ORPHA:99047
Double outlet right ventricle with doubly committed ventricular septal defect
inactive · moved to ORPHA:423693Double outlet right ventricle with subaortic or doubly committed ventricular septal defect
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Double outlet right ventricle with subaortic or doubly committed ventricular septal defect
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Double outlet right ventricle with doubly committed ventricular septal defect | |
| fr | Ventricule droit à double issue avec communication interventriculaire sous-aortique et sous-pulmonaire | |
| de | Rechter Doppelausstromventrikel mit double-committed Ventrikelseptumdefekt | |
| es | Doble salida ventricular derecha con comunicación interventricular doblemente comprometida | |
| it | Ventricolo destro a doppia uscita con difetto del setto ventricolare doppiamente connesso | |
| nl | Rechterventrikel met dubbele uitstroom met doubly-committed ventrikelseptumdefect | |
| pt | Dupla saída do ventrículo direito com defeito do septo ventricular duplamente implicado | |
| pl | Dwuodpływowa prawa komora z ubytkiem przegrody międzykomorowej związanym z obydwoma naczyniami | |
| cs | Dvojvýtoková pravá komora s dvojitě umístěným defektem komorového septa | |
| uk | Подвійне відходження великих артерій від правого шлуночка з підартеріальним дефектом міжшлуночкової перетинки | |
| zh | 右心室双出口合并双室间隔缺损 | |
| tr | Çift katlı ventriküler septal defektli çift çıkışlı sağ ventrikül |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0344644 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/99047
- This record as JSON: /data/d/99047.json