Accessory tricuspid valve tissue
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare, congenital, atrioventricular valve malformation characterized by fixed or mobile accessory tissue on the tricuspid valve, usually associated with other complex congenital heart anomalies (atrial septal defect, ventricular septal defect, transposition of great arteries, tetralogy Fallot). It may present clinically with systolic murmur, dyspnea, cyanosis, depending also on accompanying congenital heart anomaly.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Accessory tricuspid valve tissue | |
| fr | Tissu accessoire tricuspide | |
| de | Trikuspidalklappe mit akzessorischem Gewebe | |
| es | Tejido accesorio de la válvula tricúspide | |
| it | Tessuto accessorio della valvola tricuspide | |
| nl | Bijkomstig tricuspidalisklepweefsel | |
| pt | Válvula tricúspide, tecido acessório | |
| pl | Dodatkowa tkanka zastawki tródzielnej | |
| cs | Přídatná tkáň trikuspidální chlopně | |
| uk | Додаткові тканини трикуспідального клапана | |
| zh | 三尖瓣副瓣 | |
| tr | Aksesuar triküspit kapak dokusu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q22.8 | NTBT | attributed | validated |
| ICD-11 | LA87.0Y | NTBT | attributed | validated |
| MONDO | 0019815 | E | validated | |
| UMLS | C5566613 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98721Congenital tricuspid malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95462
- This record as JSON: /data/d/95462.json