Esophagitis

About the Disease
Esophagitis, also known as acute esophagitis, is related to peptic esophagitis and esophageal candidiasis, and has symptoms including pain in esophagus (finding) An important gene associated with Esophagitis is CCL26 (C-C Motif Chemokine Ligand 26), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Acetylsalicylic acid and Trimebutine have been mentioned in the context of this disorder. Affiliated tissues include smooth muscle, lung and spinal cord, and related phenotypes are homeostasis/metabolism and immune system

Common Targets
SMO | CYSLTR1 | G7124 | FEN1 | SIGLEC5 | HRH2 | PTPRCAP | G4851 | DROSHA | FZD4 | OGG1 | GEMIN4 | FGF5 | ATP6V1C1 | E2F2 | RPS6KB2 | SMAD7 | PLCE1 | C7orf50 | DCTN5 | IL5 | Gastric H+/K+-ATPase | G3569 | IL13 | TLCD3A | ABCC3 | GPER1 | ATPase (nonspecified subtype) | G6647 | Superoxide dismutase (SOD) (nonspecified subtype) | AURKA | OR5K2 | TGFB1

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

Other Diseases

Episodic Ataxia | Lymphoma, B-cell | Glioblastoma Multiforme | Mitochondrial Encephalomyopathy | Androgenic Alopecia | Cockayne Syndrome | Pre-eclampsia | Fibromuscular Dysplasia | Kindler Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Treacher Collins Syndrome | Ocular Albinism Type 1 | Lassa Fever | Interstitial Lung Diseases | Acute Lymphocytic Leukemia | Cocaine-Related Disorders | Influenza | Autosomal Recessive Congenital Ichthyosis | Sarcoidosis | Ischemia | Papilledema | Congenital Poikiloderma | Waardenburg Syndrome Type 4A | Basan Syndrome | Turner's Syndrome | Endometritis | Poikiloderma With Neutropenia | Huntington's Disease-like 2 | Congenital Hereditary Endothelial Dystrophy Type II | Bethlem Myopathy | Wiskott-Aldrich Syndrome | Panic Disorder | Huntington's Disease | Parkinson Disease 6, Autosomal Recessive Early-onset | Fibrillation, Atrial | Multiple Sclerosis, Chronic Progressive | GAPO Syndrome | Diffuse Palmoplantar Keratoderma | Nestor-Guillermo Progeria Syndrome | Familial Glucocorticoid Deficiency | Congenital Afibrinogenemia | Heimler Syndrome | Follicular Dendritic Cell Sarcoma | Oculodentodigital Dysplasia | Astigmatism | Nephropathy | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Wolfram Syndrome 2 | Epidermolysis Bullosa Simplex, Generalized | Guttate Psoriasis | Ganglioneuroma | Tyrosinemia | Nutrition Disorders | Steel Syndrome | Personality Disorders | Hydrocephalus | Prader-Willi Syndrome | Polymyalgia Rheumatica | Panuveitis | Diastrophic Dysplasia | Persistent Hyperplastic Primary Vitreous | Cold-induced Sweating Syndrome | Endophthalmitis | Roberts Syndrome | Leishmaniasis, Visceral | Prolidase Deficiency | Feingold Syndrome | Conjunctivitis, Allergic | Conduct Disorder | Oculocutaneous Albinism | Papilloma | Atelosteogenesis Type 1 | Down Syndrome | Autoimmune Hemolytic Anemia | Chanarin-Dorfman Syndrome | Ectodermal Dysplasia | Early Infantile Epileptic Encephalopathy 28 | Posterior Polar Cataract | Tracheal Disorders | T-cell Leukemia | Familial Isolated Hyperparathyroidism | Non-Hodgkin Lymphoma | 3C Syndrome | Spinal And Bulbar Muscular Atrophy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Bronchiectasis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Charcot-Marie-Tooth Disease Type 2E | Odonto-onycho-dermal Dysplasia | Lymphoma, Mantle Cell | Charcot-Marie-Tooth Disease Type 4E | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Ataxia-ocular Apraxia 2 | Cryptococcal Meningitis | Hypertriglyceridemia | Hypertension, Renal | Hemangioma | Hyperhomocysteinemia | Corneal Ulcer | Non-proliferative Diabetic Retinopathy | Neuroleptic Malignant Syndrome | Spitz Nevus | Paroxysmal Nocturnal Hemoglobinuria | Neurodevelopmental Disorders | Wiedemann-Steiner Syndrome | Dwarfism | Restrictive