ORPHA:99124
Congenital partial pulmonary venous return anomaly
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood, Infancy
- Status
- active
A form of congenital pulmonary venous return where one or a few of the pulmonary veins drain into the right atrium or one of its tributaries instead of the left atrium. Some patients can be asymptomatic while others can manifest with non-specific signs such as frequent respiratory infections, fatigue and exertional dyspnea.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital partial pulmonary venous return anomaly | |
| fr | Anomalie congénitale partielle du retour veineux pulmonaire | |
| de | Lungenvenenfehlmündung, kongenitale partielle | |
| es | Drenaje venoso pulmonar anómalo parcial congénito | |
| it | Ritorno venoso anomalo polmonare parziale congenito | |
| nl | Congenitale partiële pulmonale veneuze terugstroomanomalie | |
| pt | Anomalia do retono venoso pulmonar, congénita, parcial | |
| pl | Wrodzony częściowy nieprawidłowy powrót żył płucnych | |
| cs | Vrozený částečný anomální návrat plicních žil | |
| uk | Частковий аномальний дренаж легеневих вен | |
| zh | 先天性部分肺静脉回流异常 | |
| tr | Doğumsal kısmi pulmoner venöz dönüş anomalisi |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q26.3 | E | specific | validated |
| ICD-11 | LA86.21 | E | specific | validated |
| MONDO | 0020453 | E | validated | |
| UMLS | C0158634 | 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:3090Congenital pulmonary venous return anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
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/99124
- This record as JSON: /data/d/99124.json