Erysipelas
Erysipelas
About the Disease
Erysipelas is related to erysipeloid and fasciitis, and has symptoms including exanthema An important gene associated with Erysipelas is TNF (Tumor Necrosis Factor), and among its related pathways/superpathways are Innate Immune System and Spinal cord injury. The drugs Phenoxymethylpenicillin and Vancomycin have been mentioned in the context of this disorder. Affiliated tissues include skin, lymph node and breast, and related phenotypes are no effect and no effect
Common Targets
F3 | MEFV

Note: If you'd like to get a target analysis report for Erysipelas, 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 Erysipelas at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Pulmonary Alveolar Proteinosis | Guttate Psoriasis | Purpura, Thrombotic Thrombocytopenic | Cancer, Lung | Carpal Tunnel Syndrome | Congenital Stromal Corneal Dystrophy | Deafness, Dystonia, And Cerebral Hypomyelination | Coronary Artery Disease | Gastroenteritis | Necrotizing Autoimmune Myopathy | Cheilitis | Leukoplakia, Oral | Gaucher Disease | Dementia, Vascular | Epidermolysis Bullosa Simplex | Pneumococcal Meningitis | Loeys-Dietz Syndrome Type 4 | Leprosy | Odonto-onycho-dermal Dysplasia | Cancer, Kidney | Thrombophilia | Osteoporosis, Postmenopausal | Perivascular Epithelioid Cell Tumor | Exfoliative Dermatitis | Iron Metabolism Disorders | Carey-Fineman-Ziter Syndrome | Polycystic Kidney, Autosomal Recessive | Spinocerebellar Ataxia Type 13 | Progressive External Ophthalmoplegia | Congestive Heart Failure | Rhizomelic Chondrodysplasia Punctata | Infantile Spasm | Autism Spectrum Disorders | Rhabdomyosarcoma | Arthritis | Alzheimer Disease, Late Onset | Hypolipoproteinemia | Lattice Corneal Dystrophy Type 1 | Idiopathic Multicentric Castleman Disease | Hypotension, Orthostatic | Cold Agglutinin Disease | Reye Syndrome | Episodic Ataxia | GM2-gangliosidosis AB Variant | Early Infantile Epileptic Encephalopathy | Epidermolysis Bullosa | Mevalonate Kinase Deficiency | Myoclonic Epilepsy With Ragged Red Fibers | Platelet Disorders | Rickets | Acne Vulgaris | Cardiac Sarcoidosis | Renal Tubular Acidosis | Stroke | VACTERL/VATER Association | Congenital Disorders Of Glycosylation | Osteonecrosis | Chondrosarcoma | Intracranial Hypertension | X-linked Acrogigantism | Ataxia-ocular Apraxia 2 | Microcephalic Primordial Dwarfism | Spinocerebellar Ataxia Type 31 | Hypogonadism | Choroiditis | Pure Red Cell Aplasia | Hereditary Sensory And Autonomic Neuropathy | Chordoid Glioma | Lassa Fever | 3-hydroxy-3-methylglutaric Aciduria | Wolcott-Rallison Syndrome | Carcinoid Tumor | Autoimmune Autonomic Ganglionopathy | Epiphyseal Chondrodysplasia, Miura Type | Hypokalemic Periodic Paralysis | Tetraplegia | Panic Disorder | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Dent Disease | Esophagitis, Eosinophilic | Desmosterolosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Precocious Puberty | Guillain-Barre Syndrome | Microphthalmia | Multiple Sclerosis | Agranulocytosis | D-2-Hydroxyglutaric Aciduria | Spinocerebellar Ataxia Type 14 | Atelosteogenesis Type 1 | Juvenile Myoclonic Epilepsy | Addison Disease | Seizures | Recurrent Respiratory Papillomatosis | Connective Tissue Disorders | Partington Syndrome | Congenital Torticollis | Trichorhinophalangeal Syndrome | Antenatal Bartter Syndrome Type 1 | Arterial Tortuosity Syndrome | Avian Influenza | Myeloid Leukemia | Spastic Paraplegia Type 7 | Amyotrophic Lateral Sclerosis, Juvenile | Cutaneous T-cell Lymphoma | Dystonia-parkinsonism, X-linked | Schaaf-Yang Syndrome | Pterygium | Glycogen Storage Disease Type 9 | Axenfeld-Rieger Syndrome | Blepharoconjunctivitis | Babesiosis | Bardet-Biedl Syndrome | Thyroiditis, Autoimmune | Sick Sinus Syndrome 1 | Glycogen Storage Disease Type 3 | Pachyonychia Congenita | Antisocial Personality Disorder | Keratosis | DEND Syndrome | Endometritis | Carney Triad | Hepatitis E | Sensorineural Hearing Loss | Saethre-Chotzen Syndrome | Fraser Syndrome | Congenital Poikiloderma | Mandibuloacral Dysplasia With Type A Lipodystrophy | Macrophagic Myofasciitis | Chondromyxoid Fibroma | Interstitial Lung Diseases | Carcinoma In Situ | Neuromuscular Disorders | Globozoospermia | Angiosarcoma | Dermatofibrosarcoma | Allan-Herndon-Dudley Syndrome | Mitochondrial DNA Depletion Syndrome | Nephrotic Syndrome | Familial Male-limited Precocious Puberty | Poikiloderma With Neutropenia | Celiac Disease | Mucolipidosis | Sialoadenitis | Autoimmune Polyendocrine Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Mountain Sickness | Seasonal Mood Disorder | Klinefelter Syndrome | Pulverulent Zonular Cataract | Hepatorenal Syndrome | Osteoporosis-pseudoglioma Syndrome | Familial Cerebral Amyloid Angiopathy | Venous Insufficiency | Distal Myopathy 2 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Oligoastrocytoma | Cardiofaciocutaneous Syndrome | Lymphangioleiomyomatosis | Familial Dysautonomia | Persistent Mullerian Duct Syndrome | Osteitis | Osteomyelitis | Periodic Limb Movement Disorder | Primary Carnitine Deficiency | Arthritis, Gouty | Stuve-Wiedemann Syndrome | Glycogen Storage Disease Type 1a | Myelodysplasia | Erythromelalgia | Netherton Syndrome | Chromosome 8q21.11 Deletion Syndrome | Encephalopathy, Glycine | Macular Degeneration | Pseudohypoparathyroidism Type 1C | Mucolipidosis Type III | Fanconi Anemia | Chondrodysplasia Punctata | Malonyl-CoA Decarboxylase Deficiency | Dyslexia | Autosomal Recessive Spastic Paraplegia Type 75 | Tyrosinemia Type 2 | Schindler Disease | Photosensitivity | Multifocal Motor Neuropathy | Binge Eating Disorder | Cystitis | Corneal Dystrophies, Hereditary | Glycogen Storage Disease Type 5 | Motor Neuron Diseases | Klippel-Feil Syndrome | Cenani-Lenz Syndactyly Syndrome | Malignant Peripheral Nerve Sheath Tumor | Reflex Epilepsy | Bruck Syndrome | MIRAGE Syndrome | REM Sleep Behavior Disorder | Megaloblastic Anemia | Rubinstein-Taybi Syndrome | Histoplasmosis | Giant Axonal Neuropathy | Primary Ovarian Insufficiency | Charcot-Marie-Tooth Disease Axonal Type 2N | Hypertension, Pulmonary | Trichomegaly | Trimethylaminuria | Charcot-Marie-Tooth Disease, Type 2 | Sepiapterin Reductase Deficiency | Atelosteogenesis Type 2 | Hypermetropia | Neurodegeneration With Brain Iron Accumulation | Warsaw Breakage Syndrome | Antiphospholipid Syndrome | Peripheral T-cell Lymphoma | Parkinson's Disease | Hyperammonemia | Hypersensitivity Pneumonitis | Leri-Weill Dyschondrosteosis | Lichen Sclerosus | Leukemia-lymphoma, Adult T-cell | Diabetic Neuropathy | Usher Syndrome Type III | Sclerosing Cholangitis | Microvillus Inclusion Disease | Oligospermia | Wiskott-Aldrich Syndrome | Waardenburg Syndrome Type 2E | Hennekam Lymphangiectasia-lymphedema Syndrome | Epidermodysplasia Verruciformis | Kohlschutter-Tonz Syndrome | Holoprosencephaly | Sensory Neuropathy | Angioedema | Sickle Cell Disease | Castleman Disease | Hereditary Multiple Exostoses | Hoyeraal-Hreidarsson Syndrome | Cerebellar Ataxia, Cayman Type | Cardiomyopathy, Dilated, 1L | Hypercalcemia | Paraganglioma, Carotid Body | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Communication Disorders | Restrictive Dermopathy | Dystrophy, Cone-rod | Schnitzler Syndrome | Kawasaki Disease | Methemoglobinemia | Neonatal Progeroid Syndrome | Neuroectodermal Tumors, Primitive | Otopalatodigital Syndrome Type 2 | Cutaneous Lupus Erythematosus | Hernia, Inguinal | Diffuse Palmoplantar