | Abnormality of the spinal cord | Very rare (<1-4%) |
| HP:0002696 | Abnormal parietal bone morphology | Very rare (<1-4%) |
| HP:0002867 | Abnormality of the ilium | Very rare (<1-4%) |
| HP:0003172 | Abnormality of the pubic bone | Very rare (<1-4%) |
| HP:0003312 | Abnormal form of the vertebral bodies | Very rare (<1-4%) |
| HP:0003418 | Back pain | Very rare (<1-4%) |
| HP:0003979 | Lytic defects of the radius | Very rare (<1-4%) |
| HP:0100748 | Muscular edema | Very rare (<1-4%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | solitary bone cyst |
| Mondo ID | MONDO:0019372 |
| MeSH | D001845 |
| Orphanet | 83468 |
| ICD-10-CM | M85.4 |
| ICD-11 | 987501456 |
| NCIT | C2904 |
| SNOMED CT | 203467005 |
| UMLS | C0005937 |
| MedGen | 2696 |
| GARD | 0019039 |
| Is cancer (heuristic) | no |
Also known as: bone cyst · cyst of bone · cyst of the bone · simple bone cyst · solitary cyst · unicameral bone cyst
Disease family
This is a subtype of bone neoplasm. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › musculoskeletal system disorder › skeletal system disorder › bone disorder › bone neoplasm › solitary bone cyst
Related subtypes (19): bone benign neoplasm, bone cancer, notochordal tumor, hereditary multiple osteochondromas, diaphyseal medullary stenosis-bone malignancy syndrome, hyperparathyroidism 1, hyperparathyroidism 2 with jaw tumors, OSLAM syndrome, Ollier disease, neonatal severe primary hyperparathyroidism, hyperparathyroidism 3, juvenile hyaline fibromatosis, aneurysmal bone cyst, Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone, neoplasm of femur, vascular bone neoplasm, hyperparathyroidism 4, skull neoplasm, congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 13.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 10 |
| PHASE3 | 1 |
| PHASE2 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02193841 | PHASE3 | RECRUITING | Simple Bone Cysts in Kids |
| NCT00459641 | PHASE2 | WITHDRAWN | Safety and Tolerability of I-040302 in Children and Young Adults With Solitary Bone Cysts |
| NCT01207193 | PHASE1 | COMPLETED | Treatment Of Bone Cyst With Bone Marrow Mesenchymal Cell Transplantation |
| NCT07066228 | Not specified | RECRUITING | Bone Reconstruction With Autologous Bone Marrow Mesenchymal Stem Cells in Vitro to Repair Long Tubular Bone Defects |
| NCT02567084 | Not specified | COMPLETED | Complete Twelve Month Bone Remodeling With a Bi-phasic Injectable Bone Substitute in Benign Bone Tumors |
| NCT02575352 | Not specified | UNKNOWN | Calcium Phosphate Cement Registry (CPC Registry) |
| NCT02616757 | Not specified | WITHDRAWN | Quantitative Ultrasound for the Evaluation of Simple Bone Cyst Healing |
| NCT03076138 | Not specified | COMPLETED | Gene-activated Bone Substitute for Maxillofacial Bone Regeneration |
| NCT03724630 | Not specified | UNKNOWN | The Results of Multiple Aspirations and Injections of Unicameral Bone Cyst by Methyl Prednisolone Acetate |
| NCT04737590 | Not specified | UNKNOWN | Bioactive Glass or Allogenic Bone in Pediatric Bone Cysts |
| NCT05075148 | Not specified | UNKNOWN | Aneurysmal Bone Cyst Imaging After Interventional Radiology Treatment |
| NCT05880628 | Not specified | UNKNOWN | Evaluation of Faisability, Safety and Effectiveness and of Discogel in Patients With Aneurysmal and Simple Bone Cysts |
| NCT07379008 | Not specified | COMPLETED | Safety and Efficacy of Non-Setting Paste in Bone Defect Reconstruction |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.