Erythema infectiosum

Summary

Erythema infectiosum (MONDO:0006544) is a disease. A subtype of viral exanthem — 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	erythema infectiosum
Mondo ID	MONDO:0006544
EFO	EFO:1000693
MeSH	D016731
DOID	DOID:8743
ICD-10-CM	B08.3
ICD-11	352375140
NCIT	C84695
SNOMED CT	34730008
UMLS	C0085273
MedGen	43142
Is cancer (heuristic)	no

Also known as: fifth disease

Disease family

Classification path: disease › human disease › disease by body system or component › integumentary system disorder › skin disorder › exanthem › viral exanthem › erythema infectiosum

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.