Dermopathy | NDH Syndrome | Spinocerebellar Ataxia Type 15 | Chronic Idiopathic Myelofibrosis | Glutaric Aciduria Type 3 | Cholecystitis | Amyotrophic Lateral Sclerosis, Juvenile | Epithelial-myoepithelial Carcinoma | Generalized Epilepsy And Paroxysmal Dyskinesia | Coffin-Lowry Syndrome | Gestational Trophoblastic Disease | Reticular Dysgenesis | Gnathodiaphyseal Dysplasia | Birk-Barel Syndrome | Congenital Nystagmus | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Hyperlipidemia Type V | Primary Progressive Aphasia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Hypokalemia | Epidermolytic Palmoplantar Keratoderma | Primary Carnitine Deficiency | Sleep Disorder | Dengue Shock Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Meningioma | Anorchia | Mosaic Variegated Aneuploidy Syndrome 2 | Progressive Familial Intrahepatic Cholestasis Type 1 | Hypogonadism | Analgesia | Thrombotic Microangiopathy | Hyperekplexia | Niemann-Pick Disease, Type C | Nanophthalmos | Focal Facial Dermal Dysplasia | Nance-Horan Syndrome | Opisthorchiasis | Waardenburg Syndrome Type 1 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Macular Degeneration | Spinocerebellar Ataxia Type 21 | Majeed Syndrome | Corneal Dystrophy | Cerebellofaciodental Syndrome | Split Hand-foot Malformation | Autosomal Recessive Spastic Paraplegia Type 35 | Keratoconus | Familial Cerebral Amyloid Angiopathy | Gigantism | Vascular Cognitive Impairment | Leukocyte Adhesion Deficiency Type 1 | Pemphigus Vulgaris | Lichen Sclerosus | Gastritis | Angiosarcoma | Astrocytoma | Anemia | Tetraplegia | Gliosarcoma | Raine Syndrome | Autoimmune Autonomic Ganglionopathy | Anorectal Fistula | Cold Agglutinin Disease | Peritonitis | Craniopharyngioma | Pneumonia, Bacterial | Silver-Russell Syndrome | Amblyopia | Transient Bullous Dermolysis Of The Newborn | Schwannomatosis | Paracoccidioidomycosis | AIDS Dementia Complex | Pendred Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Spondyloarthritis | Pulmonary Alveolar Proteinosis | Sertoli Cell-only Syndrome | Retinopathy Of Prematurity | Nephronophthisis | Nail-Patella Syndrome | Leukemia | Avellino Corneal Dystrophy | Osteochondroma | D-2-Hydroxyglutaric Aciduria | Bullous Pemphigoid | Polymicrogyria | Brachial Plexus Neuropathy | Progressive Myoclonic Epilepsy | Retinopathy, Diabetic | Congenital Lipoid Adrenal Hyperplasia | Chediak-Higashi Syndrome | Nephroblastoma | Benign Familial Infantile Seizures | Osteoporosis | Multiple Epiphyseal Dysplasia | Osteopathia Striata With Cranial Sclerosis | Acute Tubular Necrosis | Myelitis | Leukocyte Adhesion Deficiency | Thyroid Dyshormonogenesis | Facioscapulohumeral Muscular Dystrophy | Autosomal Recessive Spastic Paraplegia Type 54 | Spinocerebellar Ataxia Type 38 | HIBCH Deficiency | Heroin Dependence | Charcot-Marie-Tooth Disease, Type 2 | CHOPS Syndrome | Osteogenesis Imperfecta Type V | Melnick-Needles Syndrome | Goiter | Delayed Sleep Phase Syndrome | DNA Ligase IV Deficiency | Glycogen Storage Disease Type 9 | Pseudoachondroplasia | Lateral Meningocele Syndrome | Cousin Syndrome | Perivascular Epithelioid Cell Tumor | Diabetes Mellitus, Transient Neonatal | Hereditary Hemorrhagic Telangiectasia | Neurocutaneous Melanocytosis | Glaucoma, Congenital | Zimmermann-Laband Syndrome | Intermittent Claudication | Fanconi Syndrome | Proopiomelanocortin Deficiency | Dystonia Musculorum Deformans | HANAC Syndrome | Arthrogryposis | Spondylosis | Optic Neuritis | Infantile Nephropathic Cystinosis | Hypoproteinemia, Hypercatabolic | Holt-Oram Syndrome | Rhabdomyosarcoma | Myasthenia Gravis | Diabetes | Chronic Kidney Disease | Becker Muscular Dystrophy | Cysticercosis | Common Variable Immunodeficiency | Lymphangioleiomyomatosis | Mitochondrial Myopathy | Hepatitis