ORPHA:101043
Congenital aortic valve dysplasia
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Congenital aortic valve stenosis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital aortic valve dysplasia | |
| fr | Dysplasie valvulaire aortique congénitale | |
| de | Aortenklappendysplasie, kongenitale | |
| es | Displasia de la válvula aórtica congénita | |
| it | Displasia aortica valvolare | |
| nl | Congenitale dysplasie van aortaklep | |
| pt | Displasia da válvula aórtica | |
| pl | Dysplazja zastawki aorty | |
| cs | Dysplázie aortální chlopně | |
| uk | Вроджена дисплазія аортального клапана | |
| zh | 先天性主动脉瓣发育不良 | |
| tr | Doğumsal aort kapak displazisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q23.0 | NTBT | attributed | validated |
| UMLS | C5397239 | E | validated | |
| GARD | 19776 | 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:3093Congenital aortic valve stenosis
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
No children.
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/101043
- This record as JSON: /data/d/101043.json