ORPHA:714715
Pelvic arteriovenous malformation
Synonyms: Arteriovenous malformation of the pelvis · Pelvic AVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pelvic arteriovenous malformation | Arteriovenous malformation of the pelvis · Pelvic AVM |
| fr | Malformation artérioveineuse pelvienne | MAV pelvienne · Malformation artérioveineuse du pelvis |
| de | Arteriovenöse Fehlbildung des Beckens | Arteriovenöse Malformation des Pelvis · AVM im Beckenbereich |
| es | Malformación arteriovenosa pélvica | MAV pélvica · Malformación arteriovenosa de la pelvis |
| it | Malformazione arterovenosa pelvica | AVM pelvica · Malformazione arterovenosa della pelvi · MAV pelvica · Malformazione arterovenosa del bacino |
| nl | Pelviene arterioveneuze malformatie | Arterioveneuze malformatie van bekken · Arterioveneuze malformatie van pelvis · Pelviene AVM |
| pt | Pelvic arteriovenous malformation | |
| pl | Malformacja tętniczo-żylna miednicy | = en |
| cs | Pelvic 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| 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/714715
- This record as JSON: /data/d/714715.json