Exanthem

disease
On this page

Also known as cutaneous eruptionexanthem (disease)exanthemarashskin eruptionskin rash

Summary

Exanthem (MONDO:0006547) is a disease (an umbrella term covering 13 Mondo subtypes) and 20 clinical trials. Top therapeutic interventions include clindamycin, fexofenadine, and acitretin. A subtype of skin disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Umbrella term: 13 Mondo subtypes
  • Clinical trials: 20

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameexanthem
Mondo IDMONDO:0006547
EFOEFO:1000697
MeSHD005076
DOIDDOID:0050486
SNOMED CT271807003
UMLSC0015230
MedGen8732
Is cancer (heuristic)no

Also known as: cutaneous eruption · exanthem · exanthem (disease) · exanthema · rash · skin eruption · skin rash

Data availability: 1 HPO phenotype.

Disease family

This is a subtype of skin disorder. 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 disorderexanthem

Related subtypes (71): dermatitis, cutaneous mucinosis, skin neoplasm, pyoderma, chronic ulcer of skin, systemic sclerosis, sunburn, severe cutaneous adverse reaction, paronychia, Achenbach syndrome, erythema multiforme, erythematosquamous dermatosis, facial dermatosis, hand dermatosis, keratosis, leg dermatosis, lichen disease, lipodystrophy, mongolian spot, reactive cutaneous fibrous lesion, rosacea, scalp dermatosis, sebaceous gland disorder, skin atrophy, skin sarcoidosis, sweat gland disorder, vesiculobullous skin disease, hyperglobulinemic purpura, ainhum, cheilitis glandularis, erythema palmare hereditarium, multiple benign circumferential skin creases on limbs, actinic prurigo, congenital lethal erythroderma, Parana hard-skin syndrome, Bazex-Dupre-Christol syndrome, nephrogenic systemic fibrosis, erosive pustular dermatosis of the scalp, pseudoxanthoma elasticum-like papillary dermal elastolysis, toxic dermatosis, oral erosive lichen, chronic actinic dermatitis, Jessner lymphocytic infiltration of the skin, acquired kinky hair syndrome, primary cutaneous plasmacytosis, cutaneous pseudolymphoma, corticosteroid-sensitive aseptic abscess syndrome, interstitial granulomatous dermatitis with arthritis, epidermal disease, skin pigmentation disorder, skin vascular disease, Wells syndrome, solar urticaria, pellagra, hereditary epidermal appendage anomaly, keratosis pilaris, dermis disorder, aquagenic pruritus, Boudhina Yedes Khiari syndrome, non-neoplastic nevus, cutaneous sclerosis, pityriasis rotunda, hematohidrosis, skin disorder caused by infection, livedoid vasculopathy, prurigo nodularis, granuloma faciale, sclerema neonatorum, hereditary skin disorder, hand-foot syndrome, Nicolau syndrome

Subtypes (13): exanthema subitum, variola major infectious disease, pityriasis versicolor, bacterial exanthem, pityriasis rosea, viral exanthem, prurigo, pityriasis lichenoides, pityriasis simplex, pityriasis folliculorum, pityriasis amiantacea, pityriasis alba, pityriasis steatoides

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

Drugs indicated for this disease

2 approved. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
HydrocortisoneApproved (phase 4)
Zinc OxideApproved (phase 4)

Clinical trials & evidence

Clinical trials

Clinical trials: 20.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified9
PHASE27
PHASE12
PHASE41
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01299220PHASE4WITHDRAWNStudy of Acitretin to Treat Skin Rash Caused by Erlotinib (a Chemotherapy Drug)
NCT01136005PHASE3COMPLETEDBepanthen Versus Cetomacrogol in Epidermal Growth Factor Receptor Inhibitors (EGFRI)
NCT06399029PHASE2ACTIVE_NOT_RECRUITINGTopical Ruxolitinib Evaluation in Immune-related Lichenoid Skin-Toxicities
NCT00332163PHASE2COMPLETEDSkin Toxicity Treatment in Metastatic Colorectal Cancer (mCRC) Patients Receiving Panitumumab + Irinotecan-based Therapy
NCT00343187PHASE2TERMINATEDA Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlotinib)Related Rash
NCT00473083PHASE2COMPLETEDSystemic and Topical Treatments for Rash Secondary to Erlotinib in Lung Cancer
NCT00667589PHASE2TERMINATEDSorafenib-induced Hand- Foot Skin Reaction Treatment
NCT01692626PHASE2TERMINATED1% Topical Pimecrolimus Cream for the Treatment of the Rash Associated With ERBITUX
NCT01880515PHASE2COMPLETEDTetracycline as a Prophylaxis for Rash in Patients With NSCLC Receiving Treatment With BIBW2992 (Afatinib)
NCT02326467PHASE1COMPLETEDPilot Study: Safety of Chlorhexidine (CHG) Baths in Patients Less Than 2 Months of Age
NCT05461456PHASE1COMPLETEDBioavailability and Tolerability of Fexofenadine Hydrochloride Topical Lotion 1%
NCT06560853Not specifiedACTIVE_NOT_RECRUITINGEvaluation of a Comprehensive School Health Programme in Zambia
NCT07112846Not specifiedNOT_YET_RECRUITINGProspective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections
NCT07476807Not specifiedENROLLING_BY_INVITATIONTelemedicine Rash Evaluation and Assessment of Toxicity in Skin in Acute Oncology and Haematology Care: A Pilot Study
NCT00610818Not specifiedTERMINATEDEffect of Palifermin on Skin Tumors in Patients Undergoing Bone Marrow Transplantation
NCT00709878Not specifiedCOMPLETEDHistological Characterization and Differentiation of Rash From Other Epidermal Growth Factor Receptor (EGFR) Inhibitors
NCT01339546Not specifiedCOMPLETEDNational Trends in Otitis Media in Children Under 5 Years of Age
NCT03102905Not specifiedUNKNOWNPrevalence of Replication of Human Herpes Virus 6 (HHV6) in Blood and Skin During Exanthemia, in Patients With Hemopathy. Is There a Correlation With the Etiology of the Exanthema?
NCT05247333Not specifiedCOMPLETEDImplementation of a Minor Ailment Service in Community Pharmacy Practice
NCT06755424Not specifiedCOMPLETEDGI Symptoms in Infants Fed Goat Milk-based Infant Formula

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CLINDAMYCIN43
FEXOFENADINE43
ACITRETIN41
CHLORHEXIDINE GLUCONATE41
DEXPANTHENOL41
FLUOCINONIDE41
MINOCYCLINE41
PALIFERMIN41
PANITUMUMAB41
PIMECROLIMUS41
TAZAROTENE41
TETRACYCLINE41
UREA41
CHEMBL377517101
CHEMBL463064501
CHEMBL162801