Peripheral arteriovenous fistula
Synonyms: Peripheral AVF
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
A rare fast-flow vascular anomaly characterized by direct extracranial artery-to-vein communication without an intervening nidus. The majority of the cases are asymptomatic. When present, the symptoms may include fatigue, dyspnea, palpitations, congestive heart failure, and pulmonary hypertension.
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Peripheral arteriovenous fistula | Peripheral AVF |
| fr | Fistule artérioveineuse périphérique | AVF périphérique |
| de | Periphere arteriovenöse Fistel | Periphere AVF |
| es | Fístula arteriovenosa periférica | FAV periférica |
| it | Fistola arterovenosa periferica | AVF periferica · FAV periferica congenita |
| nl | Perifere arterioveneuze fistel | Perifere AVF |
| pt | Peripheral arteriovenous fistula | |
| pl | Wrodzona przetoka tętniczo-żylna obwodowa | = en |
| cs | Peripheral arteriovenous fistula | = en |
Definition in:
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.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:707944Peripheral fast-flow vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/708051
- This record as JSON: /data/d/708051.json