Disease

Infectious Diarrhea

About the Disease
Dysentery, also known as infectious diarrhea, is related to giardiasis and shigellosis, and has symptoms including diarrhea An important gene associated with Dysentery is ALB (Albumin), and among its related pathways/superpathways are Innate Immune System and Akt Signaling. The drugs Loperamide and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include colon, liver and small intestine, and related phenotypes are no effect and no effect

Common Targets
LOC105370481 | G4609 | TIRAP | TLR9 | NCK1 | MBL2 | CFTR | G7099 | G6774 | METAP2 | Calcium-activated chloride channel regulators (nonspecified subtype) | PDIA3 | TLR1

疾病靶点研报
Infectious Diarrhea

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

Other Diseases

Epithelial-myoepithelial Carcinoma | Lymphangiomatosis | Hepatitis, Alcoholic | Combined Pituitary Hormone Deficiency | Adenoid Cystic Carcinoma | Early Infantile Epileptic Encephalopathy 28 | Familial Digital Arthropathy-brachydactyly | Congenital Muscular Dystrophy | Subacute Sclerosing Panencephalitis | Cranial Nerve Disease | Hyperlipidemia | Chondrodysplasia Punctata 2, X-linked Dominant | Otosclerosis | Imerslund-Grasbeck Syndrome | NGLY1 Deficiency | Noonan Syndrome | Aplastic Anemia | Japanese Encephalitis | Depression | Charcot-Marie-Tooth Disease Type 4E | Iron Deficiency Anemia | Amyotrophic Lateral Sclerosis | Frontometaphyseal Dysplasia | Focal Cortical Dysplasia Type 2 | Eosinophilic Asthma | Retinal Vasculitis | Alpha-thalassemia Myelodysplasia Syndrome | Progressive Familial Intrahepatic Cholestasis | Charcot-Marie-Tooth Disease Type 2E | Uveitis | Pierson Syndrome | Silicosis | Zygomycosis | Macular Degeneration | Papillorenal Syndrome | Central Pain Syndrome | Gangliosidosis, GM1 | Anal Fissure | Congenital Central Hypoventilation Syndrome | Choroiditis | Antenatal Bartter Syndrome Type 1 | Thymoma, Malignant | Carcinoid Syndrome | Hemolytic Anemia | Hypophosphatasia | Lattice Corneal Dystrophy | Blue Rubber Bleb Nevus Syndrome | Epidermolytic Ichthyosis, Annular | DiGeorge Syndrome | Autosomal Recessive Bestrophinopathy | Mohr-Tranebjaerg Syndrome | LMNA-related Congenital Muscular Dystrophy | Tuberculous Meningitis | Neovascular Glaucoma | Antithrombin III Deficiency | Syphilis | Parkinson's Disease | Spinocerebellar Ataxia Type 28 | Mevalonate Kinase Deficiency | Aldosterone Synthase Deficiency | Leukoencephalopathy, Progressive Multifocal | Intestinal Tuberculosis | Non-Langerhans Cell Histiocytosis | Cornelia De Lange Syndrome | Adams-Oliver Syndrome | DRESS Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Pyloric Stenosis, Infantile Hypertrophic | Cantu Syndrome | Apparent Mineralocorticoid Excess Syndrome | Benign Familial Infantile Seizures | Antley-Bixler Syndrome | Peeling Skin Syndrome Type B | Richter's Syndrome | Chediak-Higashi Syndrome | Multiple Sclerosis | Dysgerminoma | Carcinoma, Merkel Cell | Macular Corneal Dystrophy | Sarcoidosis | Fatty Aldehyde Dehydrogenase Deficiency | Sarcoma, Alveolar Soft Part | Blepharoconjunctivitis | Polycystic Ovary Syndrome | Metabolic Syndrome | Spondylometaphyseal Dysplasia | Spinocerebellar Ataxia Type 20 | Rhabdomyosarcoma, Alveolar | Familial Thoracic Aortic Aneurysm | Stroke, Hemorrhagic | 3C Syndrome | Spondylocarpotarsal Synostosis Syndrome | Sleep Disorder | Agranulocytosis | Seizures | Progressive Encephalopathy-optic Atrophy Syndrome | Renal Failure | Charcot-Marie-Tooth Disease | Nasodigitoacoustic Syndrome | ADNP Syndrome | Basal Ganglia Disease | Alexander Disease | Pontocerebellar Hypoplasia Type 2 | Leber Hereditary Optic Neuropathy | Krabbe Disease | MIRAGE Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Anorchia | Cleidocranial Dysplasia | Neuroblastoma | Pulmonary Veno-occlusive Disease | Periventricular Nodular Heterotopia | Tinea Versicolor | Pneumonia, Mycoplasma | Carney Triad | Rotor Syndrome | Polyneuropathy | Long QT Syndrome Type 1 | Pilomatrix Carcinoma | Angioedema | Angioedema, Hereditary | Focal Dermal Hypoplasia | Congenital Hypofibrinogenemia | Epidermolytic Palmoplantar Keratoderma | Alkaptonuria | Asphyxia Neonatorum | Spondylo-ocular Syndrome | Lymphoma | Myoclonic Epilepsy With Ragged Red Fibers | Osteoporosis, Postmenopausal | Atherosclerosis | Lymphoproliferative Disease, X-linked | Kaposiform Hemangioendothelioma | Congenital Adrenal Hyperplasia 1 | Nemaline Myopathy 10 | Anxiety Disorders | Rhinitis | ACTH-independent Macronodular Adrenal Hyperplasia | Holoprosencephaly | Adenocarcinoma | Fetal Alcohol Syndrome | Granular Corneal Dystrophy | Hypertension | Cyclic Vomiting Syndrome | Epidermolysis Bullosa | Early Infantile Epileptic Encephalopathy | Episodic Ataxia Type 1 | Encephalopathy | Common Cold | Primary Progressive Aphasia | Familial Male-limited Precocious Puberty | Wolman Disease | Hyperammonemia | Neurofibrosarcoma | Pearson Syndrome | Pneumonia, Bacterial | Triple A Syndrome | Mood Disorder | Pancytopenia | Acute Chest Syndrome | Dermatitis Herpetiformis | Papillon-Lefevre Syndrome | Benign Familial Pemphigus | Graves Disease | Panuveitis | Progressive External Ophthalmoplegia | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Synpolydactyly | Sepiapterin Reductase Deficiency | Meniere's Disease | Methemoglobinemia Type IV | Presbycusis | Nijmegen Breakage Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Congenital Myopathy | Transient Bullous Dermolysis Of The Newborn | Familial Episodic Pain Syndrome | Hemangioendothelioma | Protein S Deficiency | Lymphedema-distichiasis Syndrome | Congenital Tufting Enteropathy | Ornithine Transcarbamylase Deficiency | Optic Atrophy 2 | Adenomatoid Tumor | Keloid | Micro Syndrome | Ameloblastoma | Waardenburg Syndrome | Vici Syndrome | Neuromyotonia | Smith-Kingsmore Syndrome | Fibrillation, Atrial | Albinism | Schnitzler Syndrome | Episodic Ataxia Type 2 | Schizoaffective Disorder | Meesmann Corneal Dystrophy | Eczema | Blepharitis | Thyroid Dyshormonogenesis | Farber Disease | Hypotension, Orthostatic | Chloridorrhea, Congenital | Congenital Diaphragmatic Hernia | Adrenoleukodystrophy, X-linked | Eiken Syndrome | Basal Ganglia Disease, Biotin-responsive | Schizophrenia | Nephritis, Interstitial | Protein C Deficiency | Thanatophoric Dysplasia | Allergic Contact Dermatitis | Myhre Syndrome | Perivascular Epithelioid Cell Tumor | Norrie Disease | Dengue Shock Syndrome | Polyradiculopathy | Proteus Syndrome | Coloboma | Crisponi Syndrome | Thyroiditis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Trichuriasis | Pitt-Hopkins Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Anterior Segment Dysgenesis | Erysipelas | Ganglioglioma | Schizotypal Personality Disorder | Immunoproliferative Disorders | Benign Recurrent Intrahepatic Cholestasis 1 | HUPRA Syndrome | Inflammatory Myofibroblastic Tumor | Dysmorphophobia | Epithelioid Hemangioma | Klinefelter Syndrome | Hypertension, Renal | Ataxia-ocular Apraxia 2 | HANAC Syndrome | Strabismus | TARP Syndrome | Porphyria, Acute Intermittent | Dent Disease | Multicystic Renal Dysplasia | Schwannoma | Lupus Erythematosus | Scleroderma, Diffuse | Thyroid Hormone Resistance | Dental Caries | Congenital Poikiloderma | Adenomyosis | Fabry's Disease | Spinocerebellar Ataxia Type 40 | Macular Corneal Dystrophy Type 1 | Pachyonychia Congenita | Guttate Psoriasis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Calcium Pyrophosphate Deposition Disease | Giant Cell Glioblastoma | Headache | Blepharo-cheilo-odontic