ORPHA:235832
Congenital vascular bone syndrome
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital vascular bone syndrome | |
| fr | Syndrome vasculaire osseux congénital | |
| de | Gefäßknochensyndrom, kongenitales | |
| es | Síndrome óseo vascular congénito | |
| it | Sindrome vascolare ossea congenita | |
| nl | Congenitaal vasculair botsyndroom | |
| pt | Síndrome de osso vascular congénito | |
| pl | Wrodzony zespół waskularyzacji kości | |
| cs | Vrozený vaskulární syndrom kostí | |
| uk | Вроджений судинно-кістковий синдром | |
| zh | 先天性血管骨综合征 | |
| tr | Doğumsal vasküler kemik sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD26.6 | E | specific | validated |
| MONDO | 16524 | E | validated | |
| UMLS | C5680924 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:93419Rare bone disease
rare bone diseases - ORPHA:183524Rare genetic bone disease
rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:235835OBSOLETE: Congenital vascular bone syndrome with limb overgrowth referred to · inactive
- ORPHA:235838OBSOLETE: Congenital vascular bone syndrome with limb shortening referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/235832
- This record as JSON: /data/d/235832.json