ORPHA:363189
Congenital anomaly of the great veins
- 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 | Congenital anomaly of the great veins | |
| fr | Anomalie congénitale des veines de gros calibre | |
| de | Großen Venen, kongenitale Anomalie der | |
| es | Anomalía congénita de los grandes vasos | |
| it | Anomalia congenita delle grandi vene | |
| nl | Congenitale anomalie van grote aders | |
| pt | Anomalia congénita das grandes veias | |
| pl | Wady wrodzone dużych żył | |
| cs | Vrozené anomálie velkých žil | |
| uk | Вроджена аномалія великих вен | |
| zh | 先天性大静脉畸形 | |
| tr | Büyük damarların doğumsal anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18185 | E | validated | |
| UMLS | C0158632 | E | validated | |
| MedDRA | 10061080 | 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:88991Rare congenital heart disease
rare developmental anomalies during embryogenesis; rare cardiac malformations - ORPHA:458844Rare vascular malformation of major vessels
rare developmental anomalies during embryogenesis; rare circulatory system diseases
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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/363189
- This record as JSON: /data/d/363189.json