raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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
LangNameSynonyms
enPelvic arteriovenous malformationArteriovenous malformation of the pelvis · Pelvic AVM
frMalformation artérioveineuse pelvienneMAV pelvienne · Malformation artérioveineuse du pelvis
deArteriovenöse Fehlbildung des BeckensArteriovenöse Malformation des Pelvis · AVM im Beckenbereich
esMalformación arteriovenosa pélvicaMAV pélvica · Malformación arteriovenosa de la pelvis
itMalformazione arterovenosa pelvicaAVM pelvica · Malformazione arterovenosa della pelvi · MAV pelvica · Malformazione arterovenosa del bacino
nlPelviene arterioveneuze malformatieArterioveneuze malformatie van bekken · Arterioveneuze malformatie van pelvis · Pelviene AVM
ptPelvic arteriovenous malformation
plMalformacja tętniczo-żylna miednicy= en
csPelvic arteriovenous malformation= en
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q27.8NTBTattributedvalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidatedORPHANET

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