Dermatitis

disease
On this page

Also known as inflammation of skininflammation of the skininflammation of zone of skininflammatory skin diseaseskin inflammationzone of skin inflammation

Summary

Dermatitis (MONDO:0002406) is a disease (an umbrella term covering 33 Mondo subtypes) with 88 GWAS associations across 33 studies and 89 clinical trials. Top therapeutic interventions include cephalexin anhydrous, clemastine, and fexofenadine. 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: 33 Mondo subtypes
  • GWAS associations: 88
  • ClinVar variants: 1
  • Clinical trials: 89

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namedermatitis
Mondo IDMONDO:0002406
MeSHD003872
DOIDDOID:2723
NCITC2983
SNOMED CT43116000
UMLSC3875321
MedGen849741
Is cancer (heuristic)no

Also known as: inflammation of skin · inflammation of the skin · inflammation of zone of skin · inflammatory skin disease · skin inflammation · zone of skin inflammation

Data availability: 1 ClinVar variant · 88 GWAS associations (33 studies) · 1 cell line.

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 disorderdermatitis

Related subtypes (71): cutaneous mucinosis, skin neoplasm, pyoderma, chronic ulcer of skin, systemic sclerosis, sunburn, severe cutaneous adverse reaction, paronychia, Achenbach syndrome, erythema multiforme, erythematosquamous dermatosis, exanthem, 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 (33): spongiotic dermatitis, atopic eczema, psoriasis, contact dermatitis, urticaria, acneiform dermatitis, acrodermatitis, folliculitis, granuloma annulare, granulomatous dermatitis, lichen planus, neurodermatitis, neurotic excoriation, parapsoriasis, pityriasis rosea, seborrheic dermatitis, acanthosis nigricans, dermatosis papulosa nigra, lichen sclerosus et atrophicus, vitiligo, acne, porphyria cutanea tarda, dermatomyositis, acute generalized exanthematous pustulosis, hydroa vacciniforme, autoimmune bullous skin disease, cutaneous vasculitis, skin infection, intertrigo, lipodermatosclerosis, exfoliative dermatitis, radiodermatitis, food dermatitis

Genetics & variants

GWAS landscape

88 GWAS associations across 33 studies. Top hits map to 17 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
chr1:1523133859e-85A0.41
rs618396603e-45IL2RAC0.14
chr10:60527349e-38T0.15
chr17:406082724e-28A0.21
chr6:326346195e-27T0.08
chr6:322434414e-24G0.06
rs18075445e-21CSF2RBC0.05
rs10483725e-21HLA-DQA1T0.09
chr20:637049064e-18T0.06
chr5:1326602724e-18G0.08
chr5:358528136e-18G0.06
chr1:1523075474e-17A1.91
chr6:1590855684e-17T0.05
chr2:1116014781e-16G0.05
chr22:373195891e-16G0.05
rs6967343e-16CAPSLA0.05
chr11:765910298e-16A0.06
chr11:765881509e-16T0.05
rs66724204e-15RUNX3A0.04
rs101833383e-14ACOXLG0.05
chr6:1594975976e-14C0.06
chr16:111295977e-14G0.05
chr16:111357329e-14C0.04
chr11:1283174881e-13C0.05
chr11:364284473e-13C0.13
rs100606153e-13SLC22A5T0.04
chr17:388694905e-13A0.17
rs121238216e-13CCDSTC0.11
rs100758018e-13MIR3936HG, SLC22A4A0.04
rs79314839e-13EMSY - LINC02757C0.04

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90473917UK Biobank Whole-Genome Sequencing Consortium202570,720387,720Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667885UK Biobank Whole-Genome Sequencing Consortium202570,720387,720Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90476289Verma A202466,194325,245Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90473933UK Biobank Whole-Genome Sequencing Consortium202546,037412,403Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667906UK Biobank Whole-Genome Sequencing Consortium202546,037412,403Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90479306Verma A202419,55786,442Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480627Verma A202419,55786,442Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90726714Kim HI202613,00431,022Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.
GCST90077853Backman JD202112,790318,964Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90081839Backman JD202112,790318,964Exome sequencing and analysis of 454,787 UK Biobank participants.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding2
Tier 2: splice/UTR1
Tier 3: regulatory1
Tier 4: intronic/intergenic46

