Eosinophilic pustular folliculitis

Summary

Eosinophilic pustular folliculitis (MONDO:0023076) is a disease. A subtype of folliculitis — 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	eosinophilic pustular folliculitis
Mondo ID	MONDO:0023076
MeSH	C535953
ICD-11	1653155576
SNOMED CT	95333004
UMLS	C0406305
MedGen	140800
GARD	0008534
Is cancer (heuristic)	no

Also known as: eosinophilic folliculitis · eosinophilic folliculitis, pustular · EPF · Ofuji disease · Ofuji’s disease

Disease family

This is a subtype of folliculitis. 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 body system or component › integumentary system disorder › skin disorder › dermatitis › folliculitis › eosinophilic pustular folliculitis

Related subtypes (3): Demodex folliculitis, acne keloid, sycosis barbae

Subtypes (1): classic eosinophilic pustular folliculitis

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.