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

Knobloch Syndrome | Hemophagocytic Lymphohistiocytosis | Woodhouse-Sakati Syndrome | Spinocerebellar Ataxia Type 17 | Adenoma, Pleomorphic | Familial Hemiplegic Migraine | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Diabetic Encephalopathy | Schindler Disease | Micro Syndrome | Seborrheic Dermatitis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | T-cell Prolymphocytic Leukemia | Achromatopsia | Anxiety Disorders | CEDNIK Syndrome | Focal Cortical Dysplasia Type 2 | Antisocial Personality Disorder | Mevalonate Kinase Deficiency | Intellectual Disability, Autosomal Dominant 5 | Cutaneous Angiosarcoma | 3-methylcrotonyl-CoA Carboxylase Deficiency | Cataract | Prolidase Deficiency | Incontinentia Pigmenti | Pathological Gambling | Nemaline Myopathy 8 | Celiac Disease | Kaposi Sarcoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Gnathodiaphyseal Dysplasia | Diabetes | Mucormycosis | ICF Syndrome | Juvenile Myoclonic Epilepsy | Brenner Tumor | Multiple Sclerosis | Hyperthyroidism | Neurodegeneration With Brain Iron Accumulation | CHARGE Syndrome | Ichthyosis, X-linked | Transcobalamin Deficiency | Basal Ganglia Disease | Shock, Cardiogenic | Gray Platelet Syndrome | Vitelliform Macular Dystrophy | Nicolaides-Baraitser Syndrome | Stomatitis | Hyperuricemic Nephropathy, Familial Juvenile | Reye Syndrome | Prolactinoma | Thalassemia, Beta | Schistosomiasis Mansoni | IgA Deficiency | Personality Disorders | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Dyskeratosis Congenita | Osteoarthritis | Spinocerebellar Ataxia Type 13 | Tuberculous Meningitis | Spinal Muscular Atrophy | Chylomicron Retention Disease | Thanatophoric Dysplasia Type 1 | Facioscapulohumeral Muscular Dystrophy Type 2 | Lymphoma, Mantle Cell | Infantile Liver Failure Syndrome 1 | Fontaine Progeroid Syndrome | Arterial Tortuosity Syndrome | Cirrhosis | Hypereosinophilic Syndrome | Keratoacanthoma | Alpha-mannosidosis | Congenital Disorders Of Glycosylation | Kawasaki Disease | Menkes Disease | Carbonic Anhydrase VA Deficiency | Craniofacial Dysostosis | Hypoparathyroidism | Cryptococcal Meningitis | Glaucoma, Congenital | Open-angle Glaucoma | Fibrosarcoma | Mitochondrial Encephalomyopathy | Melnick-Needles Syndrome | Meningitis | Stiff-man Syndrome | Malignant Peripheral Nerve Sheath Tumor | Fucosidosis | Paroxysmal Nocturnal Hemoglobinuria | Neurofibromatosis | Coronary Restenosis | Diffuse Palmoplantar Keratoderma | Anterior Segment Dysgenesis | Fibrodysplasia Ossificans Progressiva | Demyelinating Diseases | Myasthenia | Mesothelioma, Malignant | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Paroxysmal Kinesigenic Dyskinesia | Acute Leukemia | Fibromyalgia | Granular Corneal Dystrophy | Chylothorax, Congenital | Familial Cerebral Amyloid Angiopathy | Iron Overload | Ophthalmoplegia | Amenorrhea | Erythrokeratodermia Variabilis | Progressive Myoclonic Epilepsy | Glycogen Storage Disease Type 4 | Dystonia | Wieacker-Wolff Syndrome | Osteonecrosis | Carcinoma In Situ | Oligospermia | Carey-Fineman-Ziter Syndrome | Pneumonia, Mycoplasma | Pierpont Syndrome | Hyperhomocysteinemia | Pulmonary Sclerosing Hemangioma | Pelizaeus-Merzbacher