Disease

Bacterial Meningitis

About the Disease
Bacterial Meningitis, also known as meningitis, bacterial, is related to meningococcal meningitis and aseptic meningitis. An important gene associated with Bacterial Meningitis is CRP (C-Reactive Protein), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Acetaminophen and Cefotaxime have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and cortex, and related phenotypes are no effect and no effect

Common Targets
ELL2 | SERPINC1 | CPB2 | PLAT | PROZ | MBL2 | SERPINA5 | TLR2 | ADRB2 | THBD | LTA4H | DPEP1

疾病靶点研报
Bacterial Meningitis

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

Other Diseases

Chondrodysplasia Punctata 2, X-linked Dominant | Cholecystitis | Galactosialidosis | Angiosarcoma Of The Breast | Papilledema | Cholesteryl Ester Storage Disease | Hyperprolactinemia | Meningioma, Benign | Epicondylitis | Lymphoma, B-cell | Hermansky-Pudlak Syndrome | Conjunctivitis, Allergic | Proctitis | Dwarfism | Glaucomatocyclitic Crisis | Cholestasis | Glomerulonephritis, Membranous | Asphyxia Neonatorum | Restrictive Dermopathy | Inflammatory Bowel Disease | Hepatitis C, Chronic | Poikiloderma With Neutropenia | Globozoospermia | Leigh Syndrome | Polyarteritis Nodosa | B-cell Chronic Lymphocytic Leukemia | Diamond-Blackfan Anemia | Encephalitis, Tick-borne | Histiocytosis | Myeloid Leukemia | Antley-Bixler Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Central Core Disease | Optic Nerve Diseases | Neurofibrosarcoma | Osteomyelitis | Craniometaphyseal Dysplasia | Nicotine Dependence | Aplasia Cutis Congenita | Allergic Contact Dermatitis | Eclampsia | Hypertension, Renal | Pancreatitis, Chronic | Pleomorphic Xanthoastrocytoma | Vici Syndrome | Angiodysplasia | Congenital Myasthenic Syndrome | Ghosal Syndrome | Syphilis | Leukocyte Adhesion Deficiency | Strabismus | Angioedema, Acquired | Pyoderma Gangrenosum | Mitochondrial Disease | Hemophilia | Cataract | Lymphangioma | Schizoaffective Disorder | Synpolydactyly | Microphthalmia, Syndromic 7 | Hyperacusis | Restless Legs Syndrome | Corneal Neovascularization | Dementia | Ovarian Hyperstimulation Syndrome | Acrocallosal Syndrome | Focal Facial Dermal Dysplasia | Myosin Storage Myopathy | Cholelithiasis | Herpes Genitalis | Neuroblastoma | Osteochondroma | Patent Foramen Ovale | Tenosynovial Giant Cell Tumor | Myopia | Hypertensive Retinopathy | Osteogenesis Imperfecta | Nutrition Disorders | Multicystic Renal Dysplasia | Hypohidrotic Ectodermal Dysplasia, X-linked | Esophageal Adenocarcinoma | Hypersensitivity Pneumonitis | Peters-plus Syndrome | Autonomic Nervous System Disorders | Keratoacanthoma | Infantile Spasm | Charcot-Marie-Tooth Disease Type 2T | Hepatitis E | Schizophrenia, Paranoid | Wolman Disease | Adams-Oliver Syndrome | Myelitis, Transverse | Sporadic Hemiplegic Migraine | Mannosidase Deficiency Diseases | Iron Metabolism Disorders | Anthrax | Vascular Cognitive Impairment | Antisocial Personality Disorder | Oguchi Disease-2 | Sarcoidosis | Pulmonary Tuberculosis | WAGR Syndrome | ADNP Syndrome | DICER1 Syndrome | Marfan Syndrome | Methemoglobinemia | Neuroendocrine Cancer | N-acetylglutamate Synthase Deficiency | Benign Hereditary Chorea | Alkaptonuria | Sarcoma, Endometrial Stromal | Pierson Syndrome | Keloid | Conduct Disorder | Holoprosencephaly | Hepatitis, Chronic | Cenani-Lenz Syndactyly Syndrome | Mitochondrial Encephalomyopathy | Pneumoconiosis | Spinocerebellar Ataxia | Senior-Loken Syndrome | Malaria | Giant Cell Glioblastoma | Trichuriasis | Argininosuccinic Aciduria | Leukemia | Hepatitis | Prurigo Nodularis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Blastoma, Pleuropulmonary | Tyrosinemia Type 1 | Hemangioblastoma | Uveitis | Spinal Muscular Atrophy Type 2 | Schwannoma | Netherton Syndrome | Hydrolethalus Syndrome | Mucolipidosis | Anal Fissure | Myositis, Focal | Spinocerebellar Ataxia Type 13 | Cardiospondylocarpofacial Syndrome | Osteogenesis Imperfecta Type II | Mandibuloacral Dysplasia With Type A Lipodystrophy | Polycystic Liver | DNA Ligase IV Deficiency | Hyperbilirubinemia, Neonatal | Periventricular Nodular Heterotopia | Varicocele | Arts Syndrome | Non-proliferative Diabetic Retinopathy | Presbyopia | Osteoporosis-pseudoglioma Syndrome | Peritonitis | Sarcoma, Ewing | Oral Lichen Planus | Primary Hyperoxaluria Type 3 | Tetraplegia | Congenital Nystagmus | Moyamoya Disease | Intracerebral Hemorrhage | Otitis Externa | Ichthyosis | Autosomal Recessive Congenital Ichthyosis | Schamberg Disease | Cyst | Retinal Telangiectasia | Cerebellar Ataxia, Cayman Type | Rosacea | Diabetes Mellitus, Transient Neonatal | Meningioma | Porphyria, Acute Intermittent | Panic Disorder | Cerebrovascular Disorders | Aneurysm, Abdominal Aortic | Liver Failure | Prader-Willi Syndrome | Infectious Diarrhea | Hodgkin Lymphoma | Anemia | T-cell Chronic Lymphocytic Leukemia | Retinoschisis | Spinocerebellar Ataxia Type 21 | Preaxial Polydactyly | Lateral Meningocele Syndrome | AIDS Dementia Complex | Epidermal Nevus Syndrome | Cerebellofaciodental Syndrome | Giant Axonal Neuropathy | Necrotizing Autoimmune Myopathy | Vitamin K Deficiency | Chromosome 5q Deletion Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Pitt-Hopkins Syndrome | GNE Myopathy | Coma | Phenylketonuria II | Carcinoma, Small Cell | Retinal Vasculitis | Primary Pigmented Nodular Adrenocortical Disease | Mastitis | Congenital Tufting Enteropathy | Non-Hodgkin Lymphoma | Focal Dermal Hypoplasia | Odonto-onycho-dermal Dysplasia | Thrombosis | Avian Influenza | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Acrodermatitis | Charcot-Marie-Tooth Disease Axonal Type 2N | Left Ventricular Noncompaction | Hartnup Disease | Pemphigus Vulgaris | Kawasaki Disease | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Pituitary Stalk Interruption Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Eczema | Absence Epilepsy | Arthropathy | Rheumatic Heart Disease | Opisthorchiasis | Congenital Dyserythropoietic Anemia Type 1 | Neurofibromatosis | Lipodystrophy | Acanthosis Nigricans | Progressive Familial Intrahepatic Cholestasis Type 3 | Carotid Artery Disease | Neuroleptic Malignant Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Gastrointestinal Disorders | Prolymphocytic Leukemia | Leukodystrophies | Spinocerebellar Ataxia Type 8 | Obesity | Multiple Sclerosis | Glycogen Storage Disease Type 1b | Tendinopathy | Alpers Syndrome | Fibromuscular Dysplasia | Aldosterone Synthase Deficiency | Campomelic Dysplasia | Guillain-Barre Syndrome | Congenital Diaphragmatic Hernia | Epidermolysis Bullosa | Keratoconjunctivitis | Neurofibromatosis-Noonan Syndrome | Donnai-Barrow Syndrome | Pseudo-pseudohypoparathyroidism | Spinocerebellar Ataxia Type 15 | Myofibrillar Myopathy | Familial Cerebral Amyloid Angiopathy | Fibrillation, Atrial | Lichen Planus | LEOPARD Syndrome | Ocular Surface Squamous Neoplasia | CEDNIK Syndrome | Varices | Allan-Herndon-Dudley Syndrome | Intermittent Explosive Disorder | Papilloma | Aromatic L-amino Acid