ORPHA:474347
Rare congenital anomaly of ventricular septum
Synonyms: Congenital anomaly of interventricular communication · Congenital ventricular septal anomaly
- Type
- Clinical group
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare congenital anomaly of ventricular septum | Congenital anomaly of interventricular communication · Congenital ventricular septal anomaly |
| fr | Anomalie congénitale du septum interventriculaire rare | |
| de | Seltene kongenitale Anomalie des Ventrikelseptums | Kongenitale Anomalie der interventrikulären Kommunikation · Ventrikelseptum-Anomalie, kongenitale |
| es | Anomalía congénita rara del septo ventricular | Anomalía congénita de la comunicación interventricular · Anomalía septal ventricular congénita |
| it | Anomalia congenita del setto ventricolare | |
| nl | Zeldzame congenitale anomalie van ventrikelseptum | Congenitaal ventrikelseptumdefect · Congenitale anomalie van interventriculaire communicatie |
| pt | Anomalia congénita do septo ventricular | |
| pl | Wrodzona wada przegrody międzykomorowej | = en |
| cs | Vzácný vrozený defekt komorového septa | = en |
| uk | Рідкісна вроджена аномалія міжшлуночкової перегородки | Вроджена аномалія міжшлуночкової комунікації · Вроджена аномалія міжшлуночкової перегородки |
| zh | 罕见的先天性室间隔发育异常 | 先天性室间隔异常 |
| tr | Nadir doğumsal ventriküler septum anomalisi | Doğumsal ventriküler septal anomali · İnterventriküler iletimin doğumsal anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18771 | E | validated | |
| UMLS | C5680111 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:88991Rare congenital heart disease
rare developmental anomalies during embryogenesis; rare cardiac malformations
Codes that Orphanet moved or referred to this one:
- ORPHA:99096OBSOLETE: Multiple ventricular septal defects referred to · inactive
- ORPHA:99097OBSOLETE: Single ventricular septal defect 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/474347
- This record as JSON: /data/d/474347.json