Hepatitis

About the Disease
Hepatitis, also known as chronic persistent hepatitis, is related to hepatitis c and hepatitis a, and has symptoms including abdominal pain, constipation and diarrhea. An important gene associated with Hepatitis is HAVCR1 (Hepatitis A Virus Cellular Receptor 1), and among its related pathways/superpathways are Toll-like receptor signaling pathway and Ebola virus infection in host. The drugs Glycyrrhizic acid and Acarbose have been mentioned in the context of this disorder. Affiliated tissues include liver, kidney and t cells, and related phenotypes are no effect and no effect

Common Targets
G5599 | G7099 | CD3 Complex (T Cell Receptor Complex) | MSH3 | PDE4B | Ribonucleoside-diphosphate reductase | DGAT1 | HLA-B | G4780 | SPHK2 | NAT2 | Thyroid hormone receptor (nonspecified subtype) | IFI44L | BRD4 | MAP3K5 | G2475 | KEAP1 | PDE10A | G7124 | HLA-A | CYP2E1 | PGAM5-KEAP1-NRF2 Complex | APOC3 | GSTT1 | NEK7 | G581 | TLR2 | G836 | UGT1A6 | G5743 | G4233 | QPCT | Caspase (nonspecified subtype) | PDE1B | IL10 | PDE2A | STK4 | TLR9 | NOS2 | CCL20 | GSTM1 | SLCO1B1 | RAB5A | IL1B | UGT1A1 | IFNL4 | G3146 | G3569 | DHFR | ABCB11 | KRR1 | HSPA1L | GSPT1 | TNFRSF1A | TBK1 | RIPK1 | LY96 | NF-kappaB (NFkB) | TLR4/MD-2 complex | G6774 | G5133 | PDE3A | PDE7A | DNA-Directed DNA Polymerase Complex | CARD8 | IL12B | EDNRA | SPP1 | CD209 | G29126

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Other Diseases

Retinopathy Of Prematurity | Occipital Neuralgia | Acute Coronary Syndrome | Hepatitis, Alcoholic | Hernia, Inguinal | Dysferlinopathy | Pulmonary Capillary Hemangiomatosis | Spinocerebellar Ataxia Type 15 | Ataxia-ocular Apraxia 2 | Pseudohypoparathyroidism Type 1C | X-linked Creatine Transporter Deficiency | Protein S Deficiency | Hypertensive Nephropathy | Martsolf Syndrome | Gnathodiaphyseal Dysplasia | Oculocutaneous Albinism Type 2 | Hypohidrotic Ectodermal Dysplasia, X-linked | Poirier-Bienvenu Neurodevelopmental Syndrome | Dwarfism | Synovitis | Spinal Muscular Atrophy Type 3 | Autosomal Recessive Bestrophinopathy | Prurigo Nodularis | Neurofibromatosis | Chronic Periodontitis | Spondylometaphyseal Dysplasia | Tyrosinemia Type 2 | Hemolytic Uremic Syndrome, Atypical | Antenatal Bartter Syndrome Type 1 | Fahr Disease | Omenn Syndrome | Keratocystic Odontogenic Tumor | Keratoacanthoma | Chronic Thromboembolic Pulmonary Hypertension | Prune Belly Syndrome | Enterocolitis, Necrotizing | Encephalopathy, Glycine | Renpenning Syndrome | Neuropathy | Snyder-Robinson Syndrome | Early Infantile Epileptic Encephalopathy 4 | Iron Deficiency Anemia | Schizophrenia, Paranoid | Raynaud Phenomenon | Leprosy | Chronic Neutrophilic Leukemia | Stargardt Disease | Acute Lung Injury | Ischemia | Stroke, Hemorrhagic | Diamond-Blackfan Anemia | Mohr-Tranebjaerg Syndrome | Spinocerebellar Ataxia Type 38 | Chondrodysplasia Punctata 2, X-linked Dominant | Chitayat Syndrome | Mitochondrial Disease | VACTERL/VATER Association | Galactosemia | Nemaline Myopathy 10 | Chloridorrhea, Congenital | Spinocerebellar Ataxia Type 12 | Hypereosinophilic Syndrome | Hypotonia-cystinuria Syndrome | Cutaneous T-cell Lymphoma | Keloid | Pemphigus Foliaceus | Reticular Dysgenesis | Sturge-Weber Syndrome | Wolfram Syndrome 2 | Esophagitis | Myofibromatosis | Retinopathy, Diabetic | Anorexia Nervosa | Tremor | Specific Granule Deficiency | Glanzmann Thrombasthenia | Lipodystrophy | Gastritis, Atrophic | Non-proliferative Diabetic Retinopathy | Alzheimer Disease, Late Onset | Membranous Nephropathy | Motor Neuron Diseases | Bicuspid Aortic Valve | Impetigo | Alexander Disease | Familial Advanced Sleep Phase Syndrome | Carpal Tunnel Syndrome | Charcot-Marie-Tooth Disease Type 3 | Congenital Fiber-type Disproportion Myopathy | Cystinosis | Hypoplastic Left Heart Syndrome | Peripheral T-cell Lymphoma | Hypercholesterolemia | Apraxia | Purpura | Anthrax | Osteogenesis Imperfecta | Peyronie's Disease | Endophthalmitis | Hepatitis D | Encephalitis, Tick-borne | Chorea | Familial Partial Lipodystrophy | Loeys-Dietz Syndrome Type 4 | Hyperkalemic Periodic Paralysis | Gastroschisis | Progressive Familial Intrahepatic Cholestasis | Hypoalbuminemia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Zollinger-Ellison Syndrome | Fanconi Anemia | Optic Nerve Hypoplasia, Bilateral | Primary Erythromelalgia | Bardet-Biedl Syndrome | Werner's Syndrome | Fragile X Syndrome | B-cell Chronic Lymphocytic Leukemia | Glycogen Storage Disease Type 4 | Methylmalonic Acidemia | Acne | Parkinson Disease 6, Autosomal Recessive Early-onset | Multiple Sulfatase Deficiency | Cyclic Vomiting Syndrome | Spinal And Bulbar Muscular Atrophy | Niemann-Pick Disease, Type B | 3-methylglutaconic Aciduria Type I | Tuberculous Meningitis | Mesothelioma, Malignant | Autosomal Recessive Spastic Paraplegia Type 75 | IMAGe Syndrome | Peripheral Neuropathy | Cockayne Syndrome | Onchocerciasis | Peroxisomal Disorder | Osteonecrosis | Mitochondrial DNA Depletion Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Esophageal Adenocarcinoma | Palsy, Cerebral | Neurofibromatosis-Noonan Syndrome | Obsessive-compulsive Disorder | Congenital Primary Aphakia | Sporadic Inclusion Body Myositis | Adrenomyeloneuropathy | Ocular Albinism Type 1 | Chondrosarcoma | Charcot-Marie-Tooth Disease, Type 2 | Aldosteronism | Bronchiolitis | Hydrops Fetalis | Oculopharyngeal Muscular Dystrophy | Adenomyosis | Aneurysm, Abdominal Aortic | Sarcoma | 3-methylglutaconic Aciduria | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Chromosome 16p11.2 Deletion Syndrome | LRBA Deficiency | Polycystic Kidney, Autosomal Dominant | Angiosarcoma Of The Breast | Infantile Nephropathic Cystinosis | Oculodentodigital Dysplasia | Oligospermia | Hemangioendothelioma | Tinea | Glycogen Storage Disease Type 1b | Christianson Syndrome | Dementia | Sengers Syndrome | Retinoschisis | Hereditary Mixed Polyposis Syndrome | Diabetes Insipidus, Nephrogenic | Adams-Oliver Syndrome | Schwannomatosis | Chiari Malformation Type I | Spinocerebellar Ataxia Type 7 | Parkinsonism | Ornithine Transcarbamylase Deficiency | Hydrolethalus Syndrome | Scleroderma | Vulvovaginitis | Thromboembolism | Encephalocele | Headache | Stroke, Ischemic | Tracheal Disorders | Disseminated Intravascular Coagulation | Delirium | Meier-Gorlin Syndrome | Hemochromatosis Type 1 | Erectile Dysfunction | Hartsfield Syndrome | Hypersensitivity Pneumonitis | Leber Congenital Amaurosis | Walker-Warburg Syndrome | Kidney Stones | Neuroma | Hyperostosis | Congenital Muscular Dystrophy | Cerebellofaciodental Syndrome | Sotos Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Graves Disease | Pseudomyxoma Peritonei | Charcot-Marie-Tooth Disease Type 2T | Microcephalic Primordial Dwarfism | Periventricular Leukomalacia | Neurotoxicity | Loeys-Dietz Syndrome | Epithelioid Hemangioma | Roberts Syndrome | Hyperacusis | Hepatitis B, Chronic | Epidermal Nevus Syndrome | Rash | Herpes Genitalis | Acrodermatitis Enteropathica | Retinal Telangiectasia | Papulopustular Rosacea | Osteogenesis Imperfecta Type I | Chordoid Glioma | Ocular Surface Squamous Neoplasia | Myoclonic Atonic Epilepsy | Erythromelalgia | Rhizomelic Chondrodysplasia Punctata | Acanthosis Nigricans | Strabismus | Photosensitivity | Acute Generalized Exanthematous Pustulosis | Alopecia | Spitzoid Melanoma | Blomstrand Osteochondrodysplasia | Cabezas Syndrome | Neovascular Glaucoma | T-cell Prolymphocytic Leukemia | Greenberg Dysplasia | Presbycusis | Goiter | Arteriosclerosis | Amelanotic Melanoma | GLUT1 Deficiency Syndrome | Glomerulonephritis | Anencephaly | Glomerulonephritis, Membranous | Neuroleptic Malignant Syndrome | Stevens-Johnson Syndrome | 