ORPHA:68411
Rare bone tumor
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare bone tumor | |
| fr | Tumeur osseuse rare | |
| de | Knochentumor, seltener | |
| es | Tumor óseo raro | |
| it | Tumore osseo raro | |
| nl | Zeldzame bottumor | |
| pt | Rare bone tumor | |
| pl | Rzadkie guzy kości | |
| cs | Vzácné kostní nádory | |
| uk | Рідкісна пухлина кісток | |
| zh | 罕见骨肿瘤 | |
| tr | Nadir kemik tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19060 | E | validated | |
| UMLS | C5681337 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:93419Rare bone disease
rare bone diseases - ORPHA:98057Rare tumor
rare neoplastic diseases
Children (14):
- ORPHA:55881Adamantinoma
- ORPHA:480553Aneurysmal bone cyst
- ORPHA:223727Bone sarcoma
- ORPHA:696078Central giant cell granuloma
- ORPHA:404507Chondromyxoid fibroma
- ORPHA:178Chordoma
- ORPHA:85182Diaphyseal medullary stenosis-bone malignancy syndrome
- ORPHA:435329Familial ossifying fibroma
- ORPHA:163634Maffucci syndrome
- ORPHA:321Multiple osteochondromas
- ORPHA:2760OSLAM syndrome
- ORPHA:296Ollier disease
- ORPHA:58040Osteoblastoma
- ORPHA:83468Solitary bone cyst
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/68411
- This record as JSON: /data/d/68411.json