Schistosomiasis

About the Disease
Intestinal Schistosomiasis, also known as schistosomiasis japonica, is related to schistosomiasis and neuroschistosomiasis. An important gene associated with Intestinal Schistosomiasis is IL13 (Interleukin 13), and among its related pathways/superpathways are Akt Signaling and PAK Pathway. The drugs Lumefantrine and Artemether have been mentioned in the context of this disorder. Affiliated tissues include liver, t cells and spleen, and related phenotypes are immune system and no phenotypic analysis

Common Targets
PSMB5 | PTGS1 | TYR | STAT6 | G7295 | HDAC8 | TGFBR1 | DHODH | IL1B | GALE | G7124 | IL1RL1 | PFDN4 | SRP54 | PGRMC2 | NR1H4 | CTLA4 | MASP2 | Chaperone (nonspecified subtype) | Histone acetyltransferase (HAT) (nonspecified subtype) | FAAH | MBL2 | ELAVL1 | NOX3 | ZNF503-AS1 | APOE | Cysteine Protease (nonspecified subtype) | PNP | CREBBP | G7099 | NADPH Oxidase Complex | KAT2A | IL13 | GPX4 | G6774 | NADPH Oxidase (nonspecified subtype) | HIF1A | HDAC6 | KAT2B | GSR | FCN2 | MAOA | AVPR1A | ATP1A1 | STAT6 | PRKCA | ALDH3A2 | CACNA1D | KCNJ5 | IL10 | ATP2B3 | CTNNB1 | CYP11B2 | CACNA1H

