Disease

Whipple's Disease

About the Disease
Whipple Disease, also known as intestinal lipodystrophy, is related to olecranon bursitis and gastroenteritis. An important gene associated with Whipple Disease is IRF4 (Interferon Regulatory Factor 4), and among its related pathways/superpathways are Hematopoietic Stem Cells and Lineage-specific Markers and Innate Lymphoid Cells Differentiation. Affiliated tissues include heart, brain and lung, and related phenotypes are developmental regression and arthritis

Common Targets
G3569

疾病靶点研报
Whipple's Disease

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

Other Diseases

Nephrotic Syndrome | Small Lymphocytic Lymphoma | Aarskog-Scott Syndrome | Cerebral Amyloid Angiopathy | Hereditary Sensory And Autonomic Neuropathy | Greig Cephalopolysyndactyly Syndrome | Meckel-Gruber Syndrome | Spinocerebellar Ataxia Type 42 | Poirier-Bienvenu Neurodevelopmental Syndrome | Campomelic Dysplasia | Early Infantile Epileptic Encephalopathy 4 | Kaposi Sarcoma | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | PHARC Syndrome | Porphyria Cutanea Tarda | Schindler Disease | Motion Sickness | Nicolaides-Baraitser Syndrome | Supravalvular Aortic Stenosis | Adrenoleukodystrophy, X-linked | Globozoospermia | Cutaneous Mastocytosis | Diastrophic Dysplasia | Oculocutaneous Albinism Type 2 | VEXAS Syndrome | Omenn Syndrome | Esophageal Motility Disorders | Sclerocornea | Hypophosphatasia | Iron Overload | Guillain-Barre Syndrome | Blepharo-cheilo-odontic Syndrome | Duodenal Atresia | Juvenile Hyaline Fibromatosis | Megalencephaly | Hepatitis, Autoimmune | Obsessive-compulsive Disorder | Pneumothorax | Cutaneous T-cell Lymphoma | Nanophthalmos | Bartsocas-Papas Syndrome | Pouchitis | Neural Tube Defect | Pyruvate Carboxylase Deficiency Disease | Chromosome 17q21.31 Deletion Syndrome | B-cell Prolymphocytic Leukemia | Glycogen Storage Disease Type 1 | Thrombotic Microangiopathy | Dermatofibrosarcoma | Dentinogenesis Imperfecta | Dent Disease | Oculopharyngeal Muscular Dystrophy | Hemorrhage | Carcinoid Tumor | Borjeson-Forssman-Lehmann Syndrome | Waardenburg Syndrome Type 1 | Glycogen Storage Disease Type 0 | Distal Spinal Muscular Atrophy | Goiter, Nodular | Keratocystic Odontogenic Tumor | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Chorea | Hepatitis, Chronic | Craniosynostosis | Periodontitis | Seizures | T-cell Chronic Lymphocytic Leukemia | Myositis, Focal | Diabetes Gestational | Cryoglobulinemia | Spinal Muscular Atrophy Type 2 | Diabetes Mellitus, Transient Neonatal | Pre-eclampsia | Raynaud Phenomenon | Tracheal Disorders | Hyperlipidemia Type V | Adenocarcinoma | Neuromyotonia | Multiple Epiphyseal Dysplasia | Inflammatory Myofibroblastic Tumor | Leigh Syndrome | Congenital Nephrotic Syndrome | Congenital Bilateral Absence Of Vas Deferens | Acute Motor Axonal Neuropathy | Anorectal Fistula | Diabetic Nephropathy | Multicentric Carpotarsal Osteolysis Syndrome | Acute Anterior Uveitis | Membranous Nephropathy | Spinocerebellar Ataxia Type 15 | Congenital Disorders Of Glycosylation | Osteoporosis-pseudoglioma Syndrome | Mountain Sickness | Kabuki Syndrome 2 | Smith-Lemli-Opitz Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Endometrial Hyperplasia | Spinocerebellar Ataxia Type 40 | Split Hand-foot Malformation | Miyoshi Myopathy | Cholecystitis | Sick Sinus Syndrome 1 | Hypereosinophilic Syndrome | Hypercalciuria | Acute Coronary Syndrome | Vitamin D Deficiency | Binge Eating Disorder | Orthostatic Intolerance | Pyruvate Decarboxylase Deficiency | SAPHO Syndrome | Pseudohypoparathyroidism Type 1A | Juvenile Polyposis | Woodhouse-Sakati Syndrome | Bronchitis, Chronic | Vertebrobasilar Insufficiency | Learning Disability | Holt-Oram Syndrome | Overactive Bladder | C3 Glomerulopathy | Hereditary Inclusion Body Myopathy | Brooke-Spiegler Syndrome | Hemorrhagic Disorders | Nephrosclerosis | Sarcosinemia | Neutropenia | Peripheral T-cell Lymphoma | Metabolic Syndrome | Glutaric Aciduria Type 1 | Shock, Cardiogenic | Situs Inversus | Lymphoma, AIDS-related | Benign Familial Neonatal Convulsions | Constipation | Myasthenia Gravis | Peroxisomal Disorder | Congenital Stationary Night Blindness | Periodic Limb Movement Disorder | Acute Lymphocytic Leukemia | Sarcoma, Ewing | Lymphangioleiomyomatosis | Cancer, Kidney | Nephritis, Interstitial | HANAC Syndrome | Primary Aldosteronism | Imerslund-Grasbeck Syndrome | Myoclonus-dystonia Syndrome | Portal Vein Thrombosis | Polyradiculopathy | Alazami Syndrome | Colitis, Lymphocytic | Urticaria | Acute Generalized Exanthematous Pustulosis | Familial Partial Lipodystrophy | Gastrointestinal Disorders | Epilepsy | Purpura | Esotropia | Retinal Vasculitis | Epidermolysis Bullosa Simplex, Localized | Hypodontia | Ichthyosis, X-linked | Hyperlipidemia, Familial Combined | Spinocerebellar Ataxia Type 38 | Chorioretinitis | Acute Tubular Necrosis | Sleep Disorder | Influenza | Autoimmune Disease | Pneumoconiosis | Dwarfism | Pulverulent Zonular Cataract | Colorectal Adenoma | Barakat Syndrome | Prune Belly Syndrome | Nephropathy | Thalassemia | Galloway-Mowat Syndrome | Weill-Marchesani Syndrome | Triple A Syndrome | Rhabdoid Tumor | Giant Cell Glioblastoma | Hashimoto Thyroiditis | Haim-Munk Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Alkaptonuria | Myelitis, Transverse | Pyruvate Kinase Deficiency | Mixed Connective Tissue Disease | Carey-Fineman-Ziter Syndrome | Hypolipoproteinemia | Ophthalmoplegia | Senior-Loken Syndrome | Pneumococcal Meningitis | Cole-Carpenter Syndrome | Congenital Aniridia | LEOPARD Syndrome | IMAGe Syndrome | Farber Disease | Chiari Malformation Type I | Gilbert Syndrome | Congenital Mirror Movements | Wolff-Parkinson-White Syndrome | Encephalitis | Epidermolysis Bullosa Dystrophica | Optic Neuropathy | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Arthritis, Psoriatic | Mast Cell Leukemia | Carcinoma, Transitional Cell | Protein S Deficiency | Lamellar Ichthyosis | Sotos Syndrome | Hyperbilirubinemia | Thyroid Dyshormonogenesis | Papulopustular Rosacea | Microphthalmia | Vogt-Koyanagi-Harada Syndrome | Sjogren Syndrome | Bladder Exstrophy | Retinal Degeneration | Coronary Artery Disease | Hyperhomocysteinemia | Lymphangioma | Melanoma, Uveal | Diabetes | Mannosidase Deficiency Diseases | Proopiomelanocortin Deficiency | Hypersensitivity Pneumonitis | Amelanotic Melanoma | Progressive Familial Intrahepatic Cholestasis Type 3 | Diabetic Neuropathy | Trichotillomania | Pneumonia, Bacterial | Anorectal Malformations | Lymphoma, Mantle Cell | Tinea | Progressive Familial Intrahepatic Cholestasis Type 1 | Gallstones | Steel Syndrome | Specific Granule Deficiency | Bullous Pemphigoid | Meningitis | Thrombocythemia, Essential | Familial Hypertrophic Cardiomyopathy | Nail Disorder, Nonsyndromic Congenital | Shprintzen-Goldberg Syndrome | Metatropic Dysplasia | Hyperparathyroidism | Leber Congenital Amaurosis | DICER1 Syndrome | Retinitis | Perry Syndrome | Renal Oncocytoma | Epidermolytic Ichthyosis, Annular | Palmoplantar Keratoderma | Pseudohermaphroditism | Fuchs Heterochromic Iridocyclitis | Chromosome 9q34.3 Deletion