ORPHA:98718
Aortic malformation
- Type
- Category
- 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 | Aortic malformation | |
| fr | Malformation aortique | |
| de | Aortenfehlbildung | |
| es | Malformación aórtica | |
| it | Malformazione aortica | |
| nl | Aortamalformatie | |
| pt | Malformação aórtica | |
| pl | Wada aorty | |
| cs | Aortální malformace | |
| uk | Мальформації аорти | |
| zh | 主动脉畸形 | |
| tr | Aort malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681689 | 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 (2):
- ORPHA:98724Congenital anomaly of the great arteries
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases - ORPHA:98717Transposition of the great arteries and conotruncal cardiac anomaly
rare developmental anomalies during embryogenesis; rare cardiac malformations
Children (8):
Codes that Orphanet moved or referred to this one:
- ORPHA:95449OBSOLETE: Congenital aortic valve insufficiency 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/98718
- This record as JSON: /data/d/98718.json