Decarboxylase Deficiency | Sandhoff Disease | Congenital Disorders Of Glycosylation | Pernicious Anemia | Peroxisomal Disorder | Encephalopathy, Glycine | Spitzoid Melanoma | Early Infantile Epileptic Encephalopathy | Agoraphobia | Hyperinsulinemia | Chromosome 16p11.2 Deletion Syndrome | Chloridorrhea, Congenital | Progressive Encephalopathy-optic Atrophy Syndrome | Borjeson-Forssman-Lehmann Syndrome | Malnutrition | Common Variable Immunodeficiency | Meningococcal Infections | Paracoccidioidomycosis | Progressive Familial Intrahepatic Cholestasis Type 1 | Osteogenesis Imperfecta Type I | Periodontitis | Adenocarcinoma | Hyperlipidemia Type V | Smoldering Myeloma | Fascioliasis | Trigonocephaly | Cavitary Optic Disc Anomalies | Cervical Dystonia | Ileitis | Ichthyosis Bullosa Of Siemens | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Cole-Carpenter Syndrome | Esophagitis, Eosinophilic | Chronic Neutrophilic Leukemia | Vitamin D Deficiency | Ulcerative Colitis | Trichotillomania | Hypertension, Pulmonary | Chronic Enteropathy Associated With SLCO2A1 Gene | Zellweger Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Cholangitis | Congenital Absence Of Vas Deferens | Placenta Previa | Dysequilibrium Syndrome | Choroiditis | Werner's Syndrome | Alpha-1 Antitrypsin Deficiency | Osteomalacia | X-linked Creatine Transporter Deficiency | Hydrocephalus, Normal Pressure | Coffin-Siris Syndrome | Measles | Neurofibromatosis Type 2 | L-2-Hydroxyglutaric Aciduria | Hemochromatosis | Inflammatory Myofibroblastic Tumor | Stomatitis | Methylmalonic Acidemia | Hypothyroidism | Herpes Simplex Dermatitis | Sialidosis Type I | Trichothiodystrophy | Seizures-scoliosis-macrocephaly Syndrome | GAPO Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Diffuse Palmoplantar Keratoderma | Tinea | IgA Nephropathy | Uremic Pruritus | Lamellar Ichthyosis | Constipation | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Hereditary Elliptocytosis | Alopecia Areata | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Cancer, Skin | McLeod Syndrome | Hereditary Spastic Paraplegia | Tietze Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Huntington's Disease | Peripheral T-cell Lymphoma | Salla Disease | Hereditary Inclusion Body Myopathy | Vasculitis | Esophagitis | Gout | Multiple Myeloma | Lymphoma Lymphoblastic | Small Lymphocytic Lymphoma | Fowler's Syndrome | Larsen Syndrome | Meniere's Disease | Hypophosphatemic Rickets, Autosomal Recessive, 1 | VEXAS Syndrome | Eosinophilic Asthma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Steel Syndrome | Glycogen Storage Disease | Congenital Adrenal Hyperplasia | Pancytopenia | Richter's Syndrome | Encephalopathy | Lipid Storage Myopathy | Fuchs Dystrophy | Hereditary Neuropathy With Liability To Pressure Palsies | Oculocutaneous Albinism Type 1 | Stevens-Johnson Syndrome | Porencephaly | Paroxysmal Nocturnal Hemoglobinuria | Schnitzler Syndrome | Hemochromatosis Type 2 | Oculocutaneous Albinism Type 4 | Dermatofibrosarcoma | Babesiosis | Carcinoid Tumor | Fahr Disease | Dysgerminoma | Pneumonia, Viral | Epidermolytic Palmoplantar Keratoderma | Urticaria | Hepatopulmonary Syndrome | Familial Isolated Hyperparathyroidism | Cartilage Disorders | Cholestasis, Intrahepatic | Intellectual Disability, Autosomal Dominant 5 | Chronic Lymphocytic Leukemia | Chordoma | Tremor | Cutaneous Angiosarcoma | Guttate Psoriasis | Sialidosis | Esophageal Carcinoma | Myhre Syndrome | Rotor Syndrome | Neovascular Glaucoma | Optic Nerve Hypoplasia, Bilateral