MAF distribution

BucketVariants
common (>=0.05)18
low_freq (0.01-0.05)5
rare (<0.01)1
unknown26

Functional consequences

ConsequenceCount
unknown33
intron_variant11
stop_gained1
missense_variant1
non_coding_transcript_exon_variant1
3_prime_UTR_variant1
regulatory_region_variant1
intergenic_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
chr1:1523133859e-85Tier 4: intronic/intergenic
rs61839660106052734C>T0.094intron_variantIL2RA3e-45Tier 4: intronic/intergenic
chr10:60527349e-38Tier 4: intronic/intergenic
chr17:406082724e-28Tier 4: intronic/intergenic
chr6:326346195e-27Tier 4: intronic/intergenic
chr6:322434414e-24Tier 4: intronic/intergenic
rs18075442236915177C>A,T0.453intron_variantCSF2RB5e-21Tier 4: intronic/intergenic
rs1048372632642659T>A,C,G0.46stop_gainedHLA-DQA15e-21Tier 1: coding
chr20:637049064e-18Tier 4: intronic/intergenic
chr5:1326602724e-18Tier 4: intronic/intergenic
chr5:358528136e-18Tier 4: intronic/intergenic
chr1:1523075470.0054e-17Tier 4: intronic/intergenic
chr6:1590855684e-17Tier 4: intronic/intergenic
chr2:1116014780.361e-16Tier 4: intronic/intergenic
chr22:373195890.4541e-16Tier 4: intronic/intergenic
rs696734535928406A>C,T0.272intron_variantCAPSL3e-16Tier 4: intronic/intergenic
chr11:765910298e-16Tier 4: intronic/intergenic
chr11:765881509e-16Tier 4: intronic/intergenic
rs6672420124964519A>C,G,T0.488missense_variantRUNX34e-15Tier 1: coding
rs101833382110853239G>A,T0.293intron_variantACOXL3e-14Tier 4: intronic/intergenic
chr6:1594975970.1276e-14Tier 4: intronic/intergenic
chr16:111295977e-14Tier 4: intronic/intergenic
chr16:111357329e-14Tier 4: intronic/intergenic
chr11:1283174881e-13Tier 4: intronic/intergenic
chr11:364284470.0263e-13Tier 4: intronic/intergenic
rs100606155132373185T>A,C0.467intron_variantSLC22A53e-13Tier 4: intronic/intergenic
chr17:388694900.035e-13Tier 4: intronic/intergenic
rs121238211152206676C>T0.047intron_variantCCDST6e-13Tier 4: intronic/intergenic
rs100758015132341949A>G0.377intron_variantMIR3936HG, SLC22A48e-13Tier 4: intronic/intergenic
rs79314831176591023C>A,G0.448non_coding_transcript_exon_variantEMSY - LINC027579e-13Tier 4: intronic/intergenic

ClinVar germline variants

1 retrieved; paginated sample, class counts are floors:

1 pathogenic

ClinVarVariant (HGVS)GeneClassificationReview
26804446;XX;ins(2;9)(q24.3;p22.1p24.3)dnPathogeniccriteria provided, single submitter

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

7 approved, 8 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
Betamethasone AcetateApproved (phase 4)
DexamethasoneApproved (phase 4)
DimethiconeApproved (phase 4)
HydrocortisoneApproved (phase 4)
Methylprednisolone AcetateApproved (phase 4)
Triamcinolone AcetonideApproved (phase 4)
Zinc OxideApproved (phase 4)
BepotastinePhase 3 (in late-stage trials)
CetirizinePhase 3 (in late-stage trials)
ClemastinePhase 3 (in late-stage trials)
DesloratadinePhase 3 (in late-stage trials)
DupilumabPhase 3 (in late-stage trials)
KetoconazolePhase 3 (in late-stage trials)
LevocetirizinePhase 3 (in late-stage trials)
PimecrolimusPhase 3 (in late-stage trials)

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Acitretin, Apremilast, Crisaborole, Risankizumab, Roflumilast, Sulfamethoxazole, Trimethoprim.

