Intestinal Tuberculosis

About the Disease
Intestinal Tuberculosis, also known as tuberculosis of intestines, is related to intestinal obstruction and ileus, and has symptoms including abdominal pain, gastrointestinal bleeding and nausea. An important gene associated with Intestinal Tuberculosis is CRP (C-Reactive Protein), and among its related pathways/superpathways are Hematopoietic Stem Cells and Lineage-specific Markers and IL27-mediated signaling events. Affiliated tissues include intestine, small intestine and colon, and related phenotypes are endocrine/exocrine gland and immune system

Common Targets
IRGM | ATG16L1 | TNFRSF1A

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

Other Diseases

Guanidinoacetate Methyltransferase Deficiency | Salla Disease | Major Depression | Portal Vein Thrombosis | Microcephaly, Seizures, And Developmental Delay | Lipodystrophy | Analgesia | Spitzoid Melanoma | Poirier-Bienvenu Neurodevelopmental Syndrome | Hypoalbuminemia | Stuttering | Tumoral Calcinosis | Migraine | PASLI Disease | Hyperparathyroidism | Lymphoproliferative Disorders | Proopiomelanocortin Deficiency | Charcot-Marie-Tooth Disease Type 4B1 | Pure Autonomic Failure | LEOPARD Syndrome | Nicotine Dependence | Demyelinating Diseases | Kawasaki Disease | Atelosteogenesis Type 1 | Paternal Uniparental Disomy Of Chromosome 14 | Thyrotoxic Periodic Paralysis | Ameloblastoma | Congenital Diaphragmatic Hernia | Epidermolytic Palmoplantar Keratoderma | Occipital Neuralgia | Leber Congenital Amaurosis | Maple Syrup Urine Disease | Strabismus | Papillorenal Syndrome | Speech Disorders | Epithelioid Hemangioma | Situs Inversus | Granular Corneal Dystrophy | Cysticercosis | IgA Deficiency | Optic Neuropathy | Stargardt Disease | Tyrosinemia | Schamberg Disease | Renal Tubular Acidosis | Erythema Nodosum | Abetalipoproteinemia | VACTERL/VATER Association | Pseudohypoparathyroidism Type 1A | Jacobsen Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Specific Granule Deficiency | Benign Familial Infantile Seizures | Mucolipidosis Type IV | Hypertension, Renovascular | Liebenberg Syndrome | Christianson Syndrome | Chronic Beryllium Disease | Coronary Artery Disease | Nail Disorder, Nonsyndromic Congenital | Myotonic Disorders | Alpha-thalassemia Myelodysplasia Syndrome | Macrophagic Myofasciitis | Episodic Ataxia Type 1 | Chromosome 16p11.2 Deletion Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Pontocerebellar Hypoplasia | Pseudoachondroplasia | Retinoschisis | Uveitis, Anterior | Fetal Akinesia Deformation Sequence | Raine Syndrome | Amyotrophic Lateral Sclerosis | Niemann-Pick Disease, Type A | Angioedema | T-cell Prolymphocytic Leukemia | Herpes Simplex Dermatitis | Alcoholism | Polyneuropathy | Impetigo | Amenorrhea | Esophageal Adenocarcinoma | Fibronectin Glomerulopathy | Aldosteronism | Non-Hodgkin Lymphoma | Acute Chest Syndrome | Schnyder Crystalline Corneal Dystrophy | Creatine Deficiency Syndrome | Fuchs Heterochromic Iridocyclitis | Chitayat Syndrome | 3C Syndrome | Spondylo-ocular Syndrome | Feingold Syndrome | Hemimegalencephaly | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Optic Atrophy 2 | Osteomalacia | Campomelic Dysplasia | Chondrodysplasia Punctata 1, X-linked Recessive | Peeling Skin Syndrome, Acral Type | Congenital Ichthyosiform Erythroderma | Chondrodysplasia Punctata 2, X-linked Dominant | Cluster Headache | Melnick-Needles Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Anosmia, Congenital | Chorea-acanthocytosis | Sjogren Syndrome | Dubin-Johnson Syndrome | Fabry's Disease | Uveitis | Exotropia | Superficial Spreading