ORPHA:2041
Coronary arterial fistula
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Coronary arterial fistulas are a connection between one or more of the coronary arteries and a cardiac chamber or great vessel.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Coronary arterial fistula | |
| fr | Fistule coronaire | |
| de | Koronarfistel | |
| es | Fístula coronario-arterial | |
| it | Fistole delle arterie coronarie | Fistola coronarocardiaca · Malformazioni delle arterie coronarie |
| nl | Coronaire arteriële fistel | |
| pt | Fístula coronario-arterial | |
| pl | Przetoki tętnic wieńcowych | Malformacje tętnic wieńcowych · Przetoka wieńcowo-sercowa |
| cs | Vrozená píštěl věnčitých tepen | Koronární arteriální malformace · Koronární píštěle |
| uk | Фістула коронарної артерії | |
| zh | 冠状动脉瘘 | |
| tr | Koroner arter fistülü |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q24.5 | NTBT | attributed | validated |
| ICD-11 | LA8C.2 | E | specific | validated |
| MONDO | 0016081 | E | validated | |
| UMLS | C0265898 | E | validated | |
| GARD | 1533 | E | validated | |
| MedDRA | 10069441 | 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:1081Coronary artery congenital malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET_24940026[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
27 annotations · validated 2021-08-18| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0003115 | Abnormal EKG | |
| HP:0005162 | Abnormal left ventricular function | |
| HP:0001640 | Cardiomegaly | |
| HP:0001635 | Congestive heart failure | |
| HP:0031670 | Continuous heart murmur | |
| HP:0002875 | Exertional dyspnea | |
| HP:0031664 | Systolic heart murmur | |
| HP:0001649 | Tachycardia | |
| Occasional (29-5%) | ||
| HP:0001627 | Abnormal heart morphology | |
| HP:0001681 | Angina pectoris | |
| HP:0001650 | Aortic valve stenosis | |
| HP:0011675 | Arrhythmia | |
| HP:0001631 | Atrial septal defect | |
| HP:0006689 | Bacterial endocarditis | |
| HP:0001647 | Bicuspid aortic valve | |
| HP:0030882 | Coronary artery aneurysm | |
| HP:0002617 | Dilatation | |
| HP:0030848 | Elevated jugular venous pressure | |
| HP:0012764 | Orthopnea | |
| HP:0001962 | Palpitations | |
| HP:0001643 | Patent ductus arteriosus | |
| HP:0001655 | Patent foramen ovale | |
| HP:0010741 | Pedal edema | |
| HP:0002092 | Pulmonary arterial hypertension | |
| HP:0005133 | Right ventricular dilatation | |
| HP:0001279 | Syncope | |
| HP:0002789 | Tachypnea | |
Annotation source: 28740588[PMID]_30560560[PMID]_26381209[PMID]_30230248[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2041
- This record as JSON: /data/d/2041.json