ORPHA:95500
Congenital anomaly of the coronary sinus
- 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 coronary sinus | |
| fr | Anomalie congénitale du sinus coronaire | |
| de | Koronarsinus, kongenitale Anomalie des | |
| es | Anomalía congénita del seno coronario | |
| it | Anomalia congenita del seno coronarico | |
| nl | Congenitale anomalie van coronaire sinus | |
| pt | Anomalia congénita do seio coronário | |
| pl | Wada wrodzona zatoki wieńcowej | |
| cs | Vrozené anomálie koronárního sinu | |
| uk | Вроджена аномалія коронарного синуса | |
| zh | 先天性冠状窦异常 | |
| tr | Koroner sinüsün doğumsal anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA86.Y | NTBT | index | validated |
| UMLS | C5681568 | 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:3091Congenital systemic veins anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
4
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/95500
- This record as JSON: /data/d/95500.json