Syndrome | Phenylketonuria | Whipple's Disease | Osteogenesis Imperfecta Type I | Alpers Syndrome | Antenatal Bartter Syndrome Type 1 | Xeroderma Pigmentosum | Multifocal Motor Neuropathy | Congenital Bile Acid Synthesis Defect | Rolandic Epilepsy | Albinism | Pure Red Cell Aplasia | Vascular Cognitive Impairment | Hyperbilirubinemia, Neonatal | Goiter | Hemophagocytic Lymphohistiocytosis | Nasodigitoacoustic Syndrome | Sarcoma | Leukocyte Adhesion Deficiency | Progressive Myoclonic Epilepsy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Glioblastoma Multiforme | Patent Foramen Ovale | Acute Chest Syndrome | Sarcomatoid Carcinoma Of The Lung | Tendinopathy | Ectodermal Dysplasia | Angioimmunoblastic T-cell Lymphoma | Hypercholesterolemia, Familial | Inflammatory Myopathy | Spinocerebellar Ataxia Type 14 | Pulmonary Stenosis | Toxic Epidermal Necrolysis | Achondrogenesis | Cataract | Acromesomelic Dysplasia | Kabuki Syndrome | Congenital Fiber-type Disproportion Myopathy | Lassa Fever | Acquired Partial Lipodystrophy | Cerebellar Ataxia, Cayman Type | Cyclic Vomiting Syndrome | Retinal Dystrophy, Early-onset Severe | Intestinal Tuberculosis | Bartter Syndrome | Glucagonoma | Oguchi Disease-2 | Duane Retraction Syndrome | Polycystic Ovary Syndrome | Pseudomyxoma Peritonei | Anti-NMDA Receptor Encephalitis | Sleep Apnea, Obstructive | Leri-Weill Dyschondrosteosis | Glycogen Storage Disease Type 6 | Multiple Sclerosis, Secondary Progressive | Dysmorphophobia | Biotinidase Deficiency | Nephroblastoma | Cystitis, Interstitial | Persistent Fetal Circulation | Fukuyama Congenital Muscular Dystrophy | Rhizomelic Chondrodysplasia Punctata | Synpolydactyly | Renpenning Syndrome | Hypocalcemia | Homocystinuria | Snyder-Robinson Syndrome | Myofibromatosis | Lipid Metabolism Disorders | Keratoconjunctivitis | Noonan Syndrome | Epicondylitis | Gastroenteritis | Myotonic Disorders | Ulcerative Colitis | Marfan Syndrome | Keratosis, Actinic | Burn-McKeown Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Juvenile Myelomonocytic Leukemia | Multiple Sclerosis | Mesothelioma, Malignant | Colon Adenoma | Aldosteronism | Knobloch Syndrome | Pleomorphic Xanthoastrocytoma | Pierre Robin Syndrome | Rotor Syndrome | Epidermolysis Bullosa | Leishmaniasis, Visceral | Stiff-man Syndrome | Asthma | Hyperuricemia | Sensory Neuropathy | Partington Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Pneumonia, Viral | Hypercalcemia | Uremia | Hypervalinemia | Takenouchi-Kosaki Syndrome | Paraplegia | Borderline Personality Disorder | Loeys-Dietz Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Esophageal Adenocarcinoma | Hepatitis A | Impulse Control Disorder | Agammaglobulinemia | Cancer, Bladder | Cousin Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Peeling Skin Syndrome Type B | Hemochromatosis Type 2 | Gerstmann-Straussler-Scheinker Syndrome | Cannabis Abuse | Myasthenia | CHOPS Syndrome | Glycogen Storage Disease | Optic Neuropathy, Anterior Ischemic | Spondylocarpotarsal Synostosis Syndrome | Histiocytosis | Peyronie's Disease | Immunoproliferative Disorders | Ischemia | Communication Disorders | Camurati-Engelmann Disease | Chronic Granulomatous Disease, X-linked | Nutrition Disorders | Hypertension, Renal | Progressive Osseous Heteroplasia | Charcot-Marie-Tooth Disease, Type 1A | Pituitary Dwarfism | Craniopharyngioma | Nemaline Myopathy 10 | Cold Agglutinin Disease | Spasticity | Papillorenal Syndrome | Discoid Lupus Erythematosus | Sarcoma, Alveolar Soft Part | Chronic Beryllium Disease | Pierpont Syndrome | Bloom Syndrome