Erythema Multiforme

About the Disease
Erythema Multiforme, also known as erythema polymorphe, erythema multiforme type, is related to severe cutaneous adverse reaction and graft-versus-host disease. An important gene associated with Erythema Multiforme is DSP (Desmoplakin), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Calcipotriol and Betamethasone have been mentioned in the context of this disorder. Affiliated tissues include skin, eye and salivary gland, and related phenotypes are no effect and no effect

Common Targets
HLA-B | HLA-A | HLA-DRA | HLA-C

Note: If you'd like to get a target analysis report for Erythema Multiforme, 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 Erythema Multiforme at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Neuromyelitis Optica | Diffuse Mesangial Sclerosis | Spinocerebellar Ataxia Type 23 | WAGR Syndrome | Antisynthetase Syndrome | Raynaud Phenomenon | Nicotine Addiction | Kabuki Syndrome | Dubin-Johnson Syndrome | Adenoma, Pituitary | Charcot-Marie-Tooth Disease Type 2T | Episodic Ataxia Type 2 | Cancer, Skin | Blepharospasm | Pneumonia, Viral | Reticular Dysgenesis | Schizophrenia, Paranoid | Myoclonus | Carcinoid Tumor | Meier-Gorlin Syndrome | Syphilis | Esophageal Motility Disorders | Dental Caries | Fibrillation, Atrial | Familial Retinal Arterial Macroaneurysm | Hereditary Spastic Paraplegia | Paraganglioma, Carotid Body | Pfeiffer Syndrome | Occipital Neuralgia | Danon Disease | Thrombophlebitis | Pseudoexfoliation Syndrome | Meesmann Corneal Dystrophy | Alcoholism | Macular Corneal Dystrophy Type 1 | Progressive Familial Intrahepatic Cholestasis Type 1 | Acrodermatitis | Protein C Deficiency | Williams Syndrome | Leukocyte Adhesion Deficiency | Stargardt Disease | Sensory Neuropathy | Waardenburg Syndrome Type 2E | Multifocal Motor Neuropathy | Focal Segmental Glomerulosclerosis | Insulinoma | Gray Platelet Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Microphthalmia | Ulcerative Colitis | Encephalopathy, Hepatic | Hyperuricemic Nephropathy, Familial Juvenile | Congenital Bilateral Absence Of Vas Deferens | Enhanced S-cone Syndrome | Usher Syndrome Type III | Lymphopenia | High Molecular Weight Kininogen Deficiency | Tietze Syndrome | Waardenburg Syndrome Type 2A | Sporadic Inclusion Body Myositis | Amblyopia | Left Ventricular Noncompaction | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Incontinentia Pigmenti | Renal Failure | Pseudohypoparathyroidism Type 2 | Lichen Sclerosus | Bare Lymphocyte Syndrome | Schizencephaly | Pleomorphic Xanthoastrocytoma | Pyruvate Decarboxylase Deficiency | Chondrosarcoma | Esophagitis | Irritable Bowel Syndrome | Ischemia | Ebstein Anomaly | Hypertensive Nephropathy | Autoimmune Hemolytic Anemia | Lysosomal Acid Lipase Deficiency | Canavan Disease | Keratosis | Methemoglobinemia Type IV | Heart Block | Angiosarcoma Of The Breast | Acute Leukemia | Herpes Simplex Dermatitis | Otitis Externa | Wieacker-Wolff Syndrome | Primary Hyperoxaluria | Babesiosis | Sarcoma, Alveolar Soft Part | Robinow Syndrome | Congenital Primary Aphakia | Pulmonary Alveolar Proteinosis | Facioscapulohumeral Muscular Dystrophy Type 2 | Lymphoma, B-cell | Lipid Metabolism Disorders | Vitamin B12 Deficiency | Trichothiodystrophy | Hypermetropia | Pulmonary Tuberculosis | Osteitis | Bietti Crystalline Dystrophy | Hypoplastic Left Heart Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Retinopathy Of Prematurity | Hydrolethalus Syndrome | Mitochondrial Encephalomyopathy | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Sclerosteosis 2 | Dyggve-Melchior-Clausen Disease | Spinocerebellar Ataxia Type 3 | Sezary Syndrome | Desbuquois Syndrome | Diabetes Type 1 | Wiedemann-Steiner