ORPHA:98721
Congenital tricuspid malformation
- 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 tricuspid malformation | |
| fr | Malformation tricuspide congénitale | |
| de | Trikuspidalklappenfehlbildung, kongenitale | |
| es | Malformación congénita de la tricúspide | |
| it | Malformazione congenita della tricuspide | |
| nl | Congenitale tricuspidalismalformatie | |
| pt | Malformação tricúspide, congénita | |
| pl | Wady wrodzone zastawki trójdzielnej | |
| cs | Vrozené trikuspidální malformace | |
| uk | Вроджена трикуспідальна вада | |
| zh | 先天性三尖瓣畸形 | |
| tr | Doğumsal triküspit malformasyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020289 | E | validated | |
| UMLS | C5681691 | 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:98720Atrioventricular valve anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations
Children (8):
- ORPHA:95462Accessory tricuspid valve tissue
- ORPHA:95463Anomaly of the tricuspid subvalvular apparatus
- ORPHA:95459Congenital tricuspid stenosis
- ORPHA:555874Congenital tricuspid valve dysplasia
- ORPHA:1880Ebstein malformation of the tricuspid valve
- ORPHA:95461Straddling or overriding tricuspid valve
- ORPHA:1209Tricuspid atresia
- ORPHA:95457Tricuspid valve agenesis
Codes that Orphanet moved or referred to this one:
- ORPHA:95458OBSOLETE: Tricuspid valve prolapse 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.
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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/98721
- This record as JSON: /data/d/98721.json