E | Sturge-Weber Syndrome | Infantile Refsum Disease | Necrobiosis Lipoidica | Systemic Mastocytosis | Smith-Kingsmore Syndrome | Adenosine Deaminase 2 Deficiency | Celiac Disease | Danon Disease | Pilomatrix Carcinoma | Hemangioendothelioma | Molybdenum Cofactor Deficiency | Cervicitis | Wolman Disease | Waardenburg Syndrome Type 4 | Hypopigmentation | Pityriasis Rubra Pilaris | Glomerulonephritis, Membranoproliferative | Nasodigitoacoustic Syndrome | Skin Fragility-woolly Hair Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Malaria, Cerebral | Focal Dermal Hypoplasia | Sarcoidosis, Pulmonary | IgA Deficiency | Recurrent Respiratory Papillomatosis | Neuroma | Varicocele | Kohlschutter-Tonz Syndrome | Stevens-Johnson Syndrome | Anodontia | Pontocerebellar Hypoplasia Type 2 | Gerstmann-Straussler-Scheinker Syndrome | Lissencephaly 2 | Congenital Generalized Lipodystrophy | Crigler-Najjar Syndrome | Dengue Hemorrhagic Fever | Gastroenteritis | Shwachman-Bodian-Diamond Syndrome | Central Core Disease | Basal Cell Nevus Syndrome | Granuloma Annulare | Neurotoxicity | Juvenile Myelomonocytic Leukemia | Vitiligo | Beta-Propeller Protein-associated Neurodegeneration | Acute Kidney Injury | Carcinoma, Squamous Cell | Depression | Brenner Tumor | Congenital Dyserythropoietic Anemia | X-linked Charcot-Marie-Tooth Disease | Neurogenic Bladder | Rothmund-Thomson Syndrome | Schnitzler Syndrome | Heterotopic Ossification | X-linked Acrogigantism | Plasma Cell Dyscrasia | Microcephaly | Urofacial Syndrome | Adenosine Deaminase Deficiency | Oculocutaneous Albinism Type 4 | Congenital Nephrotic Syndrome | Malnutrition | Glioblastoma | Dubin-Johnson Syndrome | Diabetes Insipidus, Nephrogenic | Peeling Skin Syndrome Type B | Otitis Externa | Thanatophoric Dysplasia Type 1 | GATA2 Deficiency | Nephrotic Syndrome Type 1 | Osteogenesis Imperfecta Type VI | Spinal Cord Diseases | Congenital Dysfibrinogenemia | Sclerosteosis | Cutaneous Lupus Erythematosus | Hemochromatosis | Haim-Munk Syndrome | Polyneuropathy | Hepatitis B, Chronic | Echinococcosis | Schizencephaly | Genee-Wiedemann Syndrome | Gyrate Atrophy Of The Choroid And Retina | Glycogen Storage Disease Type 3 | Anovulation | Seborrheic Dermatitis | Leri Pleonosteosis | Ileitis | Congenital Diaphragmatic Hernia | Cutaneous T-cell Lymphoma | Bartsocas-Papas Syndrome | Zellweger Syndrome | B-cell Chronic Lymphocytic Leukemia | Granular Corneal Dystrophy Type 1 | Oligospermia | Microphthalmia, Syndromic 7 | Chorea | Axenfeld-Rieger Syndrome | Greig Cephalopolysyndactyly Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Primary Sclerosing Cholangitis | Polydactyly | Tricho-hepato-enteric Syndrome | Cerebellar Ataxia, Cayman Type | Optic Atrophy 2 | Spinocerebellar Ataxia | Preaxial Polydactyly | Localized Scleroderma | Episodic Ataxia Type 2 | Macrophagic Myofasciitis | Acral Lentiginous Melanoma | Dentinogenesis Imperfecta | Imerslund-Grasbeck Syndrome | Graft-versus-host Disease | Primary Lateral Sclerosis | Agoraphobia | Binge Eating Disorder | Bartter Syndrome | Ghosal Syndrome | Sponastrime Dysplasia | Rickets | Primary Hyperoxaluria | Pseudo-pseudohypoparathyroidism | Hepatorenal Syndrome | Epidermolysis Bullosa Acquisita | Measles | Primary Torsion Dystonia | Empyema | Liver Diseases | Lymphangiomatosis | Cavitary Optic Disc Anomalies | Congenital Heart Block | Hypertelorism | Seminoma | Chronic Inflammatory Demyelinating Polyneuropathy | Lactose Intolerance | Behavioral Variant Of Frontotemporal Dementia | 3-M Syndrome | Rheumatic Heart Disease | Cutis Laxa | Hemangioblastoma | Antiphospholipid Syndrome | Polycythemia | Angioedema, Hereditary | Spondylocostal Dysostosis | Renpenning Syndrome | Restless Legs Syndrome | Retinal Vasculitis | Congenital Myasthenic Syndrome