Poliovirus infection

Summary

Poliovirus infection (MONDO:0024618) is a disease. A subtype of enterovirus 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	poliovirus infection
Mondo ID	MONDO:0024618
SNOMED CT	721764008
UMLS	C4303135
MedGen	928804
Is cancer (heuristic)	no

Also known as: Enterovirus C caused disease or disorder · Enterovirus C disease or disorder · Enterovirus C infectious disease · human poliovirus infection · infection caused by human poliovirus

Disease family

This is a subtype of enterovirus infectious disease. 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 etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › viral infectious disease › primary viral infectious disease › Picornaviridae infectious disease › enterovirus infectious disease › poliovirus infection

Related subtypes (5): coxsackievirus infectious disease, Echovirus infectious disease, congenital enterovirus infection, enterovirus antenatal infection, fetal enterovirus syndrome

Subtypes (2): poliomyelitis, meningitis caused by poliovirus

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.