ORPHA:707944

Peripheral fast-flow vascular malformation

Synonyms: Peripheral arteriovenous malformation

Type: Clinical group
Group: Group of disorders
Status: active

A group of rare fast-flow arteriovenous malformation characterized by variable appearance and symptoms, located in the head and neck region, the limbs, the chest and the trunk. The group includes both arteriovenous malformations and arteriovenous fistulas.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	Peripheral fast-flow vascular malformation	Peripheral arteriovenous malformation
fr	Malformation vasculaire périphérique à flux rapide	Malformation artério-veineuse périphérique
de	Periphere schnell-fließende vaskuläre Fehlbildung	Periphere fast-flow vaskuläre Malformation
es	Malformación vascular periférica de alto flujo	Malformación arteriovenosa periférica
it	Malformazione vascolare periferica a flusso rapido	Malformazione arterovenosa periferica
nl	Perifere fast-flow vasculaire malformatie	Perifere arterioveneuze malformatie · Perifere vaatmalformatie met snelle bloedstroom
pt	Peripheral fast-flow vascular malformation or fistula
pl	Obwodowa malformacja naczyniowa lub przetoką o szybkim przepływie	= en
cs	Peripheral fast-flow vascular malformation	= en

Definition in:

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:715762Unifocal fast-flow vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases

Children (4):

Codes that Orphanet moved or referred to this one:

ORPHA:141168OBSOLETE: Frontonasal arteriovenous malformation referred to · inactive
ORPHA:141171OBSOLETE: Maxillary arteriovenous malformation referred to · inactive
ORPHA:141174OBSOLETE: Mandibular arteriovenous malformation referred to · inactive
ORPHA:156230OBSOLETE: Facial arteriovenous malformation referred to · inactive

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/707944
This record as JSON: /data/d/707944.json