ORPHA:714709
Mediastinal arteriovenous malformation
Synonyms: Arteriovenous malformation of the mediastinum · Mediastinal AVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mediastinal arteriovenous malformation | Arteriovenous malformation of the mediastinum · Mediastinal AVM |
| fr | Malformation artérioveineuse médiastinale | MAV médiastinale · Malformation artérioveineuse du médiastin |
| de | Mediastinale arteriovenöse Fehlbildung | Arteriovenöse Malformation des Mediastinums · Mediastinale AVM |
| es | Malformación arteriovenosa mediastínica | MAV mediastínica · Malformación arteriovenosa del mediastino |
| it | Malformazione arterovenosa mediastinica | Malformazione arterovenosa del mediastino · MAV mediastinica |
| nl | Mediastinale arterioveneuze malformatie | Arterioveneuze malformatie van mediastinum · Mediastinale AVM |
| pt | Mediastinal arteriovenous malformation | |
| pl | Malformacja tętniczo-żylna klatki śródpiersia | = en |
| cs | Mediastinal arteriovenous malformation | = en |
2
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.
3
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.
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 | <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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/714709
- This record as JSON: /data/d/714709.json