raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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
LangNameSynonyms
enMediastinal arteriovenous malformationArteriovenous malformation of the mediastinum · Mediastinal AVM
frMalformation artérioveineuse médiastinaleMAV médiastinale · Malformation artérioveineuse du médiastin
deMediastinale arteriovenöse FehlbildungArteriovenöse Malformation des Mediastinums · Mediastinale AVM
esMalformación arteriovenosa mediastínicaMAV mediastínica · Malformación arteriovenosa del mediastino
itMalformazione arterovenosa mediastinicaMalformazione arterovenosa del mediastino · MAV mediastinica
nlMediastinale arterioveneuze malformatieArterioveneuze malformatie van mediastinum · Mediastinale AVM
ptMediastinal arteriovenous malformation
plMalformacja tętniczo-żylna klatki śródpiersia= en
csMediastinal 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