O'nyong'nyong fever

disease
On this page

Also known as O'nyong-nyong virus caused disease or disorderO'nyong-nyong virus disease or disorderO'nyong-nyong virus infectious disease

Summary

O’nyong’nyong fever (MONDO:0000342) is a disease. A subtype of Alphavirus 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

FieldValue
Canonical nameO’nyong’nyong fever
Mondo IDMONDO:0000342
DOIDDOID:0050516
ICD-10-CMA92.1
SNOMED CT85579005
UMLSC0276286
MedGen547234
GARD0027520
Is cancer (heuristic)no

Also known as: O’nyong-nyong virus caused disease or disorder · O’nyong-nyong virus disease or disorder · O’nyong-nyong virus infectious disease

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious diseaseviral infectious disease › primary viral infectious disease › Togaviridae infectious disease › Alphavirus infectious disease › O’nyong’nyong fever

Related subtypes (5): Barmah forest virus disease, Ross river fever, Venezuelan equine encephalitis, chikungunya, western equine 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: 0.

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