Clinical trials & evidence

Clinical trials

Clinical trials: 89.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified55
PHASE211
PHASE310
PHASE15
PHASE43
PHASE1/PHASE23
PHASE2/PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06750653PHASE4RECRUITINGSkin Barrier Function and Inflammation in Aging: The BIA Study
NCT00667056PHASE4COMPLETEDStudy of the Safety and Efficacy of Tacrolimus Ointment in Treating Chronic Allergic Contact Dermatitis
NCT05324618PHASE4COMPLETEDTacrolimus Versus Hydrocortisone in Atopic Dermatitis
NCT05535738PHASE2/PHASE3ACTIVE_NOT_RECRUITINGUsing a Contact Dermatitis Model With Biologic Medications to Study Skin Inflammation
NCT00176956PHASE3TERMINATEDAtopic Dermatitis-Like Skin Disease in Pediatric Heart Transplant Patients
NCT00375713PHASE3COMPLETEDRandomized Phase III Study to Evaluate the Efficacy and Safety of Xyzal® (Levocetirizine) vs Zyrtec® (Cetirizine) in Subjects With Dermatitis and Eczema
NCT01125761PHASE3WITHDRAWNEfficacy and Safety of the Association Drugs in Patients With Allergic Dermatitis
NCT01239719PHASE3UNKNOWNRandomized Study for Effectiveness and Safety Evaluation of Dexamethasone 0.5 mg + Fumarate Clemastine 1 mg Compared to Dexamethasone 0.5 mg in Patients With Allergic Dermatitis
NCT01762020PHASE3COMPLETEDBarrier Film vs. Standard Skin Care in Preventing Dermatitis in Women With Breast Cancer Receiving Radiation
NCT01840605PHASE3COMPLETEDA Confirmatory Study of TAU-284 in Pediatric Patients With Atopic Dermatitis
NCT01916980PHASE3COMPLETEDEfficacy and Safety Study of Desloratadine (MK-4117) in Japanese Participants With Eczema/Dermatitis and Dermal Pruritus (MK-4117-202)
NCT03627767PHASE3COMPLETEDStudy to Investigate Efficacy and Safety of PF-04965842 in Subjects Aged 12 Years and Over With Moderate to Severe Atopic Dermatitis With the Option of Rescue Treatment in Flaring Subjects
NCT03720470PHASE3COMPLETEDStudy Evaluating Efficacy and Safety of PF-04965842 and Dupilumab in Adult Subjects With Moderate to Severe Atopic Dermatitis on Background Topical Therapy
NCT04760314PHASE3COMPLETEDA Study of Lebrikizumab (LY3650150) in Combination With Topical Corticosteroids in Japanese Participants With Moderate-to-Severe Atopic Dermatitis
NCT01631617PHASE2RECRUITINGEffects of Treatments on Atopic Dermatitis
NCT07011706PHASE2ACTIVE_NOT_RECRUITINGATI-045 Versus Placebo in Patients With Moderate-to-Severe Atopic Dermatitis
NCT07599813PHASE2RECRUITINGA Phase 2b Study of the Effects of Camoteskimab in Adults With Moderate-to-Severe Atopic Dermatitis
NCT00421161PHASE1/PHASE2UNKNOWNOlive Oil With Omega 3 to Treat Stasis Dermatitis
NCT00746382PHASE2WITHDRAWNA Placebo Controlled 4 Week Proof of Concept Study With 0.5% Roflumilast Cream in Patients With Mild Atopic Dermatitis (RO-2351-001-EM)
NCT02580279PHASE2UNKNOWNStudy of Epigallocatechin-3-gallate (EGCG) for Skin Prevention in Patients With Breast Cancer Receiving Adjuvant Radiotherapy