Melanoma | Fucosidosis | Alopecia Areata | Myocarditis | McKusick Type Metaphyseal Chondrodysplasia | Kaposi Sarcoma | Sturge-Weber Syndrome | Hereditary Sensory Neuropathy Type 1 | Atrioventricular Septal Defect | Hereditary Pyropoikilocytosis | Bronchitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Creatine Deficiency Syndrome Due To AGAT Deficiency | Osteogenesis Imperfecta Type VI | Polycystic Ovary Syndrome | Chondrodysplasia Punctata | Seizures | Schizophrenia | Open-angle Glaucoma | Sick Sinus Syndrome 1 | Insulinoma | Gerodermia Osteodysplastica | Fetal Alcohol Syndrome | Macrophage Activation Syndrome | Exostoses | Craniometaphyseal Dysplasia | Amblyopia | Prolymphocytic Leukemia | Schwannomatosis | Nutrition Disorders | Iron Metabolism Disorders | Thyroid Dysgenesis | Spina Bifida | Pycnodysostosis | Triple A Syndrome | Molybdenum Cofactor Deficiency | Hepatitis D | Niemann-Pick Disease, Type C | Noonan Syndrome | Retinal Dystrophy | X-linked Acrogigantism | Ischemia | Meningococcal Infections | Cardiomyopathy, Peripartum | Lymphangiomatosis | Cardiospondylocarpofacial Syndrome | Presbycusis | Keloid | Huntington's Disease-like 2 | Tracheal Disorders | Bipolar Disorder | Bietti Crystalline Dystrophy | Charcot-Marie-Tooth Disease, Type 2 | Veno-occlusive Disease | Leukocyte Adhesion Deficiency | Ameloblastic Carcinoma | Leiomyosarcoma | T-cell Leukemia | Schizophrenia, Paranoid | Fraser Syndrome | Neuropathy | Tonsillitis | Usher Syndrome Type I | Proctitis | Schizencephaly | Jaundice, Obstructive | Chordoid Glioma | Oligospermia | Milk Allergy | Angioedema, Hereditary | Spinocerebellar Ataxia Type 3 | Gnathodiaphyseal Dysplasia | Rhizomelic Chondrodysplasia Punctata | Sporadic Inclusion Body Myositis | H Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Scoliosis | Spinocerebellar Ataxia Type 10 | Necrotizing Autoimmune Myopathy | Lichen Planus | Hereditary Elliptocytosis | Ocular Surface Squamous Neoplasia | Charcot-Marie-Tooth Disease Axonal Type 2N | Hypopigmentation | Chondromyxoid Fibroma | Familial Hypertrophic Cardiomyopathy | Steel Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Vitamin B12 Deficiency | Polycystic Kidney, Autosomal Dominant | Spondyloepiphyseal Dysplasia Tarda, X-linked | Mycosis Fungoides | Moyamoya Disease | Neurofibroma, Plexiform | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Cutaneous Mastocytosis | Warsaw Breakage Syndrome | Glaucomatocyclitic Crisis | Large Granular Lymphocytic Leukemia | Exocrine Pancreatic Insufficiency | Low Phospholipid Associated Cholelithiasis | Sensory Neuropathy | Familial Exudative Vitreoretinopathy | Colitis, Microscopic | Metanephric Adenoma | Cancer, Kidney | Oligoasthenoteratozoospermia | Von Willebrand Disease | Ollier Disease | Erythrokeratodermia Variabilis | Reye Syndrome | Peroxisomal Disorder | Enhanced S-cone Syndrome | Benign Hereditary Chorea | Smith-Magenis Syndrome | Bronchitis, Chronic | Sotos Syndrome | Syphilis | Leber Hereditary Optic Neuropathy | Protein S Deficiency | Spinal Muscular Atrophy | Goiter, Nodular | Congenital Disorders Of Glycosylation | Sertoli Cell-only Syndrome | Hyperacusis | Glucagonoma | Neuroleptic Malignant Syndrome | Chronic Granulomatous Disease, X-linked | Connective Tissue Disorders | Canavan Disease | Discoid Lupus Erythematosus | Chromosome 17q21.31 Deletion Syndrome | Eating Disorder | Paraplegia | Small Lymphocytic Lymphoma | Tardive Dyskinesia | Ichthyosis Bullosa Of Siemens | McCune-Albright Syndrome | Oculopharyngeal Muscular Dystrophy | Infantile Neuroaxonal Dystrophy | Spinal And Bulbar Muscular Atrophy | Pyelonephritis | Cystinosis | Retinal Coloboma | Anorexia Nervosa | Hermansky-Pudlak Syndrome | Pheochromocytoma | Sponastrime Dysplasia | Pineoblastoma | Sleep Disorder | Glomerulonephritis | Smoldering Myeloma | Primary Cutaneous Amyloidosis | Non-bullous Congenital Ichthyosiform Erythroderma | Metachondromatosis | Mucolipidosis | Postaxial Polydactyly | Pneumococcal Meningitis | Palsy, Cerebral | Gallstones | Photosensitivity | Acrodysostosis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Borjeson-Forssman-Lehmann Syndrome | Aspartylglycosaminuria | Sporadic Hemiplegic Migraine | Echinococcosis | Arthritis, Gouty | Hemophilia | Thromboembolism | Hypereosinophilic Syndrome | Hemorrhagic Disorders | Postpoliomyelitis Syndrome | Cousin Syndrome | Papilloma | Dyggve-Melchior-Clausen Disease | Split Hand-foot Malformation | Dysferlinopathy | Early Infantile Epileptic Encephalopathy 1 | Hyperbilirubinemia | Sandhoff Disease | Frontometaphyseal Dysplasia | Miyoshi Myopathy | Amyloidosis | Adenomyosis | Gastrointestinal Disorders | Spasticity | Adams-Oliver Syndrome | Pearson Syndrome | Spinocerebellar Ataxia | Auriculocondylar Syndrome | Restrictive Dermopathy | Rosacea | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Gliosarcoma | Hoyeraal-Hreidarsson Syndrome | Pierpont Syndrome | Atopy | Cholecystitis | Cranioectodermal Dysplasia | Temtamy Preaxial Brachydactyly Syndrome | Splenomegaly | Eclampsia | Schistosomiasis | Biotinidase Deficiency | Scleroderma | Anal Fissure | Keratosis | Behavioral Variant Of Frontotemporal Dementia | High Molecular Weight Kininogen Deficiency | Olmsted Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Riboflavin Transporter Deficiency Neuronopathy | Glycogen Storage Disease | Purpura, Thrombotic Thrombocytopenic | Androgen Insensitivity | Cole-Carpenter Syndrome | Ocular Albinism Type 1 | Tyrosinemia Type 1 | Familial Thoracic Aortic Aneurysm | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Lymphoproliferative Disease, X-linked | Lymphoma, Follicular | Stevens-Johnson Syndrome | Spinocerebellar Ataxia Type 6 | Pelvic Inflammatory Disease | Hepatitis, Alcoholic | Alkaptonuria | Bulimia Nervosa | Diabetes Insipidus, Neurogenic | Dengue Hemorrhagic Fever | Dowling-Degos Disease | Myoclonic Atonic Epilepsy | Craniolenticulosutural Dysplasia | HIBCH Deficiency | Stroke, Hemorrhagic | Krabbe Disease | Glaucoma, Congenital | Macrodactyly | Poikiloderma With Neutropenia | Pseudohypoparathyroidism Type 1C | Vestibular Disease | Rift Valley Fever | Usher Syndrome Type II | Optic Neuritis | Uremia | Platelet Disorders | Cabezas Syndrome | Geleophysic Dysplasia | Neurofibromatosis-Noonan Syndrome | Carotid Artery Disease | Benign Familial Pemphigus | Liver Failure | Hepatitis, Chronic | Huntington's Disease | Hepatoblastoma | Osteonecrosis | Otitis Externa | Bloom Syndrome | Takotsubo Cardiomyopathy | Ehlers-Danlos Syndrome | Progressive Osseous Heteroplasia | Meningitis | Iron Deficiency Anemia | Glycogen Storage Disease Type 6 | Thrombophlebitis | Addison Disease | Intermittent Explosive Disorder | Astigmatism | Saul-Wilson Syndrome | Primary Progressive Nonfluent Aphasia | Plasma Cell Dyscrasia | Metaphyseal Chondrodysplasia, Schmid Type | Blue Rubber Bleb Nevus Syndrome | Cerebrotendinous Xanthomatosis | Sarcoma, Ewing | Thanatophoric Dysplasia Type 1 | ICF Syndrome | Sick Sinus Syndrome | Microcephalic Primordial Dwarfism | Generalized Epilepsy With Febrile Seizures Plus | Renal Medullary Carcinoma | Rubinstein-Taybi Syndrome | Cerebrovascular Disorders | Craniopharyngioma | Congenital Torticollis | Spinocerebellar Ataxia Type 17