Disease | Cerebellofaciodental Syndrome | Glutathione Synthetase Deficiency | Autonomic Neuropathy | Keratosis, Seborrheic | Cardiac Arrest | Hyperparathyroidism-jaw Tumor Syndrome | Nance-Horan Syndrome | Hypoplastic Left Heart Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Infectious Diarrhea | Charcot-Marie-Tooth Disease Type 4D | Corneal Neovascularization | Waardenburg Syndrome | Cardiomyopathy, Hypertrophic | Infantile Refsum Disease | Episodic Ataxia Type 1 | Maternally Inherited Diabetes And Deafness | Esophagitis, Eosinophilic | Danon Disease | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Down Syndrome | Dystonia-parkinsonism, X-linked | Fibrillation, Atrial | Gynecomastia | Diabetes Insipidus | Vitreoretinal Degeneration, Snowflake Type | Androgen Insensitivity | Autosomal Recessive Spastic Paraplegia Type 35 | Epidermolytic Ichthyosis, Annular | Adrenal Insufficiency | Hemangioma | Raine Syndrome | Thromboembolism | IgA Nephropathy | Myocardial Infarction | Central Retinal Artery Occlusion | Traboulsi Syndrome | Erdheim-Chester Disease | Renal-hepatic-pancreatic Dysplasia | Pemphigus Foliaceus | Cleidocranial Dysplasia | Stevens-Johnson Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Cancer, Brain | Conjunctivitis, Allergic | Peeling Skin Syndrome, Acral Type | Infantile Spasm | Rhabdomyosarcoma, Embryonal | Congenital Mirror Movements | Congenital Nystagmus | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Retinal Coloboma | Episodic Ataxia Type 2 | Sweet Syndrome | Prostatitis | Neurotoxicity | Dyslipidemia | Aneurysm, Abdominal Aortic | Intracranial Hypertension | Dentinogenesis Imperfecta | Alkaptonuria | Hypermethioninemia | Coffin-Lowry Syndrome | Acute Tubular Necrosis | Hoyeraal-Hreidarsson Syndrome | Hypertension, Essential | Ileitis | Milk Allergy | Epilepsy, Generalized | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Diabetic Nephropathy | Agoraphobia | Guttate Psoriasis | Phenylketonuria | Urethritis | Inflammatory Joint Disease | Metachromatic Leukodystrophy | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Chronic Beryllium Disease | Cold Agglutinin Disease | Endometritis | Fatty Aldehyde Dehydrogenase Deficiency | Pulmonary Veno-occlusive Disease | Leukoplakia | Nephropathy | Neovascular Glaucoma | Microphthalmia, Syndromic 7 | Palsy, Cerebral | Hypokalemia | Charcot-Marie-Tooth Disease, Type 2A | Usher Syndrome | Axenfeld-Rieger Syndrome | Renpenning Syndrome | Multiple Sclerosis, Chronic Progressive | HUPRA Syndrome | Non-proliferative Diabetic Retinopathy | Congenital Adrenal Hyperplasia 1 | Larsen Syndrome | Distal Myopathy 2 | Hereditary Folate Malabsorption | Absence Epilepsy | Hypophosphatemic Rickets, 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Disorder | Benign Recurrent Intrahepatic Cholestasis 1 | Neuroleptic Malignant Syndrome | Sick Sinus Syndrome | CREST Syndrome | Waardenburg Syndrome Type 4 | Campomelic Dysplasia | Erythromelalgia | Hemosiderosis | Charcot-Marie-Tooth Disease, Type 6 | Spinocerebellar Ataxia Type 8 | Necrotizing Autoimmune Myopathy | Neural Tube Defect | Spinocerebellar Ataxia Type 1 | Adrenomyeloneuropathy | Cohen Syndrome | Pityriasis Rubra Pilaris | Progressive External Ophthalmoplegia | Venous Insufficiency | Lymphoma Lymphoblastic | Protein C Deficiency | Congestive Heart Failure | Ocular Albinism Type 1 | Chronic Enteropathy Associated With SLCO2A1 Gene | Marfan Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Schnitzler Syndrome | Influenza | Neurofibromatosis-Noonan Syndrome | Spinocerebellar Ataxia Type 21 | Waardenburg Syndrome Type 2 | Bernard-Soulier Syndrome | Bainbridge-Ropers Syndrome | Trichorhinophalangeal Syndrome | Pituitary Dwarfism | Chronic Periodontitis | Hypotonia-cystinuria Syndrome | Cryopyrin-associated Periodic Syndromes | Macular Corneal Dystrophy | Nephronophthisis | Pulmonary Vein Stenosis | Wagner Disease | Smith-Lemli-Opitz Syndrome | Sialoadenitis | Delirium | Kallmann Syndrome | Central Core Disease | Early Infantile Epileptic Encephalopathy | Lymphomatoid Granulomatosis | Hyperoxaluria | DEND Syndrome | Bare Lymphocyte Syndrome | Congenital Torticollis | Diffuse Mesangial Sclerosis | Congenital Muscular Dystrophy | Keratosis | Megalencephaly | Neurogenic Bladder | Retinal Telangiectasia | Eating Disorder | Oculocutaneous Albinism | Follicular Dendritic Cell Sarcoma | Lymphoma | 3-methylglutaconic Aciduria Type I | Asthma, Nocturnal | Diabetes Mellitus, Transient Neonatal | Dermatitis | Microtia | Charcot-Marie-Tooth Disease Type 3 | Hyperparathyroidism, Secondary | ADNP Syndrome | Porencephaly | Poikiloderma With Neutropenia | Spastic Paraplegia Type 7 | Recurrent Respiratory Papillomatosis | Cyst | Nemaline Myopathy 10 | Leprosy | Osteochondrosis | Hyperinsulinism-hyperammonemia Syndrome | Ollier Disease | Chorioretinitis | Peyronie's Disease | Neonatal Progeroid Syndrome | Thyrotoxic Periodic Paralysis | Chronic Idiopathic Myelofibrosis | Rhabdomyosarcoma | Macular Corneal Dystrophy Type 1 | Chronic Granulomatous Disease | Cousin Syndrome | Methemoglobinemia Type IV | Scabies | Obesity | Myoclonus-dystonia Syndrome | Orotic Aciduria | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | L-2-Hydroxyglutaric Aciduria | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Chondrodysplasia Punctata | Spinal And Bulbar Muscular Atrophy | Lupus Erythematosus | Congenital Tufting Enteropathy | Spinocerebellar Ataxia Type 14 | Prader-Willi Syndrome | Autism Spectrum Disorders | Pupil Disorders | Ophthalmia, Sympathetic | Kabuki Syndrome | Acute Chest Syndrome | Shprintzen-Goldberg Syndrome | Temporal Lobe Epilepsy | Retinitis Pigmentosa 3 | Hemoglobinopathies | Congenital Dyserythropoietic Anemia Type 4 | Adenocarcinoma | Japanese Encephalitis | Trichotillomania | Multiple Sulfatase Deficiency | Sarcoidosis, Pulmonary | Scapuloperoneal Myopathy, X-linked Dominant | Galactosialidosis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Scleritis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Acute Generalized Exanthematous Pustulosis | Primary Sclerosing Cholangitis | Patent Ductus Arteriosus | Hartsfield Syndrome | Porphyria, Acute Intermittent | Facioscapulohumeral Muscular Dystrophy | Adenoma, Pituitary | Stroke, Ischemic | Porokeratosis | Left Ventricular Noncompaction | Tumoral Calcinosis | Infantile Nephropathic Cystinosis | Macrophage Activation Syndrome | Pulmonary Stenosis