Keratoderma | Spinocerebellar Ataxia Type 27 | Pseudo-pseudohypoparathyroidism | Temporal Lobe Epilepsy | Takayasu's Arteritis | Nephrotic Syndrome Type 1 | Angioimmunoblastic T-cell Lymphoma | Agoraphobia | Sclerocornea | Hypotonia-cystinuria Syndrome | Usher Syndrome Type II | Chronic Granulomatous Disease | Phosphoglycerate Dehydrogenase Deficiency | Hypercalciuria | Currarino Syndrome | Craniometaphyseal Dysplasia | Retinoblastoma | Dengue Shock Syndrome | Benign Familial Pemphigus | Twin-to-twin Transfusion Syndrome | Myofibrillar Myopathy | LEOPARD Syndrome | Pulmonary Capillary Hemangiomatosis | Carbohydrate Metabolism Disorders | Coloboma | Infectious Diarrhea | Sarcoma, Endometrial Stromal | Hermansky-Pudlak Syndrome | Hemochromatosis Type 1 | GLUT1 Deficiency Syndrome | Corneal Neovascularization | Myelofibrosis | Protein S Deficiency | Cardiomyopathy, Hypertrophic | Thin Basement Membrane Disease | Acute Myeloid Leukemia | Myasthenia Gravis | Urolithiasis | Endometriosis | Arteriovenous Malformations | Fundus Albipunctatus | Ocular Surface Squamous Neoplasia | Congenital Dyserythropoietic Anemia Type 1 | Stromal Corneal Dystrophy | Disseminated Intravascular Coagulation | Dementia | Discoid Lupus Erythematosus | Muckle-Wells Syndrome | Pearson Syndrome | Metanephric Adenoma | Pontocerebellar Hypoplasia | B-cell Prolymphocytic Leukemia | Mucolipidosis Type IV | Joubert Syndrome | Graft-versus-host Disease | Lactose Intolerance | Neurofibromatosis Type 1 | Neurocysticercosis | Pseudohypoparathyroidism Type 2 | Hypersomnia | Micro Syndrome | Hypereosinophilic Syndrome | Hypertriglyceridemia | Juvenile Polyposis | Pancytopenia | Corticobasal Syndrome | Angiodysplasia | Osteosarcoma | Hepatitis | Sezary Syndrome | Menetrier Disease | Synpolydactyly | Porokeratosis | Psoriasis | Adenoma, Pleomorphic | Steel Syndrome | Kaposiform Hemangioendothelioma | Achromatopsia | Familial Retinal Arterial Macroaneurysm | Phenylketonuria II | Farber Disease | Headache | Lissencephaly 2 | Cerebrotendinous Xanthomatosis | Swine Influenza | Eccrine Porocarcinoma | Waldenstrom Macroglobulinemia | Gyrate Atrophy Of The Choroid And Retina | Nijmegen Breakage Syndrome | Hyperinsulinemic Hypoglycemia | Polycystic Liver | Congenital Generalized Lipodystrophy | Bare Lymphocyte Syndrome | Campomelic Dysplasia | Localized Scleroderma | Necrobiosis Lipoidica | Apparent Mineralocorticoid Excess Syndrome | Congenital Disorders Of Glycosylation Type II | DICER1 Syndrome | Haim-Munk Syndrome | Mitochondrial Disease | Multicystic Renal Dysplasia | Charcot-Marie-Tooth Disease, Type 6 | Tardive Dyskinesia | Congenital Bile Acid Synthesis Defect | Chronic Beryllium Disease | Uremic Pruritus | Incontinentia Pigmenti | Lesch-Nyhan Syndrome | Familial Hypobetalipoproteinemia | Hemolytic Anemia | Acute Leukemia | Urticaria | Metabolic Diseases | Hemangioblastoma | X-linked Myotubular Myopathy | Epilepsy | Anti-glomerular Basement Membrane Disease | Primrose Syndrome | Hyperkalemic Periodic Paralysis | Periodontitis | Ulcerative Colitis | Synovitis | Generalized Epilepsy And Paroxysmal Dyskinesia | Meckel-Gruber Syndrome | Sleep Apnea, Obstructive | Frontometaphyseal Dysplasia | Pyruvate Decarboxylase Deficiency | Infertility | Smoldering Myeloma | T-cell Lymphoma, Subcutaneous Panniculitis-like | Macrodactyly | Acute Lung Injury | Polymicrogyria | Chronic Inflammatory Demyelinating Polyneuropathy | Primary Hyperoxaluria Type 3 | Osteogenesis Imperfecta Type V | Spinal Muscular Atrophy | Zellweger Syndrome | Hypertrophy | Epilepsy Of Infancy With Migrating Focal Seizures | Parvovirus B19 Infection | Hepatitis D | Urea Cycle Disorder | Primary Torsion Dystonia | Toxoplasmosis | Kallmann Syndrome