raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90078

Invasive infections due to vancomycin-resistant enterococci

Synonyms: Invasive infections due to VRE

Type
Particular clinical situation in a disease or syndrome
Group
Disorder
Age of onset
All ages
Status
active

A rare bacterial infectious disease characterized by invasive infection with vancomycin-resistant enterococci (VRE), typically after VRE colonization of the gastrointestinal tract or the skin in healthcare settings. Invasive infection most commonly occurs in immunocompromised individuals and patients with breaches in normal defensive barriers (such as intravascular lines or urinary catheters). Patients may develop urinary tract infection, bacteremia, and endocarditis, as well as infections of the abdomen, pelvis, biliary tract, and wounds. Less frequent infection sites include the bone, joints, and meninges, among others.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enInvasive infections due to vancomycin-resistant enterococciInvasive infections due to VRE
frInfection invasive par entérocoques résistants à la vancomycine
deInvasive Infektionen durch Vancomycin-resistente Enterokokken (VRE)
esInfecciones invasivas provocadas por enterococos resistentes a vancomicina (ERV)
itInfezioni invasive da enterococco resistente alla vancomicina (VRE)
nlInvasieve infecties als gevolg van vancomycineresistente enterokokkenInvasieve infecties als gevolg van VRE
ptInfeções invasivas provocadas por enterococos resistentes à vancomicina (VRE)
plInwazyjne zakażenie enterokokami opornymi na wankomycynęInwazyjne zakażenie VRE
csInvazivní infekce způsobená vankomycin-rezistentními enterokokyInvazivní infekce způsobená VRE
ukІнвазивні інфекції, спричинені стійкими до ванкоміцину ентерококамиІнвазивні інфекції, спричинені VRE
zh耐万古霉素所致肠球菌侵袭性感染VRE所致侵袭性感染
trVankomisine dirençli enterokoklara bağlı invazif enfeksiyonlarVRE'ye bağlı invazif enfeksiyonlar

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10A49.1NTBTattributedvalidated
ICD-111C4YNTBTattributedvalidated
UMLSC5680177Evalidated
MedDRA10053621Evalidated

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 prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

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.

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Sources for this card