Opisthorchiasis

About the Disease
Opisthorchiasis, also known as infection by opisthorchis, is related to fascioliasis and duodenal ulcer. An important gene associated with Opisthorchiasis is IL4 (Interleukin 4), and among its related pathways/superpathways are Overview of interferons-mediated signaling pathway and Bacterial infections in CF airways. Affiliated tissues include liver, pancreas and small intestine.

Common Targets
SOCS5 | PIAS3

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

Other Diseases

Carey-Fineman-Ziter Syndrome | Nephrocalcinosis | Sarcoma, Alveolar Soft Part | Stevens-Johnson Syndrome | Granular Corneal Dystrophy Type 1 | Hartnup Disease | Congenital Torticollis | Protein S Deficiency | Palmoplantar Keratoderma | Hairy Cell Leukemia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Diabetes Insipidus | Vici Syndrome | Macular Degeneration | Gangliosidosis, GM1 | Osteochondrosis | Postpartum Depression | Keratosis | X-linked Creatine Transporter Deficiency | Cenani-Lenz Syndactyly Syndrome | Strabismus | Hereditary Neuropathy With Liability To Pressure Palsies | Conjunctivitis | Chronic Granulomatous Disease | Molybdenum Cofactor Deficiency | Desbuquois Syndrome | Vascular Calcification | Lymphopenia | Carpal Tunnel Syndrome | Diabetic Encephalopathy | Cardiomyopathy, Dilated, 1L | Endometriosis | Holt-Oram Syndrome | Enhanced S-cone Syndrome | Small Lymphocytic Lymphoma | Dermatitis | Hypohidrotic Ectodermal Dysplasia | Osteoporosis-pseudoglioma Syndrome | Bipolar Disorder | 5-oxoprolinase Deficiency | DOCK8 Immunodeficiency Syndrome | Branchiootorenal Syndrome | Adenoma, Villous | Meningeal Melanocytoma | Pre-eclampsia | Benign Hereditary Chorea | Gastritis | Leukemia | Epidermolysis Bullosa Simplex, Generalized | Alzheimer Disease, Late Onset | Blepharitis | Richter's Syndrome | Lamellar Ichthyosis | Acute Coronary Syndrome | Basal Ganglia Disease, Biotin-responsive | Donnai-Barrow Syndrome | Rolandic Epilepsy | Multiple Sclerosis, Primary Progressive | Pyoderma Gangrenosum | Congenital Poikiloderma | Cerebrotendinous Xanthomatosis | Dentinogenesis Imperfecta | Cutaneous Mastocytosis | Communication Disorders | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Auriculocondylar Syndrome | Marshall-Smith Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Gastric Atrophy | Astrocytoma, Anaplastic | Axenfeld-Rieger Syndrome | Hereditary Sensory And Autonomic Neuropathy | Fibrillation, Atrial | Malignant Peripheral Nerve Sheath Tumor | Aneurysm, Abdominal Aortic | Episodic Ataxia Type 2 | Pleomorphic Xanthoastrocytoma | Asperger Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Feingold Syndrome | Diabetic Neuropathy | Hyperacusis | Anorectal Fistula | Infertility, Male | Focal Cortical Dysplasia Type 2 | Primary Progressive Nonfluent Aphasia | Sturge-Weber Syndrome | Xeroderma Pigmentosum Variant Type | Asthma, Exercise-induced | Porokeratosis | Fukuyama Congenital Muscular Dystrophy | Retinitis Pigmentosa 3 | Trichuriasis | Relapsing Polychondritis | Glutaric Aciduria Type 2 | Alpers Syndrome | Alopecia | Diabetes Type 2 | Familial Advanced Sleep Phase Syndrome | Periventricular Leukomalacia | Antisocial Personality Disorder | Osteogenesis Imperfecta Type VI | Asthma | Withdrawal Syndrome | Acromicric Dysplasia | Neurocysticercosis | Stiff-man Syndrome | Nemaline Myopathy 10 | Charcot-Marie-Tooth Disease, Type 1A | Hypotrichosis Simplex | Chromosome 17q21.31 Deletion Syndrome | Congenital Nystagmus | Primary Sclerosing Cholangitis | Colon Adenoma | Menkes Disease | Sjogren Syndrome | Diabetes | Neutrophilia | Ophthalmoplegia | Hereditary Mixed Polyposis Syndrome | Cabezas Syndrome | Retinoblastoma | Sporadic Hemiplegic Migraine | Riboflavin Transporter Deficiency Neuronopathy | Graft-versus-host Disease | Angioedema | Limb Girdle Muscular Dystrophy | Hypersomnia | Cataract | Thrombophilia | Castleman Disease | Familial Hemiplegic Migraine | Carcinoid Syndrome | Ichthyosis Bullosa Of Siemens | Vitamin B12 Deficiency | Eclampsia | Adenoid Cystic Carcinoma | Liver Diseases | Zygomycosis | D-2-Hydroxyglutaric Aciduria | Inflammatory Bowel Disease | Bronchitis | Keratitis-ichthyosis-deafness Syndrome | Osteogenesis Imperfecta Type III | Tetanus | Aarskog-Scott Syndrome | Goiter, Nodular | Uveitis | Cryptosporidiosis | Analgesia | Guanidinoacetate Methyltransferase Deficiency | Nasodigitoacoustic Syndrome | Tendinopathy | Spinocerebellar Ataxia Type 17 | Hereditary Multiple Exostoses | Carcinoma, Signet Ring Cell | Bartter Syndrome | Tatton-Brown-Rahman Syndrome | Charcot-Marie-Tooth Disease Type 4E | Episodic Ataxia Type 1 | Congenital Myopathy | Schuurs-Hoeijmakers Syndrome | Hamartoma | Persistent Hyperplastic Primary Vitreous | Leukodystrophies | Turner's Syndrome | Cardiac Arrest | Pathological Gambling | Desmosterolosis | Christianson Syndrome | Spondylosis | Duodenal Atresia | Dysequilibrium Syndrome | X-linked Charcot-Marie-Tooth Disease | Schindler Disease | Wagner Disease | Nephrosclerosis | Infantile Liver Failure Syndrome 1 | Bulimia Nervosa | Osteogenesis Imperfecta Type I | Leukocyte Adhesion Deficiency Type 1 | Hemangioma | Acute Generalized Exanthematous Pustulosis | Ganglioneuroma | Cysticercosis | Pneumoconiosis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Hemoglobinopathies | Diabetes Type 1 | Cornelia De Lange Syndrome | Plasma Cell Leukemia | Acral Lentiginous Melanoma | Vestibular Disease | Retinal Dystrophy | Osmotic Demyelination Syndrome | Roberts Syndrome | Hypobetalipoproteinemias | Fuchs Heterochromic Iridocyclitis | Greig Cephalopolysyndactyly Syndrome | Peeling Skin Syndrome, Acral Type | Fowler's Syndrome | Prolidase Deficiency | Astrocytoma | Malignant Fibrous Histiocytoma | Stroke, Hemorrhagic | Autonomic Nervous System Disorders | Nail-Patella Syndrome | Cherubism | Triple A Syndrome | Myelitis | Emery-Dreifuss Muscular Dystrophy | Charcot-Marie-Tooth Disease, Type 6 | Seborrheic Dermatitis | Sialidosis Type I | 3C Syndrome | Adult Polyglucosan Body Disease | Central Retinal Artery Occlusion | Exotropia | Warsaw Breakage Syndrome | Rubinstein-Taybi Syndrome | HUPRA Syndrome | Meningioma, Benign | VACTERL Association | Infantile Nephropathic Cystinosis | Infantile Neuroaxonal Dystrophy | Prune Belly Syndrome | Patent Foramen Ovale | Nemaline Myopathy | Vitelliform Macular Dystrophy | Hypertensive Retinopathy | Diffuse Palmoplantar Keratoderma | Lassa Fever | Systemic Mastocytosis | Carcinoma, Transitional Cell | Gingivitis | Primary Familial Brain Calcification | Schizoaffective Disorder | Oligoasthenoteratozoospermia | Myelomeningocele | Congenital Muscular Dystrophy | Hypermethioninemia | Primrose Syndrome | Esophageal Carcinoma | Blood Protein Disorders | Corticobasal Syndrome | Juvenile Polyposis | Hepatitis E | Schizophrenia, Paranoid | Mitochondrial Cytopathy | CREST Syndrome | Epidermolysis Bullosa Simplex | Nestor-Guillermo Progeria Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Precocious Puberty | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Seizures | Congenital Hereditary Endothelial Dystrophy Type I | Leber Congenital Amaurosis | Exocrine Pancreatic Insufficiency | Apparent Mineralocorticoid Excess Syndrome | Pachyonychia Congenita | Pyruvate Carboxylase Deficiency Disease | Acne Vulgaris | Melanoma, Uveal | Batten Disease | Eiken Syndrome | Renal Failure | Discoid Lupus Erythematosus | Methemoglobinemia Type IV | Myelitis, Transverse | Cramp Fasciculation Syndrome | Cryopyrin-associated Periodic Syndromes | Mucolipidosis Type II | Seminoma | Waardenburg Syndrome Type 1 | Sickle Cell Anemia | Basal Cell Nevus Syndrome | Pituitary Disorders | Malaria, Cerebral | Spondyloepiphyseal Dysplasia Tarda, X-linked | KBG Syndrome | Pantothenate Kinase-associated Neurodegeneration | Calcium Pyrophosphate Deposition Disease | FG Syndrome | Colorectal Adenoma | Giant Cell Glioblastoma | DiGeorge Syndrome | Veno-occlusive Disease | Craniopharyngioma | Benign Familial Neonatal Convulsions | CHOPS Syndrome | Otitis Externa | Intracranial Hypertension | Impetigo | Nail Disorder, Nonsyndromic Congenital | Chronic Thromboembolic Pulmonary Hypertension | Spinocerebellar Ataxia Type 3 | Loeys-Dietz Syndrome Type 4 | Prolactinoma | Carotid Artery Disease | Hypocalcemia | Gitelman Syndrome | Cellulitis | Membranous Nephropathy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Periodontitis | Dystonia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Ulcerative Colitis | Chordoid Glioma | Thyrotoxic Periodic Paralysis | Tardive Dyskinesia | Pontocerebellar Hypoplasia Type 7 | Neurofibromatosis | Encephalitis | Spinocerebellar Ataxia Type 16 | Toxic Epidermal Necrolysis | VACTERL/VATER Association | Juvenile Hyaline Fibromatosis | Postaxial Polydactyly | Allan-Herndon-Dudley Syndrome | Steel Syndrome | Arthritis, Psoriatic | Fibromyalgia | Phosphoglycerate Dehydrogenase Deficiency | Nanophthalmos | Hashimoto Thyroiditis | Pleurisy | Glioblastoma | Intestinal Tuberculosis | Anal Fissure | Swine Influenza | Stickler Syndrome | Plasma Cell Dyscrasia | WAGR Syndrome | Menetrier Disease | Metanephric Adenoma | Gardner Syndrome | Hypoparathyroidism | PHARC Syndrome | Urofacial Syndrome | Heterotopic Ossification | Endocarditis | Usher Syndrome Type IIC | Scleroderma, Diffuse | Rhabdomyosarcoma, Alveolar | Allergic Contact Dermatitis | Myeloid Leukemia | Cholangitis | Chorea-acanthocytosis | Hyperferritinemia-cataract Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Li-Fraumeni Syndrome | Hyperparathyroidism | Mucolipidosis Type IV | Neuroblastoma | Blepharospasm | Charcot-Marie-Tooth Disease Type 4 | Kohlschutter-Tonz Syndrome | Wiedemann-Steiner Syndrome | Peroxisomal Disorder | Johanson-Blizzard Syndrome | Agoraphobia | Smith-Lemli-Opitz Syndrome | Liddle Syndrome | GNE Myopathy | Osteosarcoma | Hydrops Fetalis | Rett Syndrome | Congenital Sodium Diarrhea | Wolfram Syndrome 2 | Lymphoma, Mantle Cell | SAPHO Syndrome | Corneal Dystrophy And Perceptive Deafness | Inflammatory Joint Disease | Glaucomatocyclitic Crisis | Coronary Restenosis | Carcinoid Tumor | Restrictive Dermopathy | Anthrax | Down Syndrome | Vitamin D Deficiency | Pierre Robin Syndrome | Bloom Syndrome | Polycythemia | Multicentric Carpotarsal Osteolysis Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Chronic Inflammatory Demyelinating Polyneuropathy | Familial Partial Lipodystrophy | Spondylolisthesis | Woodhouse-Sakati Syndrome | Omenn Syndrome | Tumoral Calcinosis | Vertebrobasilar Insufficiency | Diastrophic Dysplasia | Usher Syndrome Type II | Pituitary Dwarfism | Deafness, Dystonia, And Cerebral Hypomyelination | Follicular Dendritic Cell Sarcoma