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

Other Diseases

Ocular Surface Squamous Neoplasia | Epidermolytic Palmoplantar Keratoderma | Aplasia Cutis Congenita | Osteoporosis | Omenn Syndrome | Hemorrhagic Disorders | Hartsfield Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Optic Neuropathy, Anterior Ischemic | Stroke | Woodhouse-Sakati Syndrome | Goldenhar Syndrome | Potocki-Shaffer Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Diabetic Nephropathy | MELAS Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | H Syndrome | Neutrophilia | Cancer, Brain | Lennox-Gastaut Syndrome | Localized Scleroderma | T-cell Leukemia | Choriocarcinoma | Tonsillitis | Fundus Albipunctatus | Malnutrition | Niemann-Pick Disease, Type C | Viral Meningitis | Spinocerebellar Ataxia Type 5 | Plasmacytoma | Arterial Tortuosity Syndrome | Ellis-Van Creveld Syndrome | Early Infantile Epileptic Encephalopathy 4 | Dyggve-Melchior-Clausen Disease | Microphthalmia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Cholelithiasis | McKusick Type Metaphyseal Chondrodysplasia | Asperger Syndrome | Lymphoma | Charcot-Marie-Tooth Disease Type 4B1 | Atrial Septal Defect | Hypopigmentation | Xeroderma Pigmentosum | Achromatopsia | Colitis, Collagenous | Usher Syndrome | Gaucher Disease | Hypertension, Renovascular | Peripheral T-cell Lymphoma | Isovaleric Acidemia | Ulcerative Colitis | Nicotine Dependence | Acne | Greenberg Dysplasia | Thyrotoxic Periodic Paralysis | Congenital Myasthenic Syndrome | COACH Syndrome | Acral Lentiginous Melanoma | Charcot-Marie-Tooth Disease Type 4E | Intestinal Hypomagnesemia 1 | Pneumonia, Mycoplasma | Blastoma, Pleuropulmonary | Congenital Aniridia | Congenital Afibrinogenemia | Inborn Errors Of Metabolism | Cholera | Autosomal Recessive Congenital Ichthyosis | Congenital Adrenal Hyperplasia 1 | Tetanus | C3 Glomerulonephritis | Vertebrobasilar Insufficiency | Apert Syndrome | Mycosis Fungoides | Gyrate Atrophy Of The Choroid And Retina | Multiple Sulfatase Deficiency | Long QT Syndrome Type 1 | Mitochondrial Cytopathy | Neurocutaneous Syndromes | Epidermolysis Bullosa Simplex, Localized | Uveitis, Anterior | Tay-Sachs Disease | Ileitis | Glycogen Storage Disease Type 3 | Gout | Systemic Lupus Erythematosus | Hereditary Multiple Exostoses | Glomerulonephritis, Membranous | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Low Phospholipid Associated Cholelithiasis | Lysosomal Acid Lipase Deficiency | Partington Syndrome | Sepiapterin Reductase Deficiency | Progressive Myoclonic Epilepsy | Anti-NMDA Receptor Encephalitis | Hypotension, Orthostatic | Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia | Epilepsy | Myasthenia | Rotor Syndrome | Spinocerebellar Ataxia Type 40 | Thymoma, Malignant | Hypersensitivity | Enhanced S-cone Syndrome | Camptocormia | Bronchitis, Chronic | Generalized Epilepsy With Febrile Seizures Plus | Granuloma Annulare | Restrictive Dermopathy | Fucosidosis | Paget's Disease Of The Breast | Osteoporosis-pseudoglioma Syndrome | Dysthymia | Glycogen Storage Disease Type 9 | Gastritis | Graft-versus-host Disease | Li-Fraumeni Syndrome | Thromboembolism | Adrenoleukodystrophy, X-linked | Pulmonary Sclerosing Hemangioma | Smith-Magenis Syndrome | Dermatomyositis | Pyruvate Dehydrogenase Deficiency | Necrobiosis Lipoidica | Erectile Dysfunction | Peroxisomal Disorder | Supravalvular Aortic Stenosis | Otitis Externa | Pitt-Hopkins Syndrome | Cardiomyopathy, Peripartum | Alpha-mannosidosis | Narcolepsy | Basan Syndrome | Ichthyosis, X-linked | Pulmonary Alveolar Microlithiasis | Chronic Myelomonocytic Leukemia | Meesmann Corneal Dystrophy | Congenital Absence Of Vas Deferens | Keratoacanthoma | Bruck Syndrome | Neuroendocrine Cancer | Stevens-Johnson Syndrome | Polyneuropathy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Cholesteryl Ester Storage Disease | Parkinson Disease 6, Autosomal Recessive Early-onset | Hypodontia | Adenomyosis | Specific Granule Deficiency | Multiple Sclerosis | Bone Marrow Necrosis | Metanephric Adenoma | Bicuspid Aortic Valve | Headache | Sjogren Syndrome | POEMS Syndrome | Pemphigus Foliaceus | Wagner Disease | Cenani-Lenz Syndactyly Syndrome | Myoclonus | Castleman Disease | Herpes Genitalis | Spitzoid Melanoma | Chronic Inflammatory Demyelinating Polyneuropathy | Basal Ganglia Disease | Acute Anterior Uveitis | Pseudohypoparathyroidism Type 2 | Schizoaffective Disorder | Eating Disorder | Myofibrillar Myopathy | Hereditary Elliptocytosis | Glycogen Storage Disease Type 4 | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Thyroid Dyshormonogenesis | Spondylolisthesis | Oligoastrocytoma | Peeling Skin Syndrome, Acral Type | Chromosome 16p11.2 Deletion Syndrome | Anti-glomerular Basement Membrane Disease | 3C Syndrome | Retinoschisis | Sleep Apnea, Obstructive | Renal Medullary Carcinoma | Cartilage Disorders | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Peyronie's Disease | Galactosialidosis | Whipple's Disease | Arthritis, Psoriatic | Lymphedema-distichiasis Syndrome | Acute Motor Axonal Neuropathy | Schistosomiasis | Chronic Granulomatous Disease, X-linked | Neurofibroma | Cerebral Amyloid Angiopathy | Renal Hypouricemia | Still Disease | Meleda Disease | Otopalatodigital Syndrome Type 2 | Pericarditis | Shwachman-Bodian-Diamond Syndrome | Hydrocephalus | Chromosome 8q21.11 Deletion Syndrome | Multicystic Renal Dysplasia | T-cell Prolymphocytic Leukemia | Chorioretinitis | Pontocerebellar Hypoplasia Type 2 | Focal Facial Dermal Dysplasia | Bainbridge-Ropers Syndrome | Overactive Bladder | Bronchitis | Renal-hepatic-pancreatic Dysplasia | Adenomatoid Tumor | Blepharoconjunctivitis | Non-small Cell Lung Cancer | Exotropia | Hypoplastic Left Heart Syndrome | Thrombosis | Noonan Syndrome | Vici Syndrome | Mixed Connective Tissue Disease | Melanoma, Uveal | Benign Hereditary Chorea | Measles | Ophthalmia, Sympathetic | Tyrosinemia Type 2 | Neurotoxicity | Dystrophy, Cone-rod | Sarcosinemia | Glioma | Meningioma | Cranioectodermal Dysplasia | Hairy Cell Leukemia | VACTERL Association | Subacute Sclerosing Panencephalitis | Dysmorphophobia | Episodic Ataxia Type 2 | Binge Eating Disorder | Huntington's Disease | Arteriosclerosis | Lichen Sclerosus | Pseudoexfoliation Syndrome | Osteosclerosis | Cat Eye Syndrome | Conduct Disorder | Schnyder Crystalline Corneal Dystrophy | Lesch-Nyhan Syndrome | Anorexia Nervosa | Iron Metabolism Disorders | Hypoproteinemia, Hypercatabolic | Polymyositis | Nicotine Addiction | Trichothiodystrophy | Chondroma | Porphyria | Dermatitis Herpetiformis | Polymicrogyria | Tetraplegia | Idiopathic Pulmonary Fibrosis | Amish Infantile Epilepsy Syndrome | VACTERL/VATER Association | Cabezas Syndrome | Coenzyme Q10 Deficiency | Keratocystic Odontogenic Tumor | Palsy, Cerebral | Pineoblastoma | Apraxia | Shock, Cardiogenic | Cutaneous Angiosarcoma | Optic Neuritis | Spinocerebellar Ataxia Type 12 | Carcinoma, Merkel Cell | Epiphyseal Chondrodysplasia, Miura Type | Chromosome 5q Deletion Syndrome | Cellulitis | Tricho-hepato-enteric Syndrome | Cerebellofaciodental Syndrome | Papillorenal Syndrome | Chronic Idiopathic Myelofibrosis | HANAC Syndrome | Sarcomatoid Carcinoma Of The Lung | Malignant Peripheral Nerve Sheath Tumor | Hernia, Inguinal | Congestive Heart Failure | Progressive Osseous Heteroplasia | Congenital Hypofibrinogenemia | Spermatocele | Primary Cutaneous Amyloidosis | Weill-Marchesani Syndrome | Klippel-Feil Syndrome | Azoospermia | Congenital Tufting Enteropathy | LRBA Deficiency | Sclerosteosis | Autonomic Neuropathy | Polyomavirus Nephropathy | Purpura | Lipodystrophy | Thrombocythemia, Essential | Osteomalacia | Peripheral Neuropathy | Stuttering | Keratosis, Actinic | Anovulation | Corticobasal Syndrome | Toxoplasmosis | Citrullinemia | Wolff-Parkinson-White Syndrome | Gangliosidosis, GM1 | Esophageal Adenocarcinoma | Congenital Nephrotic Syndrome | Peters-plus Syndrome | N-acetylglutamate Synthase Deficiency | Pyruvate Kinase Deficiency | Neuroectodermal Tumors, Primitive | Sarcoidosis, Pulmonary | Carcinoid Syndrome | Lymphedema | Microphthalmia, Syndromic 7 | Endometrial Hyperplasia | Chylomicron Retention Disease | Congenital Bilateral Absence Of Vas Deferens | Nephronophthisis | Wolfram Syndrome 2 | Ligneous Conjunctivitis | Peritonitis | Early Infantile Epileptic Encephalopathy | Neurofibromatosis Type 2 | Porphyria, Variegate | Mabry Syndrome | Cataplexy | Diffuse Mesangial Sclerosis | Vitelliform Macular Dystrophy | Ependymoma | Prediabetes | Noonan Syndrome-like Disorder With Loose Anagen Hair | Pleomorphic Xanthoastrocytoma | Corneal Ulcer | Spina Bifida | Kaposiform Hemangioendothelioma | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | 5-oxoprolinase Deficiency | Double Outlet Right Ventricle | Agoraphobia | Farber Disease | GNE Myopathy | Auriculocondylar Syndrome | Sick Sinus Syndrome 1 | Goiter | Ectopia Lentis, Isolated, Autosomal Recessive | Hypospadias | Agnathia-Otocephaly Complex | Acute Lung Injury | Neural Tube Defect | Hypocalcemia | Congenital Torticollis | CDKL5 Deficiency Disorder | CREST Syndrome | Rift Valley Fever | Bethlem Myopathy | Dent Disease | Hyperekplexia | Brachydactyly | Leukocyte Adhesion Deficiency Type 1 | Carcinoma, Small Cell | Impetigo | Inflammatory Joint Disease | Posterior Polar Cataract | Episodic Ataxia Type 1 | Thanatophoric Dysplasia | Adenocarcinoma | Seizures | Wieacker-Wolff Syndrome | Presbyopia | Glutaric Aciduria Type 3 | Menkes Disease | Gastritis, Atrophic | Juvenile Xanthogranuloma | Epicondylitis | Postpoliomyelitis Syndrome | Hypereosinophilic Syndrome | Spinocerebellar Ataxia Type 15 | Leber Hereditary Optic Neuropathy | Prader-Willi Syndrome | Hyperlipidemia, Familial Combined | Paronychia | Occipital Neuralgia | Cleidocranial Dysplasia | Hyperinsulinism-hyperammonemia Syndrome | Intracranial Hypertension | Thrombasthenia | Hermansky-Pudlak Syndrome | Osteochondroma | Wilson's Disease | Spinocerebellar Ataxia Type 27 | Trachoma | Renal Oncocytoma | Non-Hodgkin Lymphoma