Congenital patent ductus arteriosus aneurysm
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare, congenital, arterial duct anomaly characterized by a saccular dilatation of the ductus arteriosus. It is often asymptomatic or presents shortly after birth with respiratory distress, stridor, cyanosis and/or weak cry. Complications, such as rupture, thromboembolism, infection, airway erosion and/or compression of the adjacent thoracic structures, can develop. Spontaneous resolution has been reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital patent ductus arteriosus aneurysm | |
| fr | Anévrisme du canal artériel | |
| de | Aneurysma des persistierenden Ductus arteriosus, kongenitales | |
| es | Aneurisma congénito del ductus arterioso persistente | |
| it | Aneurisma congenito del dotto arterioso pervio | |
| nl | Congenitaal aneurysma van persisterende ductus arteriosus | |
| pt | Aneurisma do canal arterial patente congénito | |
| pl | Wrodzony tętniak przetrwałego przewodu tętniczego | |
| cs | Vrozené aneuryzma ductus arteriosus pantens | |
| uk | Вроджена аневризма відкритої артеріальної протоки | |
| zh | 先天性动脉导管未闭动脉瘤 | |
| tr | Doğumsal açık duktus arteriyozus anevrizması |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q25.8 | NTBT | attributed | validated |
| ICD-11 | LA8B.Y | NTBT | index | validated |
| MONDO | 0020412 | E | validated | |
| UMLS | C4706391 | 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:95485Arterial duct anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
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/99072
- This record as JSON: /data/d/99072.json