raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:693855

Visceral fast-flow vascular malformation

Synonyms: Arteriovenous malformation of internal organs · Visceral arteriovenous malformation

Type
Clinical group
Group
Group of disorders
Inheritance
Not applicable
Status
active

A group of rare fast-flow arteriovenous malformation characterized by abnormal communication between the arterial and the venous systems of the internal organs. They are more commonly observed in patients with multifocal vascular malformations. Clinical manifestations depend on the organ involved; however, they usually include abdominal pain, hemorrhage, chronic anemia, fatigue, gastrointestinal bleeding, hemoptysis and hypoxia.

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Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enVisceral fast-flow vascular malformationArteriovenous malformation of internal organs · Visceral arteriovenous malformation
frMalformation vasculaire viscérale à flux rapideMalformation artério-veineuse des organes internes · Malformation artério-veineuse viscérale
deViszerale schnell-fließende vaskuläre FehlbildungArteriovenöse Malformation der inneren Organe · Viszerale fast-flow vaskuläre Malformation · Viszerale arteriovenöse Malformation · Arteriovenöse Fehlbildung der inneren Organe
esMalformación vascular visceral de alto flujoMalformación arteriovenosa visceral · Malformación arteriovenosa de los órganos internos
itMalformazione vascolare viscerale a flusso rapidoMalformazione arterovenosa viscerale · Malformazione arterovenosa degli organi interni
nlViscerale fast-flow vasculaire malformatieArterioveneuze malformatie van inwendige organen · Viscerale vaatmalformatie met snelle bloedstroom · Viscerale arterioveneuze malformatie
ptMalformação arteriovenosa visceralMalformação arteriovenosa dos orgãos internos
plMalformacja tętniczo-żylna trzewna= en
csVisceral fast-flow vascular malformation= en

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (10):

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No prevalence record in this release.

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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