ORPHA:98722
Atrioventricular septal defect
Synonyms: AVSD · Atrioventricular canal defect
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Atrioventricular septal defect | AVSD · Atrioventricular canal defect |
| fr | Canal atrioventriculaire | Anomalie du canal atrioventriculaire · Anomalie du canal auriculo-ventriculaire · Communication atrioventriculaire · Communication auriculo-ventriculaire · Défaut du septum atrioventriculaire · Défaut septal atrioventriculaire · Défaut septal auriculo-ventriculaire |
| de | Atrioventrikulärer Septumdefekt | AV-Kanaldefekt · AVSD · Atrioventrikularkanaldefekt |
| es | Defecto de la comunicación auriculoventricular | AVSD · Defecto del canal auriculoventricular |
| it | Difetto del canale atrioventricolare | AVSD · Difetto del setto atrioventricolare |
| nl | Atrioventriculair septumdefect | AVSD · Defect van atrioventriculair kanaal |
| pt | Defeito do canal auriculoventricular | |
| pl | Kanał przedsionkowo-komorowy | AVSD · Wada przegrody przedsionkowo-komorowej |
| cs | Defekt atrioventrikulárního kanálu | AVSD · Atrioventrikulární septální defekt |
| uk | Атріовентрикулярна комунікація | Дефект атріовентрикулярного каналу · AVSD |
| zh | 房室间隔缺损 | 房室管缺损 |
| tr | Atriyoventriküler septal defekt | AVSD · Atriyoventriküler kanal defekti |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 606215 | BTNT | validated | |
| OMIM | 606217 | BTNT | validated | |
| OMIM | 614430 | BTNT | validated | |
| OMIM | 614474 | BTNT | validated | |
| OMIM | 615779 | BTNT | validated | |
| ICD-10 | Q21.2 | E | specific | validated |
| ICD-11 | LA87.4 | E | specific | validated |
| MeSH | C562831 | E | validated | |
| UMLS | C1389018 | E | validated | |
| GARD | 802 | E | validated | |
| MedDRA | 10063836 | 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 (2):
- ORPHA:98720Atrioventricular valve anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations - ORPHA:271853Genetic cardiac anomaly
rare genetic diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98722
- This record as JSON: /data/d/98722.json