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

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Other Diseases

Central Core Disease | TARP Syndrome | Knobloch Syndrome | Angiosarcoma | Keratopathy | Inflammatory Linear Verrucous Epidermal Nevus | Cerebral Amyloid Angiopathy | Distal Myopathy 2 | Mastitis | Uremia | Fibromyalgia | Essential Fructosuria | Leiomyoma | Hyperuricemia | Acne Vulgaris | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Hemolytic Anemia | Generalized Epilepsy And Paroxysmal Dyskinesia | Syncope | Gerstmann-Straussler-Scheinker Syndrome | Treacher Collins Syndrome | Sotos Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Atopy | Ellis-Van Creveld Syndrome | 3C Syndrome | Oligodendroglioma | Syphilis | Iron Deficiency Anemia | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Polycystic Kidney, Autosomal Dominant | Chromosome 8q21.11 Deletion Syndrome | Diabetes Mellitus, Transient Neonatal | Cerebrovascular Disorders | Leukocyte Adhesion Deficiency Type 1 | Swine Influenza | Cornelia De Lange Syndrome | Anodontia | Non-proliferative Diabetic Retinopathy | Desbuquois Syndrome | Batten Disease | C3 Glomerulopathy | Acute Generalized Exanthematous Pustulosis | Corneal Dystrophy | Spinocerebellar Ataxia Type 38 | Usher Syndrome Type IIC | 3-methylglutaconic Aciduria Type IV | Ligneous Conjunctivitis | Migraine | Erythromelalgia | Amyotrophic Lateral Sclerosis | Malaria | Lymphangiomatosis | Harlequin Ichthyosis | Varicocele | Sclerosteosis 2 | Anovulation | Hypercalciuria | Congenital Adrenal Hyperplasia 1 | Adenoma, Pituitary | Colitis, Lymphocytic | Diabetes Type 1 | Hypophosphatasia | Benign Hereditary Chorea | Neural Tube Defect | Primary Hyperoxaluria | Fibrosarcoma | Paraganglioma | Hypopituitarism | Presbyopia | Primary Erythromelalgia | Thanatophoric Dysplasia Type 1 | Gardner Syndrome | Choroideremia | Urea Cycle Disorder | Mast Cell Leukemia | Meningococcal Meningitis | Pearson Syndrome | Pain | Tietze Syndrome | Renal Tubular Dysgenesis | Prurigo Nodularis | Glycogen Storage Disease Type 4 | Pseudo-pseudohypoparathyroidism | Vitreoretinal Degeneration, Snowflake Type | Sjogren Syndrome | Aneurysm, Thoracic Aortic | Alcoholism | Diverticulitis | Multiple System Atrophy | Actinomycetoma | Osteonecrosis Of The Jaw | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Growth Hormone Excess | Leukocyte Adhesion Deficiency | Loeys-Dietz Syndrome Type 4 | Chondrodysplasia Punctata 1, X-linked Recessive | Polymicrogyria | Thromboembolism | Porphyria, Acute Intermittent | Familial Exudative Vitreoretinopathy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Lattice Corneal Dystrophy | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | B-cell Chronic Lymphocytic Leukemia | Erysipelas | Gitelman Syndrome | NDH Syndrome | Hypothyroidism | Trigonocephaly | Isovaleric Acidemia | Hemorrhage | Tetanus | Delirium | Rhabdoid Tumor | Sarcoma | Hereditary Mixed Polyposis Syndrome | Melanoma, Uveal | Hypokalemic Periodic Paralysis | 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| Rubeosis Iridis | GLUT1 Deficiency Syndrome | Hemorrhoids | Galactosemia | Acrodermatitis | Tinea Versicolor | Tendinopathy | Mosaic Variegated Aneuploidy Syndrome 2 | Incontinentia Pigmenti | Xeroderma Pigmentosum | Neurofibroma | Bronchiectasis | Chromosome 5q Deletion Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Myositis, Focal | Intracerebral Hemorrhage | Congenital Sodium Diarrhea | Carotid Artery Disease | Seizures | Gingivitis | Facioscapulohumeral Muscular Dystrophy Type 2 | Stevens-Johnson Syndrome | Pleurisy | Riboflavin Transporter Deficiency Neuronopathy | Agammaglobulinemia | Craniofacial Dysostosis | Pseudohypoaldosteronism | Tinea | Currarino Syndrome | Gerodermia Osteodysplastica | Brachydactyly | Anorectal Fistula | Hereditary Hemorrhagic Telangiectasia | Oculocutaneous Albinism Type 4 | Nail Disorder, Nonsyndromic Congenital | Vaginitis | Vitamin D Deficiency | Facioscapulohumeral Muscular Dystrophy | Spinocerebellar Ataxia Type 20 | Deafness, Dystonia, And Cerebral Hypomyelination | Schuurs-Hoeijmakers Syndrome | Liver Diseases | Anti-NMDA Receptor Encephalitis | Syndactyly | Juvenile Myelomonocytic Leukemia | Angelman Syndrome | Primary Torsion Dystonia | Restless Legs Syndrome | Pendred Syndrome | Acute Leukemia | Periodic Limb Movement Disorder | Hyperlipidemia Type V | Leishmaniasis, Cutaneous | N-acetylglutamate Synthase Deficiency | GNE Myopathy | Chondrodysplasia Punctata 2, X-linked Dominant | Unverricht-Lundborg