ORPHA:714726
Retroperitoneal arteriovenous malformation
Synonyms: Arteriovenous malformation of the retroperitoneum · Retroperitoneal AVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Retroperitoneal arteriovenous malformation | Arteriovenous malformation of the retroperitoneum · Retroperitoneal AVM |
| fr | Malformation artérioveineuse rétropéritonéale | MAV rétropéritonéale · Malformation artérioveineuse du rétropéritoine |
| de | Retroperitoneale arteriovenöse Fehlbildung | Arteriovenöse Malformation des Retroperitoneums · Retroperitoneale AVM |
| es | Malformación arteriovenosa retroperitoneal | MAV retroperitoneal · Malformación arteriovenosa del retroperitoneo |
| it | Malformazione arterovenosa retroperitoneale | Malformazione arterovenosa del retroperitoneo · MAV retroperitoneale |
| nl | Retroperitoneale arterioveneuze malformatie | Arterioveneuze malformatie van retroperitoneum · Retroperitoneale AVM |
| pt | Retroperitoneal arteriovenous malformation | |
| pl | Malformacja tętniczo-żylna zaotrzewnowa | = en |
| cs | Retroperitoneal arteriovenous malformation | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q27.8 | NTBT | attributed | 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:714698Fast-flow vascular malformation of the thoraco-abdominal-pelvic cavity
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 30 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
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
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/714726
- This record as JSON: /data/d/714726.json