ORPHA:1081
Coronary artery congenital 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 | Coronary artery congenital malformation | |
| fr | Anomalie congénitale des artères coronaires | |
| de | Fehlbildung der Koronararterien, kongenitale | |
| es | Anomalía congénita de arterias coronarias | |
| it | Anomalia congenita delle coronarie | |
| nl | Kransslagader congenitale misvorming | |
| pt | Malformação congénita das artérias coronárias | |
| pl | Wrodzona malformacja tętnic wieńcowych | |
| cs | Vrozená malformace koronárních tepen | |
| uk | Вроджена вада розвитку коронарних артерій | |
| zh | 冠状动脉先天畸形 | |
| tr | Koroner arter doğumsal malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q24.5 | E | specific | validated |
| ICD-11 | LA8C | E | specific | validated |
| MONDO | 0015203 | E | validated | |
| MONDO | 15203 | E | validated | |
| UMLS | C0158623 | E | validated | |
| GARD | 1534 | E | validated | |
| MedDRA | 10061060 | 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
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/1081
- This record as JSON: /data/d/1081.json