Syndrome | Glycogen Storage Disease Type 3 | Corneal Dystrophy And Perceptive Deafness | HUPRA Syndrome | Waardenburg Syndrome Type 2E | Gliosarcoma | Eiken Syndrome | Encephalopathy, Hepatic | Fanconi Syndrome | Rickets | Myofibromatosis | Anuria | Diabetes Insipidus, Nephrogenic | Spina Bifida | Paronychia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Retinopathy Of Prematurity | Hamartoma | Cantu Syndrome | Rash | Neuromyelitis Optica | Constipation | Usher Syndrome Type III | Epidermolytic Palmoplantar Keratoderma | Chronic Granulomatous Disease, X-linked | Carney Triad | Carey-Fineman-Ziter Syndrome | Retinal Coloboma | Blood Protein Disorders | Spondylo-ocular Syndrome | Olmsted Syndrome | Martsolf Syndrome | Cancer, Skin | Non-Langerhans Cell Histiocytosis | Peeling Skin Syndrome Type B | Ophthalmia, Sympathetic | Kidney Stones | Multiple Epiphyseal Dysplasia | HELLP Syndrome | Nephrotic Syndrome | Sporadic Hemiplegic Migraine | Asphyxia Neonatorum | Charcot-Marie-Tooth Disease Type 4B1 | Neuroendocrine Cancer | Peyronie's Disease | WAGR Syndrome | Botulism | Loeys-Dietz Syndrome | Campomelic Dysplasia | Cleidocranial Dysplasia | Epidermodysplasia Verruciformis | Leukoplakia, Oral | Wolff-Parkinson-White Syndrome | Benign Familial Neonatal Convulsions | Shprintzen-Goldberg Syndrome | Fundus Albipunctatus | Limb Girdle Muscular Dystrophy | Insulinoma | Sertoli Cell-only Syndrome | Goldenhar Syndrome | Myhre Syndrome | Osteochondroma | Acrodermatitis Enteropathica | Microcephaly | Imerslund-Grasbeck Syndrome | Glutathione Synthetase Deficiency | Early Infantile Epileptic Encephalopathy 28 | Charcot-Marie-Tooth Disease Axonal Type 2N | Whipple's Disease | Congenital Central Hypoventilation Syndrome | Avellino Corneal Dystrophy | Parkinsonism | Hemochromatosis | Alopecia | Renal Medullary Carcinoma | Cysticercosis | Inflammatory Bowel Disease | Poretti-Boltshauser Syndrome | Rolandic Epilepsy | Onchocerciasis | Lamellar Ichthyosis | Goiter | Myocardial Infarction | Charcot-Marie-Tooth Disease Type 2T | Kawasaki Disease | Pompe Disease | Osteomyelitis | Periventricular Nodular Heterotopia | Biotinidase Deficiency | Osteogenesis Imperfecta Type III | Pouchitis | Infantile Nephropathic Cystinosis | Atelosteogenesis Type 1 | Urolithiasis | Basan Syndrome | Persistent Truncus Arteriosus | Triple A Syndrome | Impulse Control Disorder | Dystonia Musculorum Deformans | Adenoma, Pleomorphic | Spondyloperipheral Dysplasia | Marfan Syndrome | Mevalonate Kinase Deficiency | Reticular Dysgenesis | Genee-Wiedemann Syndrome | Mohr-Tranebjaerg Syndrome | Camurati-Engelmann Disease | Aromatic L-amino Acid Decarboxylase Deficiency | Kabuki Syndrome 2 | Teratozoospermia | Eccrine Porocarcinoma | Panuveitis | Pulmonary Vein Stenosis | Sleep Disorder | Charcot-Marie-Tooth Disease, Type 2C | Lymphoma, AIDS-related | Meier-Gorlin Syndrome | Porokeratosis | Connective Tissue Disorders | Charcot-Marie-Tooth Disease | Majeed Syndrome | Osteoarthritis | Budd-Chiari Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Overactive Bladder | Pemphigus Vulgaris | Otopalatodigital Syndrome Type 2 | Vertebrobasilar Insufficiency | Superficial Spreading Melanoma | Endometrial Hyperplasia | Trimethylaminuria | Dermatitis Herpetiformis | Snyder-Robinson Syndrome | Alpers Syndrome | Nephrotic Syndrome Type 1 | Hypothalamic Obesity | Krabbe Disease | Canavan Disease | Chediak-Higashi Syndrome | Ganglioglioma | Binge Eating Disorder | Lymphangioma | Optic Nerve Hypoplasia, Bilateral | Protein C Deficiency | Primrose Syndrome | Esophageal Adenocarcinoma | Rheumatoid Arthritis | Osteoporosis | Kaposiform Hemangioendothelioma | Coronary Artery Disease | Erythema Multiforme | Sensory Neuropathy | Myoclonic Epilepsy With Ragged Red Fibers | Heterotaxy | Asthma, Exercise-induced | Combined Deficiency Of Factor V And Factor VIII | Skin Carcinoma | Enterocolitis, Necrotizing | Persistent Fetal Circulation | IMAGe Syndrome | Hypermetropia | Takotsubo Cardiomyopathy | Zollinger-Ellison Syndrome | Analgesia | Splenomegaly | Echinococcosis | Niemann-Pick Disease | Agranulocytosis | 5-oxoprolinase Deficiency | Thrombophlebitis | Alpha-mannosidosis | Retinal Diseases | Rhizomelic Chondrodysplasia Punctata | Glaucomatocyclitic Crisis | Hypertension | Neuroblastoma | Wiskott-Aldrich Syndrome | Heterotopic Ossification | Lipodystrophy | Polycystic Ovary Syndrome | Lichen Sclerosus | Encephalitis | Leishmaniasis, Visceral | Holt-Oram Syndrome | Infantile Liver Failure Syndrome 1 | Spinocerebellar Ataxia Type 21