st. Louis encephalitis
disease diseaseOn this page
Also known as Neuroinvasive St. Louis encephalitis virus infectionSaint Louis encephalitisSt. Louis encephalitis virus caused infectious encephalitisSt. Louis encephalitis virus infectious encephalitis
Summary
st. Louis encephalitis (MONDO:0005969) is a disease. A subtype of Flaviviridae infectious disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Worldwide)
Clinical features
Epidemiology
Prevalence records
1 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.38 | Europe | Not yet validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | st. Louis encephalitis |
| Mondo ID | MONDO:0005969 |
| EFO | EFO:0007495 |
| MeSH | D004674 |
| Orphanet | 83484 |
| DOID | DOID:10845 |
| ICD-10-CM | A83.3 |
| ICD-11 | 1306878274 |
| SNOMED CT | 417607009 |
| UMLS | C0014060 |
| MedGen | 41773 |
| GARD | 0019041 |
| MedDRA | 10041896 |
| Is cancer (heuristic) | no |
Also known as: Neuroinvasive St. Louis encephalitis virus infection · Saint Louis encephalitis · St. Louis encephalitis virus caused infectious encephalitis · St. Louis encephalitis virus infectious encephalitis
Disease family
Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › viral infectious disease › primary viral infectious disease › Flaviviridae infectious disease › st. Louis encephalitis
Related subtypes (9): Powassan encephalitis, Murray valley encephalitis, West Nile fever, dengue disease, pestivirus infectious disease, Kyasanur forest disease, Omsk hemorrhagic fever, Zika virus infectious disease, yellow fever
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: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.