ORPHA:68419
Rare 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 | Rare vascular anomaly | |
| fr | Anomalie vasculaire rare | |
| de | Seltene vaskuläre Fehlbildung | |
| es | Angioma o malformación vascular | |
| it | Angioma o difetto vascolare | |
| nl | Vasculaire anomalie of angioom | |
| pt | Angioma ou malformação vascular | |
| pl | Anomalie naczyniowe lub naczyniaki | |
| cs | Vaskulární anomálie nebo angiomy | |
| uk | Рідкісна судинна аномалія | |
| zh | 血管异常或血管瘤 | |
| tr | Vasküler anomali veya anjiyom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19063 | E | validated | |
| UMLS | C5925045 | 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:98028Rare circulatory system disease
rare circulatory system diseases - ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
Codes that Orphanet moved or referred to this one:
- ORPHA:2039OBSOLETE: Congenital systemic arteriovenous fistula referred to · inactive
- ORPHA:2346OBSOLETE: Angioosteohypertrophic syndrome referred to · inactive
- ORPHA:98731OBSOLETE: Congenital arteriovenous fistula 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.
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/68419
- This record as JSON: /data/d/68419.json