Herpes Simplex Dermatitis

About the Disease
Eczema Herpeticum, also known as herpes simplex eyelid dermatitis, is related to molluscum contagiosum and blepharitis, and has symptoms including watery blisters, fever and swelling of the lymph nodes. An important gene associated with Eczema Herpeticum is ADSS2 (Adenylosuccinate Synthase 2), and among its related pathways/superpathways are Innate Immune System and Keratinization. The drugs Meticillin and Omalizumab have been mentioned in the context of this disorder. Affiliated tissues include skin, t cells and bone marrow, and related phenotypes are immune system and hematopoietic system

Common Targets
IFNGR1 | TGM2

Note: If you'd like to get a target analysis report for Herpes Simplex Dermatitis, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Herpes Simplex Dermatitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Pneumonia, Bacterial | Anosmia, Congenital | Tinea | Van Der Knaap Disease | Still Disease | Spina Bifida | Optic Nerve Hypoplasia, Bilateral | Sporadic Hemiplegic Migraine | Sepiapterin Reductase Deficiency | Neurodevelopmental Disorders | Amish Infantile Epilepsy Syndrome | Cavitary Optic Disc Anomalies | Zellweger Syndrome | Endometrial Hyperplasia | Hidradenitis | Transient Bullous Dermolysis Of The Newborn | Takenouchi-Kosaki Syndrome | Micropenis | Spinal And Bulbar Muscular Atrophy | Sjogren Syndrome | Blepharo-cheilo-odontic Syndrome | Waardenburg Syndrome Type 2 | Enhanced S-cone Syndrome | Disseminated Superficial Actinic Porokeratosis | Intestinal Hypomagnesemia 1 | T-cell Lymphoma, Subcutaneous Panniculitis-like | Familial Retinal Arterial Macroaneurysm | Spinocerebellar Ataxia Type 7 | IgA Nephropathy | Distal Myopathy | Cryptosporidiosis | Camptocormia | Leukocyte Adhesion Deficiency Type 1 | Tularemia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Hydrocephalus, Normal Pressure | Nephronophthisis | Arthritis | Craniometaphyseal Dysplasia | Proximal Symphalangism | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Diabetes | Richter's Syndrome | Crisponi Syndrome | Glycogen Storage Disease Type 0 | Blastomycosis | Specific Granule Deficiency | Keratosis, Seborrheic | Calcium Pyrophosphate Deposition Disease | Stiff-man Syndrome | Delayed Sleep Phase Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Uterine Leiomyoma | Mitochondrial Cytopathy | Pulmonary Sclerosing Hemangioma | Camurati-Engelmann Disease | Mast Cell Leukemia | Infertility | Erythematotelangiectatic Rosacea | Williams Syndrome | CDKL5 Deficiency Disorder | Arthritis, Reactive | Cabezas Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Rickets | Epilepsy Of Infancy With Migrating Focal Seizures | Miyoshi Myopathy | Tremor | Bartter Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Glycogen Storage Disease Type 1b | Osteoporosis, Postmenopausal | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Hashimoto Thyroiditis | Acrodysostosis | Mesothelioma, Malignant | Plasma Cell Dyscrasia | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Cerebrotendinous Xanthomatosis | Familial Dysautonomia | Steel Syndrome | Primary Hyperoxaluria Type 3 | Rheumatoid Arthritis | Potocki-Shaffer Syndrome | Primary Sclerosing Cholangitis | Dystonia | Hypotrichosis | Birk-Barel Syndrome | Congenital Torticollis | Frank-ter Haar Syndrome | Marshall-Smith Syndrome | Schnitzler Syndrome | Microcephalic Primordial Dwarfism | Anovulation | Anthrax | Achondrogenesis | Epilepsy | Endocarditis | Hypercholesterolemia | Prader-Willi Syndrome | Hemolytic Anemia | Chronic Leukemia | Johanson-Blizzard Syndrome | Alexander Disease | Chediak-Higashi Syndrome | Multicystic Renal Dysplasia | Seizures-scoliosis-macrocephaly Syndrome | Spinocerebellar Ataxia Type 10 | Bare Lymphocyte Syndrome | Evans Syndrome | Macular Corneal Dystrophy | Osteomalacia | Peripheral Neuropathy | Non-Hodgkin Lymphoma | Sulfite Oxidase Deficiency | Rubeosis Iridis | Brugada Syndrome 1 | Astigmatism | Bainbridge-Ropers Syndrome | Polycystic Ovary Syndrome | Klippel-Feil Syndrome | Auriculocondylar Syndrome | LEOPARD Syndrome | Common Variable Immunodeficiency | Autosomal Recessive Bestrophinopathy | Facioscapulohumeral Muscular Dystrophy Type 1 | Familial Cerebral Amyloid Angiopathy | Hypereosinophilic Syndrome | Japanese Encephalitis | Cerebral Cavernous Malformations | Thyroid Dyshormonogenesis | Acromicric Dysplasia | Phosphoglycerate Dehydrogenase Deficiency | Rhizomelic Chondrodysplasia Punctata | Renal Hypouricemia | Fuchs Dystrophy | Glycogen Storage Disease Type 5 | Leber Congenital Amaurosis | Prolidase Deficiency | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Temporal Lobe Epilepsy | Hyperuricemia | Glomerulonephritis, Membranoproliferative | Renal Hypomagnesemia 3 | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Vertebrobasilar Insufficiency | Ovarian Sex Cord-stromal Tumor | Osteoglophonic Dysplasia | Pseudohypoparathyroidism Type 2 | Niemann-Pick Disease | Stevens-Johnson Syndrome | Oculodentodigital Dysplasia | Seminoma | Exfoliative Dermatitis | Muckle-Wells Syndrome | Leukocyte Adhesion Deficiency | Microvillus Inclusion Disease | Myelofibrosis | Duane Retraction Syndrome | Schistosomiasis Mansoni | Birt-Hogg-Dube Syndrome | Gastric Atrophy | Malignant Peripheral Nerve Sheath Tumor | Proteasome-associated Autoinflammatory Syndrome 2 | Primary Biliary Cholangitis | Rosacea | Noonan Syndrome-like Disorder With Loose Anagen Hair | Congenital Disorders Of Glycosylation Type II | Beare-Stevenson Syndrome | Cenani-Lenz Syndactyly Syndrome | Ophthalmia, Sympathetic | Cardiac Sarcoidosis | Choriocarcinoma | Retinitis Pigmentosa | Sertoli Cell-only Syndrome | Essential Fructosuria | Hyperparathyroidism | Hypermetropia | Down Syndrome | Hyperhomocysteinemia | Liver Diseases | Pelizaeus-Merzbacher Disease | Thrombophlebitis | Pleomorphic Xanthoastrocytoma | Lattice Corneal Dystrophy Type 1 | Short-chain Acyl-CoA Dehydrogenase Deficiency | Peeling Skin Syndrome Type B | Polycystic Liver | Spinocerebellar Ataxia Type 6 | Androgen Insensitivity | Desbuquois Syndrome | Thrombasthenia | Motor Neuron Diseases | Renal Tubular Acidosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Nevus | Asthma | Autism | Gnathodiaphyseal Dysplasia | Cockayne Syndrome | Acrodermatitis | Hypertensive Retinopathy | Allergic Contact Dermatitis | Vitamin K Deficiency | Leri-Weill Dyschondrosteosis | Thin Basement Membrane Disease | Intermittent Claudication | Lyme Disease | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Vitamin D Deficiency | Epidermolytic Ichthyosis, Annular | Metanephric Adenoma | Syphilis | Cherubism | IgA Deficiency | Waldenstrom Macroglobulinemia | Idiopathic Pulmonary Fibrosis | Neurofibromatosis Type 2 | Gout | Mucormycosis | Sialoadenitis | Prostatitis | Pemphigoid | Myoclonic Epilepsy With Ragged Red Fibers | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pulmonary Vein Stenosis | Supravalvular Aortic Stenosis | Pregnancy, Ectopic | Ichthyosis, X-linked | Urea Cycle Disorder | Heimler Syndrome | Cri-du-chat Syndrome | Pulmonary Stenosis | Hypophosphatasia | Apraxia | Angina Pectoris | 3-hydroxy-3-methylglutaric Aciduria | Pneumoconiosis | Bronchiolitis | Rett Syndrome | Leishmaniasis, Cutaneous | Aceruloplasminemia | Thrombotic Microangiopathy | Benign Hereditary Chorea | Rash | Cantu Syndrome | Tic Disorder | Hypertrophy | Oculocutaneous Albinism Type 1 | Small Lymphocytic Lymphoma | Conjunctivitis | Pure Red Cell Aplasia | Polycystic Kidney, Autosomal Recessive | Antenatal Bartter Syndrome Type 1 | Glutaric Aciduria Type 3 | Vitiligo | Neurocutaneous Melanocytosis | Hepatitis D | Blastoma, Pleuropulmonary | Charcot-Marie-Tooth Disease Type 2T | Precocious Puberty | Multiple Sclerosis, Relapsing-remitting | Graft-versus-host Disease | Argininosuccinic Aciduria | Insulin Resistance | Hypospadias | Spinocerebellar Ataxia Type 12 | Hypertension, Essential | Light Chain Amyloidosis | Urofacial Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Vitamin B12 Deficiency | Nasodigitoacoustic Syndrome | Cysticercosis | Pyruvate Dehydrogenase Deficiency | McKusick Type Metaphyseal Chondrodysplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Hepatic Veno-occlusive Disease | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Spondylolisthesis | Inflammatory Bowel Disease | Bronchitis | Sickle Cell Disease | Early Infantile Epileptic Encephalopathy 1 | Gastroenteritis, Eosinophilic | Becker Muscular Dystrophy | Long QT Syndrome Type 1 | Spondyloperipheral Dysplasia | Ghosal Syndrome | Primary Cutaneous Amyloidosis | Charcot-Marie-Tooth Disease Type 4D | Histiocytosis | Adult Polyglucosan Body Disease | Chorea | Dermatitis | Congenital Dysfibrinogenemia | Adenocarcinoma | Heart Failure | Kashin-Beck Disease | Syncope | Synpolydactyly | Retinitis Pigmentosa 3 | Hyperbilirubinemia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Encephalocele | Primary Progressive Nonfluent Aphasia | Blepharophimosis Syndrome | Adenoma, Villous | Vertigo | Dowling-Degos Disease | Stuve-Wiedemann Syndrome | Alazami Syndrome | Esophageal Motility Disorders | Norrie Disease | Polycythemia Vera | Neuromyelitis Optica | CHOPS Syndrome | Diabetes Insipidus, Nephrogenic | Hepatitis, Autoimmune | Meningitis | Intermittent Explosive Disorder | Tetraplegia | Hyperthermia, Malignant | Liver Failure, Acute Infantile | Dementia, Vascular | X-linked Myotubular Myopathy | Aneurysm, Thoracic Aortic | Fatty Aldehyde Dehydrogenase Deficiency | Varices | Juvenile Myelomonocytic Leukemia | Congenital Hereditary Endothelial Dystrophy Type I | Keratitis | Gardner Syndrome | Eating Disorder | Echinococcosis | Poretti-Boltshauser Syndrome | Fascioliasis | Angioedema, Hereditary | Microcephaly, Seizures, And Developmental Delay | Geleophysic Dysplasia | ICF Syndrome | Eosinophilic Asthma | Primary Familial Brain Calcification | Wieacker-Wolff Syndrome | Carney Triad | Spinocerebellar Ataxia Type 21 | Fibrodysplasia Ossificans Progressiva | Central Pain Syndrome | Scleritis | Methemoglobinemia Type IV | Split Hand-foot Malformation | Porphyria, Acute Intermittent | Hereditary Mixed Polyposis Syndrome | Perivascular Epithelioid Cell Tumor | Progressive External Ophthalmoplegia | Sclerosteosis 2 | Arrhythmogenic Right Ventricular Cardiomyopathy | Spinocerebellar Ataxia Type 3 | Hyperammonemia | Charcot-Marie-Tooth Disease Type 4 | Congenital Adrenal Hyperplasia | Diabetes Gestational | Oral Lichen Planus | Myasthenia Gravis | Familial Isolated Hyperparathyroidism | Glioblastoma | Cholangitis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Glycogen Storage Disease Type 6 | Hepatitis, Alcoholic | Antiphospholipid Syndrome | Dominant Optic Atrophy | Neurodegeneration With Brain Iron Accumulation | Diabetic Nephropathy | Fragile X Syndrome | Corneal Dystrophy And Perceptive Deafness | Antisocial Personality Disorder | Vici Syndrome | Empyema | Thromboembolism | Macular Degeneration | Restrictive Dermopathy | Anal Fissure | Sorsby Fundus Dystrophy | Filariasis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Treacher Collins Syndrome | Oligospermia | WAGR Syndrome | Polyarteritis Nodosa | Tardive Dyskinesia | Antley-Bixler Syndrome | Retinal Vasculitis | Uveitis, Anterior | Crohn's Disease | Endometriosis | Gingivitis | Mixed Connective Tissue Disease | Schizencephaly | Enlarged Vestibular Aqueduct