Pestivirus infectious disease
diseaseOn this page
Also known as infection, Pestivirusinfections, PestivirusPestivirus caused disease or disorderPestivirus disease or disorderPestivirus infection
Summary
Pestivirus infectious disease (MONDO:0005909) is a disease. A subtype of Flaviviridae infectious disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | pestivirus infectious disease |
| Mondo ID | MONDO:0005909 |
| EFO | EFO:0007432 |
| MeSH | D018182 |
| UMLS | C0206611 |
| MedGen | 60191 |
| Is cancer (heuristic) | no |
Also known as: infection, Pestivirus · infections, Pestivirus · Pestivirus caused disease or disorder · Pestivirus disease or disorder · Pestivirus infection · Pestivirus 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 › Flaviviridae infectious disease › pestivirus infectious disease
Related subtypes (9): Powassan encephalitis, Murray valley encephalitis, West Nile fever, dengue disease, st. Louis encephalitis, 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.