Anomaly of the coronary ostia
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
A group of rare congenital coronary artery malformations comprising abnormal number of coronary ostia, malposition of a coronary ostium, and stenosis or atresia of a coronary ostium. Patients may remain asymptomatic or present with variable signs and symptoms, depending on the nature and severity of the malformation, including failure to thrive, dyspnea, syncope, angina pectoris, ventricular tachycardia, and myocardial ischemia.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Anomaly of the coronary ostia | |
| fr | Anomalie des ostia coronaires | |
| de | Anomalie des Koronarostium | |
| es | Anomalía de los ostia coronarios | |
| it | Anomalia degli osti coronarici | |
| nl | Anomalie van coronair ostium | |
| pt | Anomalia dos ostium coronários | |
| pl | Wada ujścia wieńcowego | |
| cs | Anomálie koronárního ostia | |
| uk | Аномалія коронарного отвору | |
| zh | 冠状动脉口异常 | |
| tr | Koroner ostia anomalisi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681322 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:1081Coronary artery congenital malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/542822
- This record as JSON: /data/d/542822.json