Syndrome | Localized Scleroderma | Axenfeld-Rieger Syndrome | Mannosidase Deficiency Diseases | Porphyria, Variegate | Optic Neuropathy, Anterior Ischemic | Chronic Enteropathy Associated With SLCO2A1 Gene | Infectious Diarrhea | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Cohen Syndrome | Neurofibromatosis Type 2 | Gliosarcoma | Epilepsy, Generalized | Carcinoma, Small Cell | Autosomal Recessive Spastic Paraplegia Type 35 | Exfoliative Dermatitis | Diabetes Type 2 | Ependymoma | Senior-Loken Syndrome | Chylomicron Retention Disease | Systemic Mastocytosis | T-cell Lymphoma, Subcutaneous Panniculitis-like | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Hidradenitis | Postpartum Depression | Glycogen Storage Disease Type 6 | Charcot-Marie-Tooth Disease Axonal Type 2N | Lipid Storage Myopathy | Thin Basement Membrane Disease | Trichomegaly | Congenital Hereditary Endothelial Dystrophy Type II | Sialidosis Type I | Seborrheic Dermatitis | Nestor-Guillermo Progeria Syndrome | Fibrosis | Tyrosine Hydroxylase Deficiency | Marinesco-Sjogren Syndrome | Hepatitis D | Premature Ejaculation | Epiphyseal Chondrodysplasia, Miura Type | Pemphigus Foliaceus | Saethre-Chotzen Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Allan-Herndon-Dudley Syndrome | Hepatic Veno-occlusive Disease | Nephrocalcinosis | Intracranial Hypertension | Cervicitis | Multiple Sclerosis, Secondary Progressive | Prolidase Deficiency | Systemic Lupus Erythematosus | Sertoli Cell-only Syndrome | Craniofacial Dysostosis | Chorea-acanthocytosis | Antisynthetase Syndrome | Hereditary Multiple Exostoses | Retinal Detachment | Johanson-Blizzard Syndrome | Heterotopic Ossification | Rothmund-Thomson Syndrome | Impetigo | Myofibromatosis | Conduct Disorder | Skin Fragility-woolly Hair Syndrome | Neurofibromatosis | Hypocalcemia | Osteogenesis Imperfecta Type III | Progressive Osseous Heteroplasia | Congenital Torticollis | Chondrosarcoma | Carney-Stratakis Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Nail-Patella Syndrome | GM2-gangliosidosis AB Variant | Hepatorenal Syndrome | Zellweger Syndrome | Schizophrenia, Paranoid | Coffin-Siris Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Hereditary Coproporphyria | Hypobetalipoproteinemias | Tuberculosis | Gestational Trophoblastic Disease | Cholestasis | Plasma Cell Dyscrasia | Rheumatic Heart Disease | Atelosteogenesis Type 1 | Thrombosis | Schizencephaly | Infantile Liver Failure Syndrome 1 | Sjogren Syndrome | Hernia, Inguinal | Kaposi Sarcoma | Restrictive Dermopathy | Phosphoglycerate Dehydrogenase Deficiency | Transcobalamin Deficiency | Infantile Spasm | Dominant Optic Atrophy | Glanzmann Thrombasthenia | Withdrawal Syndrome | Xeroderma Pigmentosum | Hyperthermia, Malignant | B-cell Prolymphocytic Leukemia | Pulmonary Vein Stenosis | Myotonia | Superficial Spreading Melanoma | Genee-Wiedemann Syndrome | Ocular Albinism Type 1 | Lysosomal Acid Lipase Deficiency | COACH Syndrome | Sorsby Fundus Dystrophy | Nail Disorder, Nonsyndromic Congenital | Androgen Insensitivity | Treacher Collins Syndrome | Primary Hyperoxaluria | Leukodystrophies | Cerebellofaciodental Syndrome | Optic Neuritis | Cardiomyopathy, Dilated, 1L | Hypereosinophilic Syndrome | Cancer, Colon | Pulverulent Zonular Cataract | Avellino Corneal Dystrophy | Sick Sinus Syndrome | Growth Hormone Excess | Polymyalgia Rheumatica | Juvenile Myoclonic Epilepsy | Long QT Syndrome Type 3 | Myelofibrosis | Cancer, Kidney | Vitamin K Deficiency | Glomerulonephritis, Membranous | Autosomal Recessive Spastic Paraplegia Type 75 | Vitelliform Macular Dystrophy | Myoclonus | Coffin-Lowry Syndrome | Familial Hypobetalipoproteinemia | Malonyl-CoA Decarboxylase Deficiency | Acne | Parvovirus B19 Infection