Disease

Meningitis

About the Disease
Meningitis, also known as fungal meningitis due to cryptococcus neoformans, is related to meningococcal meningitis and tuberculous meningitis, and has symptoms including back pain, fever and headache. An important gene associated with Meningitis is CRP (C-Reactive Protein), and among its related pathways/superpathways are ERK Signaling and Innate Immune System. The drugs Phenytoin and Acetaminophen have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and bone marrow, and related phenotypes are no effect and no effect

Common Targets
PTPN6 | PROC | IL10 | G3576 | G1956 | G7124 | G3569 | Opioid receptor (nonspecified subtype) | ARG1 | Cysteine Protease (nonspecified subtype) | OPRD1 | GPR17

疾病靶点研报
Meningitis

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

Other Diseases

Schindler Disease | Congenital Adrenal Hyperplasia 1 | Graft-versus-host Disease | Greig Cephalopolysyndactyly Syndrome | Erythema Multiforme | Polyradiculopathy | Nephrosclerosis | Familial Hypobetalipoproteinemia | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Agnathia-Otocephaly Complex | Epidermolysis Bullosa Simplex | Thymoma, Malignant | Common Cold | IgA Deficiency | Analgesia | Deafness, Dystonia, And Cerebral Hypomyelination | Glucagonoma | ICF Syndrome | Myasthenia | IgA Nephropathy | Lymphopenia | Osteogenesis Imperfecta Type I | Hypertension | Marfan Syndrome | Jaundice, Obstructive | Gastroschisis | Cardiac Sarcoidosis | Hypotonia-cystinuria Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Stroke, Hemorrhagic | Colitis, Collagenous | Lyme Disease | Psoriasis | Adrenal Insufficiency | Tyrosine Hydroxylase Deficiency | Congenital Disorders Of Glycosylation Type II | Acute Kidney Injury | Retinoschisis | Prostatitis | Isovaleric Acidemia | Sweet Syndrome | Pycnodysostosis | McCune-Albright Syndrome | Argininosuccinic Aciduria | Fibrillation, Atrial | Sarcoidosis, Pulmonary | Sensory Neuropathy | Subacute Sclerosing Panencephalitis | Acromesomelic Dysplasia | Fuchs Dystrophy | Wolfram Syndrome 2 | Anencephaly | Myelitis, Transverse | Beta-Propeller Protein-associated Neurodegeneration | Gliosarcoma | Superficial Spreading Melanoma | Acromicric Dysplasia | Non-epidermolytic Palmoplantar Keratoderma | Myocarditis | Osteogenesis Imperfecta Type III | Cancer, Skin | Large Granular Lymphocytic Leukemia | Spinocerebellar Ataxia Type 23 | Chediak-Higashi Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Skin Fragility-woolly Hair Syndrome | Dementia | Spondylocostal Dysostosis | Autoimmune Disease | Ocular Albinism Type 1 | Multicentric Carpotarsal Osteolysis Syndrome | Essential Fructosuria | Vertebrobasilar Insufficiency | Acrocallosal Syndrome | Photosensitivity | Rothmund-Thomson Syndrome | Hyperekplexia | Nager Acrofacial Dysostosis | Scoliosis | Patent Foramen Ovale | Schamberg Disease | Canavan Disease | Hypertensive Retinopathy | Carcinoma In Situ | Muckle-Wells Syndrome | Paracoccidioidomycosis | Graves Disease | Progressive Osseous Heteroplasia | GATA2 Deficiency | Polycythemia Vera | Neuroma | Diabetes Insipidus, Nephrogenic | Lipodystrophy | Strabismus | Porphyria, Acute Intermittent | Prune Belly Syndrome | Supravalvular Aortic Stenosis | Ebstein Anomaly | Basal Ganglia Disease | Amelanotic Melanoma | Papillon-Lefevre Syndrome | Syncope | Ischemia | Adenomyosis | Schizoaffective Disorder | Congenital Hemolytic Anemia | Herpes Genitalis | Urethritis | Seasonal Mood Disorder | Generalized Epilepsy With Febrile Seizures Plus | Pelizaeus-Merzbacher Disease | Disseminated Intravascular Coagulation | Rhabdomyosarcoma, Embryonal | Carcinoma, Signet Ring Cell | Iron Metabolism Disorders | Microtia | Dysequilibrium Syndrome | Chromosome 5q Deletion Syndrome | Waardenburg Syndrome Type 4A | Adenomatoid Tumor | Migraine | Creatine Deficiency Syndrome | Dengue Hemorrhagic Fever | Dyslipidemia | Hypophosphatasia | Retinal Coloboma | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Seminoma | Glanzmann Thrombasthenia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | C3 Glomerulonephritis | Cholestasis, Intrahepatic | Anal Fissure | Congenital Dyserythropoietic Anemia | WAGR Syndrome | Thrombasthenia | Angioedema | Scapuloperoneal Spinal Muscular Atrophy | Cardiomyopathy, Hypertrophic | Keratosis | Schizophrenia | Epidermolysis Bullosa | Hyperoxaluria | Ectopia Lentis, Isolated, Autosomal Recessive | Tularemia | HIBCH Deficiency | Bone Giant Cell Tumor | Hyperprolactinemia | Myelodysplasia | Alzheimer Disease, Late Onset | Hyperacusis | Waardenburg Syndrome Type 2 | Amenorrhea | Intestinal Hypomagnesemia 1 | Immunoproliferative Disorders | Nephronophthisis | Early Infantile Epileptic Encephalopathy 4 | Eosinophilic Asthma | Pyruvate Carboxylase Deficiency Disease | Cryoglobulinemia | Bartsocas-Papas Syndrome | Autoimmune Hemolytic Anemia | Autonomic Neuropathy | Tinea Versicolor | Glutathione Synthetase Deficiency | Palsy, Cerebral | Pyruvate Dehydrogenase Deficiency | Silicosis | Glycogen Storage Disease Type 1a | Urolithiasis | Phenylketonuria | Budd-Chiari Syndrome | Limb Girdle Muscular Dystrophy | Hairy Cell Leukemia | Craniofacial Dysostosis | Insulinoma | Polydactyly | Huntington's Disease | Acquired Partial Lipodystrophy | Neuroectodermal Tumors, Primitive | Best Macular Dystrophy | Intellectual Disability, Autosomal Dominant 5 | Kidney Stones | Early Infantile Epileptic Encephalopathy 13 | Learning Disability | Mucolipidosis | Sezary Syndrome | Multiple Sclerosis, Secondary Progressive | Arthritis, Psoriatic | Carbonic Anhydrase VA Deficiency | Vasculitis | Corneal Dystrophies, Hereditary | Pure Red Cell Aplasia | Major Depression | Malaria, Cerebral | Hepatorenal Syndrome | Multiple Sclerosis, Relapsing-remitting | Mucolipidosis Type III | Rotor Syndrome | Trichomegaly | Glycogen Storage Disease Type 3 | Pyruvate Kinase Deficiency | GAPO Syndrome | Oculopharyngeal Muscular Dystrophy | Meningioma, Benign | Hypokalemia | Incontinentia Pigmenti | Crouzon Syndrome With Acanthosis Nigricans | Neuropathy | Birt-Hogg-Dube Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Micro Syndrome | Splenomegaly | Asperger Syndrome | Bullous Pemphigoid | Premature Ejaculation | Carcinoma, Merkel Cell | Urticaria | Hemimegalencephaly | Progressive Myoclonic Epilepsy | NGLY1 Deficiency | Juvenile Myelomonocytic Leukemia | Leishmaniasis, Visceral | Salla Disease | Mohr-Tranebjaerg Syndrome | Blue Rubber Bleb Nevus Syndrome | Arthritis | Senior-Loken Syndrome | Primary Lateral Sclerosis | Cutaneous T-cell Lymphoma | Stargardt Disease | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Fahr Disease | Myositis, Focal | Epidermolytic Palmoplantar Keratoderma | Fanconi Anemia | Porokeratosis | Burn-McKeown Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Carney-Stratakis Syndrome | Ependymoma | Neuromyelitis Optica | Myoclonic Epilepsy With Ragged Red Fibers | Calcium Pyrophosphate Deposition Disease | Dystonia-parkinsonism, X-linked | Glaucoma | Riboflavin Transporter Deficiency Neuronopathy | Congenital Stationary Night Blindness | Becker Muscular Dystrophy | Non-proliferative Diabetic Retinopathy | Personality Disorders | Corneal Dystrophy | Charcot-Marie-Tooth Disease Axonal Type 2N | Takenouchi-Kosaki Syndrome | Woodhouse-Sakati Syndrome | Vitamin B12 Deficiency | Congenital Mirror Movements | Cataplexy | Diabetic Encephalopathy | Tumoral Calcinosis | Iron Deficiency Anemia | Sengers Syndrome | Blepharitis | Cantu Syndrome | Schizencephaly | Alopecia Totalis | Arthritis, Gouty | 5-oxoprolinase Deficiency | Spasticity | Charcot-Marie-Tooth Disease Type 3 | Netherton Syndrome | Syphilis | Asthma | Glycogen Storage Disease Type 5 | Polycythemia | Agranulocytosis | Gastroenteritis | Hyperinsulinemia | Tay-Sachs Disease | Temporal Lobe Epilepsy | Enlarged Vestibular Aqueduct | Leukodystrophies | Macrophage Activation Syndrome | Adenylosuccinate Lyase Deficiency | Acute Chest Syndrome | Basan Syndrome | Infectious Diarrhea | Dystonia | Hydrocephalus, Normal Pressure | Vitreoretinopathy, Proliferative | Basal Ganglia Cerebrovascular Disease | Carpal Tunnel Syndrome | Creutzfeldt-Jakob Disease | Pancreatitis | Spinocerebellar Ataxia Type 40 | Williams Syndrome | Hyperlipidemia, Familial Combined | Cholesteryl Ester Storage Disease | Chronic Inflammatory Demyelinating Polyneuropathy | Metanephric Adenoma | Brenner Tumor | Pure Autonomic Failure | Chronic Idiopathic Myelofibrosis | Aplastic Anemia | Synpolydactyly | Cataract | Bronchiectasis | Encephalitis | Spinal Muscular Atrophy Type 2 | Primrose Syndrome | Astigmatism | Infantile Liver Failure Syndrome 1 | Aphasia | VACTERL Association | FG Syndrome | Gitelman Syndrome | Oligoasthenoteratozoospermia | Oguchi Disease-2 | Bernard-Soulier Syndrome | Hyperlipidemia Type V | Arthrogryposis | Pneumonia, Bacterial | Neurogenic Bladder | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Intracerebral Hemorrhage | Scleritis | Acne Vulgaris | Anti-NMDA Receptor Encephalitis | Uveitis | Hypersensitivity Pneumonitis | Lung Diseases | Birk-Barel Syndrome | Chorea | Hamartoma | Seborrheic Dermatitis | Intermittent Claudication | Rubinstein-Taybi Syndrome | Inflammatory Joint Disease | Cryptosporidiosis | Congenital Adrenal Hyperplasia | Pseudohermaphroditism | Rhabdomyosarcoma, Alveolar | Farber Disease | Hemangioendothelioma | Congenital Heart Defects | Paronychia | Liver Failure, Acute Infantile | Multicystic Renal Dysplasia | Localized Scleroderma | Interstitial Lung Diseases | Gangliosidosis | Esophagitis | Toxoplasmosis | Pyruvate Decarboxylase Deficiency | Epithelial-myoepithelial Carcinoma | DiGeorge Syndrome | Lipid Metabolism Disorders | Myelomeningocele | Megaloblastic Anemia | Holt-Oram Syndrome | Cardiospondylocarpofacial Syndrome | Chronic Myeloid Leukemia | Melnick-Needles Syndrome | Retinal Telangiectasia | Oculocutaneous Albinism | Occipital Neuralgia | Pancreatitis, Chronic | Esophageal Motility Disorders | Hepatic Adenomatosis | Cavitary Optic Disc Anomalies | Cancer, Prostate | Meningioma | Congenital Heart Block | Hereditary Mixed Polyposis Syndrome | Focal Facial Dermal Dysplasia | Dysfibrinogenemia | Myeloid Leukemia | Aneurysm, Thoracic Aortic | Hyperbilirubinemia, Neonatal | Cutis Laxa | Trichotillomania | Mitochondrial Myopathy | Hypohidrotic Ectodermal Dysplasia, X-linked | Insulin Resistance | Orotic Aciduria | Vulvovaginitis | L-2-Hydroxyglutaric Aciduria | Gestational Trophoblastic Disease | Arterial Tortuosity Syndrome | Erectile Dysfunction | Antenatal Bartter Syndrome Type 1 | Blepharo-cheilo-odontic Syndrome | Gerodermia Osteodysplastica | Fucosidosis | Genitopatellar Syndrome | Crimean-Congo Hemorrhagic Fever | Long QT Syndrome Type 3 | Usher Syndrome Type III | Optic Neuropathy, Anterior Ischemic | Congenital Aniridia