ORPHA:216675
Transposition of the great arteries
Synonyms: Complete transposition · TGA · TGV · Transposition of the great vessels
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Multigenic/multifactorial, Not applicable
- Age of onset
- Infancy, Neonatal
- 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 | Transposition of the great arteries | Complete transposition · TGA · TGV · Transposition of the great vessels |
| fr | Transposition des gros vaisseaux | TGV · Transposition complète · Transposition des grosses artères |
| de | Transposition der großen Arterien | Komplette Transposition der großen Arterien · TGA · Transposition der großen Gefäße |
| es | Transposición de las grandes arterias | TGA · TGV · Transposición completa · Transposición de los grandes vasos |
| it | Trasposizione delle grandi arterie | TGA · TGV · Trasposizione completa · Trasposizione dei grandi vasi |
| nl | Transpositie van grote slagaders | TGA · TGV · Transpositie van grote bloedvaten · Volledige transpositie |
| pt | Transposição das grandes artérias | |
| pl | Przełożenie wielkich pni tętniczych | Całkowita transpozycja · Przełożenie wielkich naczyń · TGA · TGV |
| cs | Transpozice velkých tepen | Úplná transpozice · TGA · TGV · Transpozice velkých cév |
| uk | Транспозиція великих артерій (Транспозиція магістральних судуин) | Повна транспозиція · TGA · TGV · Переміщення великих судин |
| zh | 大动脉转位 | 大血管转位 |
| tr | Büyük arterlerin transpozisyonu | TGA · TGV · Tam transpozisyon · Büyük damarların transpozisyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA85.1 | E | specific | validated |
| MONDO | 0000153 | E | validated | |
| MONDO | 153 | E | validated | |
| MeSH | D014188 | E | validated | |
| UMLS | C0040761 | E | validated | |
| GARD | 7795 | E | validated | |
| MedDRA | 10044443 | 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:98717Transposition of the great arteries and conotruncal cardiac anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
18 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Prevalence at birth | 1-5 / 10 000 | 22.3 / 100 000 | Ukraine | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Point prevalence | 1-5 / 10 000 | — | Europe | Class only | Not yet validated | ORPHANET |
| Prevalence at birth | 1-5 / 10 000 | 31.7 / 100 000 | Europe | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 50 / 100 000 | United States | Value and class | Validated | 17051527[PMID]_Center for Diseases Control and Prevention[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 23.3 / 100 000 | Belgium | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 59.5 / 100 000 | Denmark | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 33.4 / 100 000 | France | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 47.5 / 100 000 | Germany | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 28.8 / 100 000 | Hungary | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 18.1 / 100 000 | Ireland | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 22.6 / 100 000 | Italy | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 40.9 / 100 000 | Netherlands | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 31.1 / 100 000 | Norway | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 14 / 100 000 | Poland | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-9 / 100 000 | 4.7 / 100 000 | Portugal | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 15.7 / 100 000 | Spain | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2010[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 37.7 / 100 000 | Switzerland | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
| Prevalence at birth | 1-5 / 10 000 | 33.9 / 100 000 | United Kingdom | Value and class | Validated | EUROCAT European surveillance of congenital anomalies 2011[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/216675
- This record as JSON: /data/d/216675.json