ORPHA:211277
Syndromic combined vascular malformation
Synonyms: Complex vascular malformation with associated anomalie
- 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 | Syndromic combined vascular malformation | Complex vascular malformation with associated anomalie |
| fr | Malformation vasculaire combinée syndromique | Malformation vasculaire complexe avec anomalies associées |
| de | Syndromale kombinierte vaskuläre Fehlbildung | Komplexe vaskuläre Malformation mit begleitender Anomalie · Hämangiolymphangiom · Syndromale kombinierte vaskuläre Malformation |
| es | Malformación vascular combinada sindrómica | Malformación vascular completa con anomalías asociadas |
| it | Malformazione vascolare combinata sindromica | Malformazione vascolare complessa con anomalie associate |
| nl | Syndromale gecombineerde vasculaire malformatie | Syndromale gecombineerde vaatmalformatie · Complexe vasculaire malformatie met geassocieerde anomalie |
| pt | Malformação vascular complexa/combinada | |
| pl | Złożona - mieszna malformacja naczyniowa | = en |
| cs | Komplexní vaskulární malformace s přidruženými anomáliemi | Hemangiolymfangiom |
| uk | Складна судинна вада розвитку з супутніми аномаліями | Гемангіолімфангіома |
| zh | 复杂血管畸形伴相关异常 | 血管淋巴管瘤 |
| tr | İlişkili anomaliler ile seyreden kompleks vasküler malformasyon | Hemanjiyolenfanjiyom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16235 | E | validated | |
| UMLS | C5679799 | 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 (1):
- ORPHA:458837Rare combined vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
Children (4):
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/211277
- This record as JSON: /data/d/211277.json