ORPHA:99089
Abnormal number of coronary ostia
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Abnormal number of coronary ostia | |
| fr | Anomalie de nombre des ostia coronaires | |
| de | Koronarostium, abnormale Anzahl | |
| es | Número anómalo de los ostia coronarios | |
| it | Numero anomalo di osti coronarici | |
| nl | Abnormaal aantal coronaire ostia | |
| pt | Óstio coronário, anomalia de número | |
| pl | Nieprawidłowa liczba ujść wieńcowych | |
| cs | Abnormální počet koronárních ostií | |
| uk | Аномальна кількість вусть коронарних артерій | |
| zh | 冠状窦口数目异常 | |
| tr | Anormal sayıda koroner osti |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q24.5 | NTBT | attributed | validated |
| ICD-11 | LA8C.Y | NTBT | attributed | validated |
| MONDO | 0020425 | E | validated | |
| UMLS | C5191081 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:542822Anomaly of the coronary ostia
rare developmental anomalies during embryogenesis; rare cardiac malformations
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/99089
- This record as JSON: /data/d/99089.json