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.ai.

Other Diseases

Amelogenesis Imperfecta | Lymphangiomatosis | Palsy, Cerebral | Centronuclear Myopathy | Sertoli Cell-only Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Exocrine Pancreatic Insufficiency | Neurofibrosarcoma | Distal Myopathy | Metachromatic Leukodystrophy | Glycogen Storage Disease Type 1b | Macrodactyly | Platelet Disorders | Trichothiodystrophy | Agammaglobulinemia | Infantile Refsum Disease | Congenital Mirror Movements | Hepatic Adenomatosis | Blepharophimosis Syndrome | Hepatic Veno-occlusive Disease | Rubinstein-Taybi Syndrome | Persistent Mullerian Duct Syndrome | Choriocarcinoma | Wolfram Syndrome | Anal Fissure | Adenoid Cystic Carcinoma | Stromal Corneal Dystrophy | 3-hydroxy-3-methylglutaric Aciduria | Autonomic Neuropathy | Chronic Mucocutaneous Candidiasis | Arthritis, Gouty | Esophagitis | Whipple's Disease | Multiple Sclerosis | Rhabdomyosarcoma | Blau Syndrome | Guillain-Barre Syndrome | Gastroenteritis | Goiter, Nodular | Antisynthetase Syndrome | Hypercalciuria | Tendinopathy | Meningitis | Rheumatoid Arthritis | Asthma, Exercise-induced | Myocarditis | Leigh Syndrome | Sick Sinus Syndrome | Charcot-Marie-Tooth Disease Type 4D | Blepharo-cheilo-odontic Syndrome | Hypocalcemia | Kabuki Syndrome 2 | Herpes Simplex Dermatitis | Anti-NMDA Receptor Encephalitis | Acne | Seborrheic Dermatitis | Congenital Primary Aphakia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Mitochondrial Disease | Posterior Polar Cataract | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Juvenile Myoclonic Epilepsy | Prolymphocytic Leukemia | Epidermolysis Bullosa | Progressive Osseous Heteroplasia | Pneumothorax | Sarcoidosis, Pulmonary | Hypothalamic Obesity | Donnai-Barrow Syndrome | Marshall-Smith Syndrome | Takayasu's Arteritis | Membranous Nephropathy | Angelman Syndrome | Melanoma, Malignant | Pituitary Dwarfism | Allan-Herndon-Dudley Syndrome | Congenital Adrenal Hyperplasia | Retinopathy Of Prematurity | Infectious Diarrhea | Rash | Spinocerebellar Ataxia Type 8 | Retinoschisis | Gerstmann-Straussler-Scheinker Syndrome | HUPRA Syndrome | Infertility, Male | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Antenatal Bartter Syndrome Type 1 | Diabetes Insipidus, Nephrogenic | Parapsoriasis | Fucosidosis | Hepatitis A | Senior-Loken Syndrome | Myhre Syndrome | Familial Pheochromocytoma-paraganglioma | Pyruvate Decarboxylase Deficiency | Frontometaphyseal Dysplasia | Cyclic Vomiting Syndrome | Neurocysticercosis | Scoliosis | Retinal Coloboma | Granuloma Annulare | Pneumococcal Meningitis | Gout | Hereditary Spastic Paraplegia | Periodic Limb Movement Disorder | Sitosterolemia | Dubin-Johnson Syndrome | Raine Syndrome | Myocardial Infarction | Heroin Dependence | Lymphopenia | Weill-Marchesani Syndrome | Dystonia-parkinsonism, X-linked | Hemimegalencephaly | Spastic Paraplegia Type 7 | Kashin-Beck Disease | Neurofibromatosis Type 2 | Acrodermatitis Enteropathica | Spinocerebellar Ataxia Type 21 | Ebstein Anomaly | Congenital Disorders Of Glycosylation | Erythema Nodosum | MELAS Syndrome | Cardiomyopathy, Peripartum | Amyotrophic Lateral Sclerosis, Juvenile | Pneumonia, Viral | Subacute Sclerosing Panencephalitis | Ovarian Hyperstimulation Syndrome | Barrett Esophagus | Tinea | Pulmonary Vein Stenosis | Alpers Syndrome | Metachondromatosis | Diabetes Type 1 | Osteoporosis, Postmenopausal | Coronary Artery Disease | Greig Cephalopolysyndactyly Syndrome | Hypermethioninemia | Hypereosinophilic Syndrome | Acromesomelic Dysplasia | Lennox-Gastaut Syndrome | Meier-Gorlin Syndrome | Congenital Heart Block | Oligodendroglioma | Encephalopathy, Hepatic | Hypospadias | Chanarin-Dorfman Syndrome | Hypersomnia | Pyruvate Kinase Deficiency | Cystitis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Diverticulitis | Basal Cell Nevus Syndrome | Malignant Peripheral Nerve Sheath Tumor | Syndactyly | Pemphigus | Autosomal Recessive Congenital Ichthyosis | Kaposiform Hemangioendothelioma | Pulverulent Zonular Cataract | Central Retinal Artery Occlusion | Jaundice, Obstructive | Carney Triad | Microcephaly, Seizures, And Developmental Delay | Glucagonoma | Otosclerosis | Pupil Disorders | Palmoplantar Keratoderma | Hyperlipidemia Type V | Osteogenesis Imperfecta Type I | Familial Hyperaldosteronism | Cancer, Bladder | Polycystic Ovary Syndrome | Leishmaniasis, Cutaneous | Leri Pleonosteosis | Ichthyosis Hystrix, Curth-Macklin Type | Lymphoma, B-cell | Scleroderma | Ameloblastic Carcinoma | Asplenia | Paracoccidioidomycosis | Alopecia Totalis | Ehlers-Danlos Syndrome | Erectile Dysfunction | Creutzfeldt-Jakob Disease | Reye Syndrome | Hemorrhagic Disorders | Werner's Syndrome | Niemann-Pick Disease, Type B | Lichen Sclerosus | Leukocyte Adhesion Deficiency | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Granular Corneal Dystrophy Type 1 | 3-methylglutaconic Aciduria Type I | Paroxysmal Nocturnal Hemoglobinuria | Incontinentia Pigmenti | Pseudo-pseudohypoparathyroidism | Congenital Ichthyosiform Erythroderma | Acute Lung Injury | Methemoglobinemia | Narcolepsy | Neurotoxicity | Acral Lentiginous Melanoma | Thrombocytopenia | Spinal Muscular Atrophy Type 3 | Occipital Neuralgia | Sick Sinus Syndrome 1 | Polycythemia | Peroxisomal Disorder | Multiple Sclerosis, Chronic Progressive | Cat Eye Syndrome | Pierpont Syndrome | Myopathy | Pseudoexfoliation Syndrome | Blastoma, Pleuropulmonary | Aplasia Cutis Congenita | Chronic Granulomatous Disease, X-linked | Imerslund-Grasbeck Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Cystitis, Interstitial | Micropenis | Chronic Lymphocytic Leukemia | Glutaric Aciduria Type 2 | Retinal Dystrophy | Cranioectodermal Dysplasia | Histiocytosis | Cole-Carpenter Syndrome | Dysmorphophobia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Angioedema | Hereditary Xerocytosis | Intestinal Obstruction | Chorioretinitis | Early Infantile Epileptic Encephalopathy | Restrictive Dermopathy | Urolithiasis | Hairy Cell Leukemia | Psoriasis | Histiocytic Sarcoma | Atrioventricular Septal Defect | Spinocerebellar Ataxia Type 23 | Goiter | Long QT Syndrome Type 1 | Peters-plus Syndrome | Tremor | Gigantism | Hyperandrogenemia | Conjunctivitis, Allergic | Disseminated Intravascular Coagulation | PASLI Disease | Hyperammonemia | Johanson-Blizzard Syndrome | Conduct Disorder | Adenylosuccinate Lyase Deficiency | FG Syndrome | Rickets | Spitz Nevus | Hyperparathyroidism, Primary | Cryptococcal Meningitis | Hypoalbuminemia | Fragile X Syndrome | Spermatocele | Progressive Familial Intrahepatic Cholestasis Type 2 | Vascular Cognitive Impairment | Sarcoma | Trichuriasis | Dementia, Vascular | Personality Disorders | Acanthosis Nigricans | Hoyeraal-Hreidarsson Syndrome | Pelizaeus-Merzbacher Disease | Hyperferritinemia-cataract Syndrome | Hepatitis, Autoimmune | Polyarteritis Nodosa | Scapuloperoneal Myopathy, X-linked Dominant | Hyperbilirubinemia, Neonatal | Apraxia | SAPHO Syndrome | Myofibrillar Myopathy | Thin Basement Membrane Disease | Infantile Spasm | VACTERL Association | Spinocerebellar Ataxia | Adrenoleukodystrophy, X-linked | Otitis Externa | Silver-Russell Syndrome | Sickle Cell Disease | Epicondylitis | Hypohidrotic Ectodermal Dysplasia, X-linked | Ependymoma | Hereditary Pyropoikilocytosis | Coenzyme Q10 Deficiency | Gray Platelet Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Crigler-Najjar Syndrome | Pantothenate Kinase-associated Neurodegeneration | Ataxia-ocular Apraxia 2 | Congenital Fiber-type Disproportion Myopathy | Congenital Diaphragmatic Hernia | Menetrier Disease | Lattice Corneal Dystrophy Type 1 | Spinocerebellar Ataxia Type 12 | Non-Langerhans Cell Histiocytosis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Cardiomyopathy, Hypertrophic | Cerebrovascular Disorders | Dysequilibrium Syndrome | Measles | Trigonocephaly | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Pyoderma Gangrenosum | Hypervalinemia | Methemoglobinemia Type IV | Congenital Dyserythropoietic Anemia Type 1 | Pseudohermaphroditism | Hereditary Sensory And Autonomic Neuropathy | Bainbridge-Ropers Syndrome | Smoldering Myeloma | Encephalopathy, Ethylmalonic | Ischemia | Arthropathy | Biotinidase Deficiency | Conjunctivitis | Chordoma | Multiple Epiphyseal Dysplasia | Succinic Semialdehyde Dehydrogenase Deficiency | Hypertension, Renal | Facioscapulohumeral Muscular Dystrophy | Cysticercosis | Acute Lymphocytic Leukemia | Liebenberg Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Erysipelas | Gallstones | Hemangioblastoma | Carney-Stratakis Syndrome | Pulmonary Tuberculosis | Hypertension, Pulmonary | Otitis Media | WAGR Syndrome | Hypotrichosis | DRESS Syndrome | Supravalvular Aortic Stenosis | Muscle Wasting | Primrose Syndrome | Pseudohypoaldosteronism | Dermatomyositis | Menkes Disease | Lateral Meningocele Syndrome | Meningioma | Periodontitis | Neurofibroma, Plexiform | Thyroid Hormone Resistance | Primary Progressive Nonfluent Aphasia | Coloboma | Intestinal Pseudo-obstruction | Megaloblastic Anemia | Spinal Muscular Atrophy | Rett Syndrome | Lipid Metabolism Disorders | Metanephric Adenoma | 5-oxoprolinase Deficiency | Chylothorax, Congenital | Tetanus | Choroiditis | Lysosomal Acid Lipase Deficiency | Zimmermann-Laband Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Encephalopathy, Glycine | Neovascular Glaucoma | Transient Bullous Dermolysis Of The Newborn | Progressive Familial Intrahepatic Cholestasis | Optic Neuropathy, Anterior Ischemic | Hemophilia | Encephalocele | Schizencephaly | Chronic Myelomonocytic Leukemia | Retinal Dystrophy, Early-onset Severe | Syphilis | Congenital Muscular Dystrophy | Chudley-McCullough Syndrome | Hyperkalemic Periodic Paralysis | Hydrocephalus | Rhabdoid Tumor | Corneal Neovascularization | Bullous Pemphigoid | Thyroiditis, Autoimmune | Cholangitis | Neuroleptic Malignant Syndrome | Erythrokeratodermia Variabilis | Vitamin B12 Deficiency | Temtamy Preaxial Brachydactyly Syndrome | Cancer, Skin | Multicentric Carpotarsal Osteolysis Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Leukocyte Adhesion Deficiency Type 1 | Nicolaides-Baraitser Syndrome | Bulimia Nervosa | Colorectal Adenoma | Hypertrophy | 3-methylcrotonyl-CoA Carboxylase Deficiency