Oropouche fever
disease diseaseOn this page
Also known as Oropouche virus caused disease or disorderOropouche virus disease or disorderOropouche virus infectious disease
Summary
Oropouche fever (MONDO:0000345) is a disease and 1 clinical trial. A subtype of Bunyaviridae infectious disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | Oropouche fever |
| Mondo ID | MONDO:0000345 |
| DOID | DOID:0050521 |
| ICD-10-CM | A93.0 |
| ICD-11 | 693244560 |
| SNOMED CT | 72880002 |
| UMLS | C0276386 |
| MedGen | 547314 |
| Is cancer (heuristic) | no |
Also known as: Oropouche virus caused disease or disorder · Oropouche virus disease or disorder · Oropouche virus infectious disease
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 › Bunyaviridae infectious disease › Oropouche fever
Related subtypes (2): hantavirus infectious disease, la Crosse encephalitis
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT07358910 | Not specified | RECRUITING | Risk Assessment of Community Spread of Multiple Endemic Infectious Diseases in a One Health Perspective |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.