3-methylglutaconic Aciduria Type IV | 3-methylcrotonyl-CoA Carboxylase Deficiency | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hypodontia | Pontocerebellar Hypoplasia Type 2 | Gigantism | Pituitary Disorders | Whipple's Disease | Dermatofibrosarcoma | Hemangioma | Hyperprolactinemia | Xeroderma Pigmentosum | Granuloma Annulare | Pseudoachondroplasia | Perivascular Epithelioid Cell Tumor | Intellectual Disability, Autosomal Dominant 5 | Gardner Syndrome | Early Infantile Epileptic Encephalopathy 13 | Periodic Limb Movement Disorder | Dysthymia | Familial Episodic Pain Syndrome | Cancer, Brain | Ureteropelvic Junction Obstruction | Waardenburg Syndrome Type 2 | Cholera | Cirrhosis | Congenital Bilateral Absence Of Vas Deferens | Retinal Dystrophy | Sleep Apnea | Actinomycetoma | Subcortical Band Heterotopia | Pierson Syndrome | Congenital Adrenal Hyperplasia 1 | Lymphoproliferative Disease, X-linked | Cardiac Sarcoidosis | Alpers Syndrome | Axenfeld-Rieger Syndrome | Panuveitis | Budd-Chiari Syndrome | Pemphigus | Tetanus | Adenoma, Villous | Arthropathy | Hermansky-Pudlak Syndrome | Hypotrichosis Simplex | Schindler Disease | Temtamy Preaxial Brachydactyly Syndrome | Pneumonia, Bacterial | Infertility, Male | Gaucher Disease | Hyperthyroidism | Pancreatitis, Chronic | Follicular Dendritic Cell Sarcoma | Depression | Multiple Myeloma | Sleep Apnea, Obstructive | Spondyloepiphyseal Dysplasia Tarda, X-linked | Pearson Syndrome | Pseudohypoaldosteronism | Lennox-Gastaut Syndrome | Sitosterolemia | Achromatopsia | Rosacea | Alpha-1 Antitrypsin Deficiency | Impulse Control Disorder | Nemaline Myopathy | Raine Syndrome | Central Pain Syndrome | Pseudohermaphroditism | Phenylketonuria II | Lymphoma, AIDS-related | Glutaric Aciduria Type 2 | Charcot-Marie-Tooth Disease, Type 1A | Hemosiderosis | Lymphoproliferative Disorders | Constipation | Porphyria | Ileitis | B-cell Prolymphocytic Leukemia | Renal Tubular Acidosis | Barakat Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Anorchia | Lymphoma, Mantle Cell | Infantile Neuroaxonal Dystrophy | Atrial Septal Defect | Gastrointestinal Disorders | Nasodigitoacoustic Syndrome | Epidermolysis Bullosa Simplex | Dyggve-Melchior-Clausen Disease | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Urolithiasis | Ebstein Anomaly | X-linked Sideroblastic Anemia | Epidermodysplasia Verruciformis | Non-epidermolytic Palmoplantar Keratoderma | Tetraplegia | Uveitis | Otopalatodigital Syndrome Type 2 | Allan-Herndon-Dudley Syndrome | T-cell Chronic Lymphocytic Leukemia | Hashimoto Thyroiditis | Zimmermann-Laband Syndrome | Multiple Epiphyseal Dysplasia | Oligoastrocytoma | Retinitis | Paraplegia | Glutaric Aciduria Type 3 | Hemochromatosis | Greig Cephalopolysyndactyly Syndrome | Dowling-Degos Disease | Chondromyxoid Fibroma | Vertebrobasilar Insufficiency | Currarino Syndrome | 3-M Syndrome | Microphthalmia | Schizophrenia | Desbuquois Syndrome | Pneumoconiosis | Agammaglobulinemia | Multisystemic Smooth Muscle Dysfunction Syndrome | Corneal Dystrophy | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Erythema Nodosum | Non-bullous Congenital Ichthyosiform Erythroderma | Kallmann Syndrome | Cenani-Lenz Syndactyly Syndrome | Ectrodactyly | Presbyopia | Primary Hyperoxaluria Type 3 | Noonan Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Urea Cycle Disorder | Glioma | Alkaptonuria | Autoimmune Polyendocrine Syndrome | Waardenburg Syndrome Type 4 | Dupuytren Disease | Precocious Puberty | Limb Girdle Muscular Dystrophy | Carcinoma, Merkel Cell | Liver Failure, Acute Infantile | Meningeal Melanocytoma | Familial Mediterranean Fever | Spinocerebellar Ataxia Type 20 | Monilethrix | Skin Carcinoma | Alstrom Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Pulmonary Stenosis | Hypokalemia | Postpartum Depression | Viral Meningitis | Majeed Syndrome