Cholera
Cholera
About the Disease
Cholera, also known as vibrio cholerae infection, is related to pertussis and colon adenocarcinoma, and has symptoms including fever and pruritus. An important gene associated with Cholera is ARF1 (ADP Ribosylation Factor 1), and among its related pathways/superpathways are Metabolism and Disease. The drugs Mycophenolic acid and Prednisolone phosphate have been mentioned in the context of this disorder. Affiliated tissues include small intestine, skin and spinal cord, and related phenotypes are diarrhea and hypotension
Common Targets
CA1 | CA12 | CA7 | CA14 | CA9 | CA2 | CFTR | GNAS
Note: If you'd like to get a target analysis report for Cholera, 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 Cholera at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Retinopathy, Diabetic | Fibromyalgia | Chronic Lymphocytic Leukemia | Hyperlipidemia Type V | Episodic Ataxia | Syphilis | Arthritis, Reactive | Actinomycetoma | Membranous Nephropathy | Stromal Corneal Dystrophy | Neonatal Progeroid Syndrome | Alazami Syndrome | Chronic Granulomatous Disease | Measles | Multiple System Atrophy | T-cell Prolymphocytic Leukemia | Tumoral Calcinosis | Kleine-Levin Syndrome | Peritonitis | Alveolar Capillary Dysplasia | Portal Vein Thrombosis | Eclampsia | Hyperinsulinism-hyperammonemia Syndrome | Acrodermatitis | Hartsfield Syndrome | Conjunctivitis, Allergic | Scleritis | Twin-to-twin Transfusion Syndrome | Dystonia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Glycogen Storage Disease Type 9 | Dwarfism | Lattice Corneal Dystrophy | Cerebrotendinous Xanthomatosis | Cryptorchidism | Arterial Tortuosity Syndrome | Coronary Heart Disease | Usher Syndrome Type IIC | Chondrodysplasia Punctata | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Familial Isolated Hyperparathyroidism | Hyper IgE Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Spinal Muscular Atrophy Type 2 | Crohn's Disease | Hyperbilirubinemia | Mucormycosis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Infantile Refsum Disease | Pseudoachondroplasia | Anosmia, Congenital | Ichthyosis | DICER1 Syndrome | Lymphangioleiomyomatosis | Connective Tissue Disorders | Acute Myeloid Leukemia | Rhinitis | Focal Dermal Hypoplasia | Usher Syndrome Type I | Myoclonic Atonic Epilepsy | Hyperprolactinemia | Atelosteogenesis Type 2 | Osteoporosis, Postmenopausal | Long QT Syndrome Type 3 | Oral Lichen Planus | Metatropic Dysplasia | Spondylolisthesis | Angina Pectoris | Medulloblastoma | Gynecomastia | Polycystic Liver | Multiple Sclerosis, Primary Progressive | Craniosynostosis | Persistent Truncus Arteriosus | Headache | VACTERL/VATER Association | Budd-Chiari Syndrome | Oculocutaneous Albinism Type 2 | Danon Disease | Antithrombin III Deficiency | Zimmermann-Laband Syndrome | C3 Glomerulonephritis | Loeys-Dietz Syndrome | Relapsing Polychondritis | Hereditary Pyropoikilocytosis | Hepatopulmonary Syndrome | N-acetylglutamate Synthase Deficiency | Coloboma | Hyperkalemic Periodic Paralysis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Kashin-Beck Disease | Pantothenate Kinase-associated Neurodegeneration | Meningeal Melanocytoma | Retinitis Pigmentosa 3 | Fundus Albipunctatus | Thin Basement Membrane Disease | Hemophilia | Chronic Idiopathic Myelofibrosis | Carcinoma, Transitional Cell | Osteoarthritis | Hypertelorism | Cryptosporidiosis | Adenoid Cystic Carcinoma | Erythematotelangiectatic Rosacea | Glaucoma | Wolcott-Rallison Syndrome | Sorsby Fundus Dystrophy | Dentinogenesis Imperfecta | Chronic Kidney Disease | Wagner Disease | Central Core Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Inflammatory Linear Verrucous