ORPHA:211240
Genetic vascular anomaly
- 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 | Genetic vascular anomaly | |
| fr | Anomalie vasculaire génétique | |
| de | Vaskuläre Anomalie, genetisch bedingte | |
| es | Anomalía genética vascular | |
| it | Anomalia vascolare genetica | |
| nl | Genetische vasculaire anomalie | |
| pt | Anomalia vascular genética | |
| pl | Anomalia naczyniowa uwarunkowana genetycznie | |
| cs | Geneticky podmíněné vaskulární anomálie | |
| uk | Генетично обумовлена судинна аномалія | |
| zh | 遗传性血管异常 | |
| tr | Genetik vasküler anomali |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16229 | E | validated | |
| UMLS | C5680854 | 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:183530Rare genetic developmental defect during embryogenesis
rare genetic diseases
Children (11):
- ORPHA:46724Brain arteriovenous malformation, nidus type
- ORPHA:137667Capillary malformation-arteriovenous malformation
- ORPHA:717619Capillary-lymphatic-venous malformation
- ORPHA:717611Capillary-venous malformation
- ORPHA:466729Familial patent arterial duct
- ORPHA:459537Genetic complex vascular malformation with associated anomalies
- ORPHA:77240Primary lymphedema
- ORPHA:459526Rare genetic capillary malformation
- ORPHA:459543Rare genetic vascular tumor
- ORPHA:459548Rare genetic venous malformation
- ORPHA:1053Vein of Galen malformation
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/211240
- This record as JSON: /data/d/211240.json