ORPHA:271853
Genetic cardiac anomaly
- 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 | Genetic cardiac anomaly | |
| fr | Anomalie cardiaque d'origine génétique | |
| de | Herzanomalie, genetisch bedingte | |
| es | Anomalía cardíaca de origen genético | |
| it | Anomalia cardiaca genetica | |
| nl | Genetische hartanomalie | |
| pt | Anomalia cardíaca, genética | |
| pl | Wada serca uwarunkowana genetycznie | |
| cs | Geneticky podmíněné anomálie srdce | |
| uk | Генетично обумовлена серцева аномалія | |
| zh | 遗传性心脏异常 | |
| tr | Genetik kalp anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17131 | E | validated | |
| UMLS | C5680759 | 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:183530Rare genetic developmental defect during embryogenesis
rare genetic diseases
Children (12):
- ORPHA:98722Atrioventricular septal defect
- ORPHA:860Congenitally uncorrected transposition of the great arteries
- ORPHA:369891Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
- ORPHA:3426Double outlet right ventricle
- ORPHA:402075Familial bicuspid aortic valve
- ORPHA:741Familial mitral valve prolapse
- ORPHA:466729Familial patent arterial duct
- ORPHA:1478Interatrial communication
- ORPHA:566862Left isomerism
- ORPHA:97548Right isomerism
- ORPHA:101063Situs inversus totalis
- ORPHA:3193Supravalvular aortic stenosis
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/271853
- This record as JSON: /data/d/271853.json