Epidermal Nevus | Periodontitis | Alagille Syndrome | Astigmatism | Esophagitis, Eosinophilic | Presbycusis | Papillon-Lefevre Syndrome | Atelosteogenesis Type 1 | Astrocytoma | Goiter, Nodular | Panuveitis | Neurotoxicity | Craniopharyngioma | Tyrosinemia | Lipid Metabolism Disorders | Schizencephaly | Hypotonia-cystinuria Syndrome | Parapsoriasis | Polyomavirus Nephropathy | Cornelia De Lange Syndrome | Erdheim-Chester Disease | Alstrom Syndrome | Hyperoxaluria | Pyloric Stenosis, Infantile Hypertrophic | Usher Syndrome Type III | Angiosarcoma Of The Breast | Dermatitis | Ameloblastoma | Hepatitis | Congenital Muscular Dystrophy | Early Infantile Epileptic Encephalopathy 4 | Antisynthetase Syndrome | Neutropenia | Charcot-Marie-Tooth Disease Type 2E | Coenzyme Q10 Deficiency | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hemolytic Uremic Syndrome, Atypical | Tendinitis | Carcinoid Tumor | Bardet-Biedl Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Still Disease | Leukoencephalopathy, Progressive Multifocal | Ectrodactyly | Primary Lateral Sclerosis | Cancer, Kidney | Dupuytren Disease | Vitreoretinopathy, Proliferative | Endometriosis | Trismus-pseudocamptodactyly Syndrome | Spinocerebellar Ataxia Type 10 | 3-methylglutaconic Aciduria Type I | Saethre-Chotzen Syndrome | DOCK8 Immunodeficiency Syndrome | Benign Familial Infantile Seizures | Waardenburg Syndrome Type 2E | Acral Lentiginous Melanoma | ADNP Syndrome | Hereditary Folate Malabsorption | Aneurysm, Thoracic Aortic | Nephronophthisis | Cervical Dystonia | High Molecular Weight Kininogen Deficiency | Juvenile Hyaline Fibromatosis | Pregnancy, Ectopic | Carbonic Anhydrase VA Deficiency | Carcinoma, Small Cell | DiGeorge Syndrome | Raine Syndrome | Cysticercosis | Hyperlipidemia | Trachoma | Megalencephaly | Histiocytic Sarcoma | Polycythemia | Mevalonate Kinase Deficiency | Rubinstein-Taybi Syndrome | Focal Facial Dermal Dysplasia | Subacute Sclerosing Panencephalitis | Thyrotoxic Periodic Paralysis | Granular Corneal Dystrophy | Renal Tubular Acidosis | Phosphoglycerate Dehydrogenase Deficiency | Pityriasis Rubra Pilaris | Diabetes Type 1 | Mucolipidosis | Leiomyoma | Spinocerebellar Ataxia Type 42 | Sponastrime Dysplasia | Thyroiditis | Keratocystic Odontogenic Tumor | Myofibrillar Myopathy | Campomelic Dysplasia | Hepatitis E | Pigment Dispersion Syndrome | Spinal Muscular Atrophy | Nemaline Myopathy 8 | Lissencephaly 2 | Liver Diseases | Hydrolethalus Syndrome | Carpenter Syndrome | Leukodystrophies | Hernia, Inguinal | Dyskeratosis Congenita | Mabry Syndrome | Cleidocranial Dysplasia | Spondyloarthritis | Fascioliasis | Cerebral Amyloid Angiopathy | Myocarditis | Glycogen Storage Disease Type 6 | Traboulsi Syndrome | Congenital Disorders Of Glycosylation Type II | Anovulation | Stickler Syndrome | Wiedemann-Steiner Syndrome | Isovaleric Acidemia | Charcot-Marie-Tooth Disease, Type 2C | Hyperacusis | Peeling Skin Syndrome, Acral Type | Common Cold | Thanatophoric Dysplasia Type 1 | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Aarskog-Scott Syndrome | Haim-Munk Syndrome | Pearson Syndrome | Mitochondrial DNA Depletion Syndrome | Persistent Hyperplastic Primary Vitreous | Ataxia-ocular Apraxia 2 | Carbohydrate Metabolism Disorders | Cystitis, Interstitial | Exocrine Pancreatic Insufficiency | Spinocerebellar Ataxia Type 6 | Paget's Disease Of The Breast | Werner's Syndrome | Craniometaphyseal Dysplasia | Combined Malonic And Methylmalonic Acidemia | Spondyloperipheral Dysplasia | Gilbert Syndrome | Disseminated Intravascular Coagulation | Schistosomiasis Mansoni | Nance-Horan Syndrome | Dyslexia | Choroideremia | Peripheral T-cell Lymphoma | Trichuriasis | Retinal Vasculitis | Corneal Edema | Epidermolysis Bullosa Dystrophica | GM2-gangliosidosis AB Variant | Fukuyama Congenital Muscular Dystrophy | Hyperbilirubinemia, Neonatal | Anorchia | Plasma Cell Dyscrasia | Hypophosphatasia | Vulvovaginitis | Chronic Enteropathy Associated With SLCO2A1 Gene | Diarrhea | Joubert Syndrome | Disseminated Superficial Actinic Porokeratosis | Progressive Familial Intrahepatic Cholestasis | Cancer, Prostate | Prostatitis | Arthritis, Gouty | Mohr-Tranebjaerg Syndrome | Schizophrenia | Spinocerebellar Ataxia Type 27 | Trigonocephaly | Chromosome 17q21.31 Deletion Syndrome | Intestinal Obstruction | Pancytopenia | Hypertensive Retinopathy | Allergic Contact Dermatitis | Epidermolysis Bullosa Simplex | Basan Syndrome | Corneal Dystrophies, Hereditary | Congenital Nystagmus | Contact Dermatitis | Cabezas Syndrome | Stroke | Giant Cell Glioblastoma | Neurodevelopmental Disorders | Borjeson-Forssman-Lehmann Syndrome | Galactosialidosis | Toxoplasmosis | Spitzoid Melanoma | Gerstmann-Straussler-Scheinker Syndrome | Conduct Disorder | Chronic Myeloid Leukemia | Congenital Bilateral Absence Of Vas Deferens | Gastrointestinal Disorders | Xeroderma Pigmentosum | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Lymphomatoid Granulomatosis | Benign Familial Pemphigus | Hypothyroidism | 3-methylglutaconic Aciduria | Spasticity | Infertility, Male | Arteriosclerosis | Familial Exudative Vitreoretinopathy | Antisocial Personality Disorder | Gitelman Syndrome | Saul-Wilson Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Congenital Poikiloderma | Beckwith-Wiedemann Syndrome | Peters-plus Syndrome | Pilomatrix Carcinoma | Persistent Fetal Circulation | Palmoplantar Keratoderma | Congenital Hereditary Endothelial Dystrophy Type I | Schuurs-Hoeijmakers Syndrome | Mitochondrial Cytopathy | Chondrosarcoma | Pure Red Cell Aplasia | Muckle-Wells Syndrome | Onchocerciasis | Pain | Renal Oncocytoma | Congenital Dysfibrinogenemia | Rhabdomyosarcoma, Embryonal | Charcot-Marie-Tooth Disease, Type 2 | Huntington's Disease-like 2 | Astrocytoma, Anaplastic | Hyperparathyroidism, Secondary | Melanoma, Uveal | Lymphoma, AIDS-related | Hypohidrotic Ectodermal Dysplasia | Cutaneous Angiosarcoma | Von Hippel-Lindau Disease | Constipation | Carcinoid Syndrome | Thrombocytopenia | Premature Ejaculation | Arts Syndrome | Pierson Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Spinocerebellar Ataxia Type 28 | Non-proliferative Diabetic Retinopathy | Encephalopathy, Ethylmalonic | Cousin Syndrome | Kaposi Sarcoma | Delayed Sleep Phase Syndrome | GAPO Syndrome | Focal Cortical Dysplasia Type 2 | Fibrillation, Atrial | Overactive Bladder | Paraganglioma, Carotid Body | Cutaneous Mastocytosis | Stevens-Johnson Syndrome | Majeed Syndrome | Spinal And Bulbar Muscular Atrophy | Optic Atrophy 2 | Endophthalmitis | Interstitial Lung Diseases | Goldenhar Syndrome | Juvenile Xanthogranuloma | Porphyria Cutanea Tarda | Reye Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Microtia | Spinocerebellar Ataxia Type 2 | Polyradiculopathy | Metabolic Syndrome | Hypogammaglobulinemia | Methylmalonic Acidemia | Spermatocele | Primary Hyperoxaluria | Alpha-mannosidosis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Primrose Syndrome | Cerebral Cavernous Malformations | Acute Leukemia | Glutaric Aciduria Type 2 | Ileitis | Fibromuscular Dysplasia | Glycogen Storage Disease Type 1b | Vitamin A Deficiency | Vitreoretinal Degeneration, Snowflake Type | Amyotrophic Lateral Sclerosis | Renal Medullary Carcinoma | Lymphopenia | Myelitis | Insulin Resistance | Sick Sinus Syndrome | Subcortical Band Heterotopia | Congenital Aniridia