ORPHA:458837
Rare combined vascular malformation
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare combined vascular malformation | |
| fr | Malformation vasculaire combinée rare | |
| de | Seltene kombinierte vaskuläre Fehlbildung | Seltene kombinierte vaskuläre Malformation |
| es | Malformación vascular combinada rara | |
| it | Malformazione vascolare combinata | |
| nl | Zeldzame gecombineerde vasculaire malformatie | |
| pt | Malformação vascular combinada | |
| pl | Rzadka złożona malformacja naczyniowa | |
| cs | Vzácné kombinované cévní malformace | |
| uk | Рідкісна комбінована судинна вада розвитку | |
| zh | 罕见联合血管畸形 | |
| tr | Nadir kombine vasküler malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18721 | E | validated | |
| UMLS | C5681115 | 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 (1):
- ORPHA:723256Rare vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/458837
- This record as JSON: /data/d/458837.json