NCT03563066PHASE2COMPLETEDEffect of Benralizumab in Atopic Dermatitis
NCT03706040PHASE2COMPLETEDA Study to Evaluate Risankizumab in Adults and Adolescents With Moderate to Severe Atopic Dermatitis
NCT03976206PHASE1/PHASE2WITHDRAWNVery Small Embryonic-like Stem Cells for Facial Skin Antiaging
NCT04154033PHASE2WITHDRAWNTreatment of Chronic Itch in Atopic Dermatitis With Topical Naltrexone
NCT04325802PHASE2WITHDRAWNTreatment of Chronic Itch in Atopic Dermatitis With Opioid Antagonist Naltrexone
NCT04479514PHASE2COMPLETEDPreventative Skin Care for Children Undergoing Targeted CNS Tumor Therapy
NCT05104723PHASE1/PHASE2COMPLETEDSafety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications
NCT06436183PHASE2COMPLETEDA Study of the Effects of Camoteskimab in Adults With Moderate to Severe Atopic Dermatitis
NCT07414602PHASE1RECRUITINGA Phase I Study of Single Subcutaneous Dose of SHR-1894 in Healthy Subjects
NCT01259323PHASE1COMPLETEDSequential Ascending Dose Study to Assess the Safety and Tolerability of REGN668 (SAR231893) in Patients With Atopic Dermatitis
NCT01910662PHASE1COMPLETEDCharacterisation of T-cell Response to Keyhole Limpet Hemocyanin (KLH) and Tuberculin Purified Protein Derivative (PPD)
NCT02447393PHASE1COMPLETEDPhase 1 Study of Levocetirizine
NCT05461456PHASE1COMPLETEDBioavailability and Tolerability of Fexofenadine Hydrochloride Topical Lotion 1%
NCT00217009EARLY_PHASE1TERMINATEDStudy to Compare Different Light Therapies (Narrowband Ultraviolet B vs PUVA) for Hand and Foot Skin Diseases.
NCT03024671Not specifiedRECRUITINGEpicutaneous Testing of Cosmetics for Skin Compatibility
NCT05611346Not specifiedRECRUITINGHYPNOsis in the Management of Atopic Dermatitis in Children and Teenagers
NCT06353087Not specifiedRECRUITINGAbrocitinib Taiwan Treatment Pattern and Real World Study in ATopiC Dermatitis (ATTRACT Registry)
NCT06448702Not specifiedNOT_YET_RECRUITINGEvaluation of Efficacy and Safety of Enhanced External Counter-pulsation on Patients With Atopic Dermatitis and Inflammatory Skin Disease Requiring Wet Wrap Therapy
NCT06794671Not specifiedNOT_YET_RECRUITINGA Basket Trial of Vunakizumab in Inflammatory Skin Diseases
NCT06850389Not specifiedRECRUITINGPMCF Investigation of Medical Device ChitoCare® Medical

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CEPHALEXIN ANHYDROUS43
CLEMASTINE43
FEXOFENADINE43
TACROLIMUS ANHYDROUS43
ABROCITINIB42
BEPOTASTINE42
CETIRIZINE42
DUPILUMAB42
LEVOCETIRIZINE42
BENRALIZUMAB41
BETAMETHASONE VALERATE41
CANAKINUMAB41
DESLORATADINE41
GUSELKUMAB41
HYDROCORTISONE41
KETOTIFEN FUMARATE41
LEBRIKIZUMAB41
OLIVE OIL41
RISANKIZUMAB41
ROFLUMILAST41
SARILUMAB41
SODIUM HYPOCHLORITE41
TOFACITINIB41
TRIMETHOPRIM41
USTEKINUMAB41
TUBERCULIN31
CAMOTESKIMAB22
SQUARIC ACID DIBUTYL ESTER21
CHEMBL456492301
CHEMBL25910001