Venezuelan equine encephalitis

disease
On this page

Also known as Venezuelan equine encephalitis virus caused disease or disorderVenezuelan equine encephalitis virus disease or disorderVenezuelan equine encephalitis virus infectious diseaseVenezuelan equine fever

Summary

Venezuelan equine encephalitis (MONDO:0006005) is a disease and 3 clinical trials. A subtype of encephalomyelitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameVenezuelan equine encephalitis
Mondo IDMONDO:0006005
EFOEFO:0007534
MeSHD004685
DOIDDOID:9584
ICD-10-CMA92.2
ICD-11608978790
NCITC35121
SNOMED CT417067005
UMLSC0014078
MedGen4036
GARD0006355
Is cancer (heuristic)no

Also known as: Venezuelan equine encephalitis virus caused disease or disorder · Venezuelan equine encephalitis virus disease or disorder · Venezuelan equine encephalitis virus infectious disease · Venezuelan equine fever

Disease family

This is a subtype of encephalomyelitis. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › nervous system disordercentral nervous system disorderencephalomyelitisVenezuelan equine encephalitis

Related subtypes (6): myelitis, cerebritis, optic neuritis, encephalitis, meningitis, hypophysitis

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE13

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07088822PHASE1NOT_YET_RECRUITINGA Phase 1 Study Evaluating the Safety, Tolerability, and Immunogenicity of V4020 Vaccine in Healthy Volunteers
NCT00109304PHASE1WITHDRAWNSafety, Tolerability and Immunogenicity of the Venezuelan Equine Encephalitis (VEE) Attenuated Live-Virus Vaccine
NCT03879603PHASE1COMPLETEDVRC 313: A Trivalent Virus-like Particle (VLP) Encephalitis Vaccine (WEVEE) in Healthy Adults

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.