Syndrome | Skin Papilloma | Specific Granule Deficiency | Wolfram Syndrome | Agoraphobia | Lissencephaly 2 | Gangliosidosis, GM1 | Synovitis | Cellulitis | Combined Pituitary Hormone Deficiency | Anal Fissure | Aspartylglycosaminuria | Autosomal Recessive Congenital Ichthyosis | Ectrodactyly | Enlarged Vestibular Aqueduct | Hennekam Lymphangiectasia-lymphedema Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Joubert Syndrome 2 | Stiff-man Syndrome | Carcinoma, Small Cell | Cabezas Syndrome | Carcinoma, Merkel Cell | Adenosine Deaminase 2 Deficiency | Urethritis | Glutaric Aciduria Type 2 | Epidermolytic Palmoplantar Keratoderma | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Charcot-Marie-Tooth Disease Type 3 | Kawasaki Disease | Diverticulitis | Optic Nerve Diseases | GAPO Syndrome | Basan Syndrome | Spermatocele | Wiskott-Aldrich Syndrome | Migraine | Spinocerebellar Ataxia Type 13 | Bernard-Soulier Syndrome | Celiac Disease | Waldenstrom Macroglobulinemia | Chediak-Higashi Syndrome | Parapsoriasis | Chromosome 5q Deletion Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hermansky-Pudlak Syndrome | Erythropoietic Protoporphyria | Nijmegen Breakage Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Hyperinsulinemia | Hyperinsulinemic Hypoglycemia | HIBCH Deficiency | Microcephaly | Bronchitis | Lattice Corneal Dystrophy Type 1 | Cardiomyopathy, Dilated, 1L | Intestinal Pseudo-obstruction | Lupus Erythematosus | T-cell Prolymphocytic Leukemia | Neutrophilia | Globozoospermia | Craniofrontonasal Syndrome | Hypopituitarism | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Acute Lymphocytic Leukemia | Hyperlipidemia Type V | Coronary Heart Disease | Melnick-Needles Syndrome | Fragile X Syndrome | Hereditary Spherocytosis | Hypoalbuminemia | Pseudohermaphroditism | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Papilledema | Gnathodiaphyseal Dysplasia | Amyotrophic Lateral Sclerosis, Juvenile | Salla Disease | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Dengue Shock Syndrome | X-linked Acrogigantism | Lipodystrophy | Hepatitis | Familial Hemiplegic Migraine | Congenital Nystagmus | Pulmonary Sclerosing Hemangioma | Cohen Syndrome | Osteoporosis-pseudoglioma Syndrome | Epidermolytic Ichthyosis, Annular | Pulmonary Capillary Hemangiomatosis | Crouzon Syndrome With Acanthosis Nigricans | Diabetic Neuropathy | Reflex Epilepsy | Heart Failure | Polymyositis | Cancer, Kidney | Combined Deficiency Of Factor V And Factor VIII | Cold Agglutinin Disease | Dermatomyositis | Erysipelas | Chromosome 17q21.31 Deletion Syndrome | Allergic Contact Dermatitis | Mixed Connective Tissue Disease | Sialoadenitis | Xeroderma Pigmentosum Variant Type | Cancer, Breast | Aldosterone Deficiency | Glycogen Storage Disease Type 1 | Optic Nerve Hypoplasia, Bilateral | Congenital Disorders Of Glycosylation Type II | Miyoshi Myopathy | Aneurysm, Abdominal Aortic | Moyamoya Disease | Congenital Nephrotic Syndrome | Sitosterolemia | Adrenoleukodystrophy, X-linked | Angina Pectoris | Meningioma, Benign | Creatine Deficiency Syndrome Due To AGAT Deficiency | Epithelial-myoepithelial Carcinoma | Dominant Optic Atrophy | Osteogenesis Imperfecta Type IV | Pseudohypoparathyroidism Type 1B | Sleep Apnea, Obstructive | Milk Allergy | Leiomyosarcoma | Iron Metabolism Disorders | Plasma Cell Leukemia | Stroke | Endometritis | Pemphigus Foliaceus | Sickle Cell Disease | Nutrition Disorders | Motor Neuron Diseases | Progressive Familial Intrahepatic Cholestasis Type 2 | Pemphigoid | Ichthyosis | Alkaptonuria | Cancer, Prostate | T-cell Lymphoma, Subcutaneous Panniculitis-like | Heroin Dependence | Combined Malonic And Methylmalonic Acidemia | Autosomal Recessive Bestrophinopathy | Glycogen Storage Disease Type 6 | Myotonic Disorders | Familial Dysautonomia | Tay-Sachs Disease | Congenital Central Hypoventilation Syndrome | Thin Basement Membrane Disease | Pyloric Stenosis, Infantile Hypertrophic | Portal Vein Thrombosis | Exocrine Pancreatic Insufficiency | Oculocutaneous Albinism | Malaria | Benign Hereditary Chorea | Trichuriasis | Esthesioneuroblastoma | Hyperthermia, Malignant | Ventricular Septal Defect | Otopalatodigital Syndrome Type 2 | Primary Hyperoxaluria Type 3 | Goiter | Uveitis, Anterior | Dyslipidemia | Tenosynovial Giant Cell Tumor | Meningeal Melanocytoma | Fetal Alcohol Syndrome | TARP Syndrome | Oculocutaneous Albinism Type 4 | Esophagitis, Eosinophilic | Hyperacusis | Hemochromatosis Type 2 | Achromatopsia | Vertebrobasilar Insufficiency | Lactose Intolerance | Kleine-Levin Syndrome | Apraxia | Progressive External Ophthalmoplegia | Intestinal Hypomagnesemia 1 | Pulverulent Zonular Cataract | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Porphyria, Variegate | Hyperprolactinemia | Toxic Epidermal Necrolysis | Waardenburg Syndrome Type 4A | Schnyder Crystalline Corneal Dystrophy | Stromal Corneal Dystrophy | Situs Inversus | Angioimmunoblastic T-cell Lymphoma | Juvenile Xanthogranuloma | FG Syndrome | Alzheimer Disease, Late Onset | Spondylosis | 3-hydroxy-3-methylglutaric Aciduria | Cutaneous Lupus Erythematosus | Pupil Disorders | Encephalopathy | Photosensitivity | Renal-hepatic-pancreatic Dysplasia | Asphyxia Neonatorum | Malnutrition | Acute Tubular Necrosis | Cystitis | Cartilage Disorders | ICF Syndrome | Skin Carcinoma | Acrocallosal Syndrome | Orthostatic Intolerance | Acanthosis Nigricans | Pendred Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Von Hippel-Lindau Disease | Congenital Torticollis | Charcot-Marie-Tooth Disease Type 4E | Atherosclerosis | Primary Ovarian Insufficiency | Huntington's Disease | Diabetes Insipidus, Nephrogenic | Keratosis, Actinic | Galactosialidosis | Deafness, Dystonia, And Cerebral Hypomyelination | Dystrophy, Cone-rod | Hyperinsulinism-hyperammonemia Syndrome | Trismus-pseudocamptodactyly Syndrome | Hyperlipidemia, Familial Combined | Nanophthalmos | Ocular Albinism Type 1 | Lassa Fever | Congenital Bile Acid Synthesis Defect | Peripheral Neuropathy | Pathological Gambling | Temporal Lobe Epilepsy | Fetal And Neonatal Alloimmune Thrombocytopenia | Auriculocondylar Syndrome | Dermatitis Herpetiformis | Niemann-Pick Disease | Chondromyxoid Fibroma | Erdheim-Chester Disease | Carotid Artery Disease | Rhabdomyosarcoma, Embryonal | Carbamoyl Phosphate Synthetase I Deficiency | Pierson Syndrome | Dysfibrinogenemia | Premature Ejaculation | Delirium | Peutz-Jeghers Syndrome | IgA Deficiency | Pearson Syndrome | Rett Syndrome | Retinoschisis | Progressive Myoclonic Epilepsy | Sialidosis Type I | Ovarian Hyperstimulation Syndrome | Cholangiocarcinoma | Stuttering | Vascular Calcification | Hypercholesterolemia, Familial | L-2-Hydroxyglutaric Aciduria | Intermittent Explosive Disorder | Transcobalamin Deficiency | Epicondylitis | Prolymphocytic Leukemia | Diabetic Macular Edema | Usher Syndrome Type II | Tetanus | Rift Valley Fever | Macrophage Activation Syndrome | Nager Acrofacial Dysostosis | Mesothelioma, Malignant | Antley-Bixler Syndrome | Budd-Chiari Syndrome | Tyrosinemia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spondyloarthritis | Dysgerminoma | Temtamy Preaxial Brachydactyly Syndrome | Cerebrotendinous Xanthomatosis | DNA Ligase IV Deficiency | Sporadic Hemiplegic Migraine | Mood Disorder | Focal Cortical Dysplasia Type 2 | Vasculitis | Atelosteogenesis Type 1 | Rhabdomyosarcoma, Alveolar | Priapism | Osteogenesis Imperfecta Type I | Tardive Dyskinesia