Exanthem
diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | exanthem |
| Mondo ID | MONDO:0006547 |
| EFO | EFO:1000697 |
| MeSH | D005076 |
| DOID | DOID:0050486 |
| SNOMED CT | 271807003 |
| UMLS | C0015230 |
| MedGen | 8732 |
| 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 disorder › exanthem
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.
| Drug | Development status |
|---|---|
| Hydrocortisone | Approved (phase 4) |
| Zinc Oxide | Approved (phase 4) |
Clinical trials & evidence
Clinical trials
Clinical trials: 20.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 9 |
| PHASE2 | 7 |
| PHASE1 | 2 |
| PHASE4 | 1 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01299220 | PHASE4 | WITHDRAWN | Study of Acitretin to Treat Skin Rash Caused by Erlotinib (a Chemotherapy Drug) |
| NCT01136005 | PHASE3 | COMPLETED | Bepanthen Versus Cetomacrogol in Epidermal Growth Factor Receptor Inhibitors (EGFRI) |
| NCT06399029 | PHASE2 | ACTIVE_NOT_RECRUITING | Topical Ruxolitinib Evaluation in Immune-related Lichenoid Skin-Toxicities |
| NCT00332163 | PHASE2 | COMPLETED | Skin Toxicity Treatment in Metastatic Colorectal Cancer (mCRC) Patients Receiving Panitumumab + Irinotecan-based Therapy |
| NCT00343187 | PHASE2 | TERMINATED | A Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlotinib)Related Rash |
| NCT00473083 | PHASE2 | COMPLETED | Systemic and Topical Treatments for Rash Secondary to Erlotinib in Lung Cancer |
| NCT00667589 | PHASE2 | TERMINATED | Sorafenib-induced Hand- Foot Skin Reaction Treatment |
| NCT01692626 | PHASE2 | TERMINATED | 1% Topical Pimecrolimus Cream for the Treatment of the Rash Associated With ERBITUX |
| NCT01880515 | PHASE2 | COMPLETED | Tetracycline as a Prophylaxis for Rash in Patients With NSCLC Receiving Treatment With BIBW2992 (Afatinib) |
| NCT02326467 | PHASE1 | COMPLETED | Pilot Study: Safety of Chlorhexidine (CHG) Baths in Patients Less Than 2 Months of Age |
| NCT05461456 | PHASE1 | COMPLETED | Bioavailability and Tolerability of Fexofenadine Hydrochloride Topical Lotion 1% |
| NCT06560853 | Not specified | ACTIVE_NOT_RECRUITING | Evaluation of a Comprehensive School Health Programme in Zambia |
| NCT07112846 | Not specified | NOT_YET_RECRUITING | Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections |
| NCT07476807 | Not specified | ENROLLING_BY_INVITATION | Telemedicine Rash Evaluation and Assessment of Toxicity in Skin in Acute Oncology and Haematology Care: A Pilot Study |
| NCT00610818 | Not specified | TERMINATED | Effect of Palifermin on Skin Tumors in Patients Undergoing Bone Marrow Transplantation |
| NCT00709878 | Not specified | COMPLETED | Histological Characterization and Differentiation of Rash From Other Epidermal Growth Factor Receptor (EGFR) Inhibitors |
| NCT01339546 | Not specified | COMPLETED | National Trends in Otitis Media in Children Under 5 Years of Age |
| NCT03102905 | Not specified | UNKNOWN | Prevalence 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? |
| NCT05247333 | Not specified | COMPLETED | Implementation of a Minor Ailment Service in Community Pharmacy Practice |
| NCT06755424 | Not specified | COMPLETED | GI Symptoms in Infants Fed Goat Milk-based Infant Formula |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CLINDAMYCIN | 4 | 3 |
| FEXOFENADINE | 4 | 3 |
| ACITRETIN | 4 | 1 |
| CHLORHEXIDINE GLUCONATE | 4 | 1 |
| DEXPANTHENOL | 4 | 1 |
| FLUOCINONIDE | 4 | 1 |
| MINOCYCLINE | 4 | 1 |
| PALIFERMIN | 4 | 1 |
| PANITUMUMAB | 4 | 1 |
| PIMECROLIMUS | 4 | 1 |
| TAZAROTENE | 4 | 1 |
| TETRACYCLINE | 4 | 1 |
| UREA | 4 | 1 |
| CHEMBL3775171 | 0 | 1 |
| CHEMBL4630645 | 0 | 1 |
| CHEMBL1628 | 0 | 1 |