Cerebral Malaria

About the Disease
Malaria, also known as malaria, susceptibility to, is related to plasmodium falciparum malaria and plasmodium vivax malaria, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Malaria is SLC4A1 (Solute Carrier Family 4 Member 1 (Diego Blood Group)), and among its related pathways/superpathways are Innate Immune System and Response to elevated platelet cytosolic Ca2+. The drugs Lumefantrine and Artemether have been mentioned in the context of this disorder. Affiliated tissues include spleen, liver and t cells, and related phenotypes are nausea and vomiting and fever

Common Targets
STAT6 | IL17RA | IL4R | ABCA1 | G3569 | PROCR | Eukaryotic Translation Initiation Factor 4A (eIF-4A) | CR1 | HBB | IL4 | FCGR2A | RNASE3 | IFNAR1 | CXCL10 | G6PD | TLR7 | ABO | ATP2B4 | ART3 | CD40LG | LOC105372848

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Other Diseases

Porokeratosis | Acute Anterior Uveitis | Peroxisomal Disorder | Hypertension, Portal | Neurocutaneous Melanocytosis | Osteochondroma | Autoimmune Hemolytic Anemia | Neurofibromatosis | Smoldering Myeloma | Intermittent Claudication | Spinal Cord Diseases | Crimean-Congo Hemorrhagic Fever | Congenital Heart Block | Rubinstein-Taybi Syndrome | Seizures | Metachromatic Leukodystrophy | Analgesia | Early Infantile Epileptic Encephalopathy 4 | Metatropic Dysplasia | Herpes Genitalis | Endometritis | Gaucher Disease | Walker-Warburg Syndrome | Neuromyelitis Optica | Combined Malonic And Methylmalonic Acidemia | Hereditary Xerocytosis | Acrodermatitis Enteropathica | Hyperinsulinism-hyperammonemia Syndrome | Triple A Syndrome | Primary Lateral Sclerosis | Sick Sinus Syndrome 1 | Epidermolysis Bullosa Acquisita | Inflammatory Linear Verrucous Epidermal Nevus | Choroideremia | Trichomegaly | Hemochromatosis Type 2 | Bloom Syndrome | Familial Partial Lipodystrophy | Congenital Adrenal Hyperplasia | Glaucomatocyclitic Crisis | Dysfibrinogenemia | Congenital Generalized Lipodystrophy | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Porphyria, Acute Intermittent | Congenital Hypofibrinogenemia | Hypervalinemia | Hyperlipidemia, Familial Combined | Niemann-Pick Disease, Type A | Basal Ganglia Disease | Familial Thoracic Aortic Aneurysm | Proximal Symphalangism | Autoimmune Polyendocrine Syndrome | Nijmegen Breakage Syndrome | Benign Familial Pemphigus | Charcot-Marie-Tooth Disease, Type 1A | Spinocerebellar Ataxia Type 23 | Hydrocephalus, Normal Pressure | Proctitis | Meier-Gorlin Syndrome | Posterior Polar Cataract | Frank-ter Haar Syndrome | Dental Caries | Pouchitis | GM2-gangliosidosis AB Variant | Pulmonary Alveolar Microlithiasis | Reticular Dysgenesis | Congenital Tufting Enteropathy | Purpura, Thrombotic Thrombocytopenic | Distal Spinal Muscular Atrophy | Postaxial Polydactyly | Citrullinemia | Congenital Hereditary Endothelial Dystrophy Type I | Split Hand-foot Malformation | Autoimmune Polyendocrinopathy Syndrome Type I | Familial Isolated Hyperparathyroidism | Meningitis | N-acetylglutamate Synthase Deficiency | Renal Tubular Acidosis | Galactosemia | Pleural Tuberculosis | Hypertensive Nephropathy | Kashin-Beck Disease | DiGeorge Syndrome | Scleroderma, Diffuse | Anodontia | Fibromyalgia | Small Lymphocytic Lymphoma | Vitamin D Deficiency | Oligodendroglioma | Cystitis, Interstitial | Uremic Pruritus | Neuromyotonia | Tylosis With Esophageal Cancer | Pierson Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Neuropathy | Cryopyrin-associated Periodic Syndromes | Pregnancy, Ectopic | Medulloblastoma | Lymphoma, Follicular | Prader-Willi Syndrome | Familial Exudative Vitreoretinopathy | Pre-eclampsia | Neurodevelopmental Disorders | Achondrogenesis | Glycogen Storage Disease Type 6 | Rheumatic Heart Disease | Mitochondrial Encephalomyopathy | Coronary Restenosis | Long QT Syndrome Type 1 | Hepatoblastoma | Mucolipidosis Type II | Premenstrual Syndrome | Sulfite Oxidase Deficiency | Proopiomelanocortin Deficiency | Nephrosclerosis | Hyperthermia, Malignant | Feingold Syndrome | Intellectual Disability, Autosomal Dominant 5 | Farber Disease | Inflammatory Bowel Disease | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Leukemia-lymphoma, Adult T-cell | Adenylosuccinate Lyase Deficiency | Neurofibromatosis-Noonan Syndrome | Myosin Storage Myopathy | Chronic Beryllium Disease | Persistent Fetal Circulation | Insulinoma | Prolactinoma | Anthrax | Chudley-McCullough Syndrome | Graft-versus-host Disease | Congenital Torticollis | Gangliosidosis, GM1 | Kohlschutter-Tonz Syndrome | Arteriovenous Malformations | CREST Syndrome | Agoraphobia | Pancreatitis | MIRAGE Syndrome | Carney-Stratakis Syndrome | Pulverulent Zonular Cataract | Myeloid Leukemia | Osteochondrosis | Guanidinoacetate Methyltransferase Deficiency | Still Disease | Birt-Hogg-Dube Syndrome | Wieacker-Wolff Syndrome | Cole-Carpenter Syndrome | Meningioma, Benign | Hypothyroidism | Chronic Myeloid Leukemia | Milk Allergy | Nephrotic Syndrome | Mannosidase Deficiency Diseases | Treacher Collins Syndrome | Narcolepsy | Inflammatory Myofibroblastic Tumor | Iron Overload | Acute Chest Syndrome | Myocardial Infarction | Angiosarcoma | Polycystic Kidney, Autosomal Dominant | Sandhoff Disease | Epiphyseal Chondrodysplasia, Miura Type | Chitayat Syndrome | Alkaptonuria | Hepatitis E | Bethlem Myopathy | Multiple Myeloma | Postpartum Depression | Intestinal Pseudo-obstruction | 3-methylglutaconic Aciduria | Pelizaeus-Merzbacher Disease | Carpenter Syndrome | Vitiligo | Chronic Idiopathic Myelofibrosis | Pitt-Hopkins Syndrome | Progressive Familial Intrahepatic Cholestasis | Bardet-Biedl Syndrome | Eczema | Hereditary Sensory And Autonomic Neuropathy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Multiple Sulfatase Deficiency | Acne | Eccrine Porocarcinoma | Brooke-Spiegler Syndrome | Hyperhomocysteinemia | Corneal Dystrophy And Perceptive Deafness | Coronary Artery Disease | Heterotaxy | Hypogammaglobulinemia | Metabolic Diseases | Craniosynostosis | Renal Oncocytoma | Charcot-Marie-Tooth Disease, Type 2A | Gastritis, Atrophic | Esophageal Adenocarcinoma | Papillorenal Syndrome | Lipid Storage Myopathy | Charcot-Marie-Tooth Disease Axonal Type 2N | Membranous Nephropathy | Cornelia De Lange Syndrome | Common Variable Immunodeficiency | Ependymoma | Fundus Albipunctatus | Osteogenesis Imperfecta | Peripheral T-cell Lymphoma | Familial Hemiplegic Migraine | Cohen Syndrome | Low Tension Glaucoma | Nephrocalcinosis | Cerebellofaciodental Syndrome | Limb Girdle Muscular Dystrophy | Bartter Syndrome | Dementia, Vascular | Ichthyosis | Allergic Contact Dermatitis | Demyelinating Diseases | Skin Fragility-woolly Hair Syndrome | Spinocerebellar Ataxia Type 13 | Spinocerebellar Ataxia Type 40 | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Periventricular Nodular Heterotopia | Bietti Crystalline Dystrophy | Congenital Afibrinogenemia | McCune-Albright Syndrome | Asplenia | Vitamin K Deficiency | Personality Disorders | Addison Disease | Disseminated Intravascular Coagulation | Babesiosis | Goldenhar Syndrome | Fahr Disease | Retinoschisis | Viral Meningitis | Early Infantile Epileptic Encephalopathy 1 | Lamellar Ichthyosis | Chorioretinitis | Aldosterone Synthase Deficiency | Uremia | Aneurysm, Thoracic Aortic | Tardive Dyskinesia | Glioma | Crohn's Disease | Echinococcosis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Polyarteritis Nodosa | Pyoderma Gangrenosum | Myhre Syndrome | Glomerulonephritis | Hypobetalipoproteinemias | Pleomorphic Xanthoastrocytoma | Shprintzen-Goldberg Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Snyder-Robinson Syndrome | Enlarged Vestibular Aqueduct | Liver Failure, Acute Infantile | Osteitis | Peeling Skin Syndrome, Acral Type | Headache | Lymphoma | Nephritis, Interstitial | Toxic Epidermal Necrolysis | Osteonecrosis | Lymphoma, B-cell | Smith-Lemli-Opitz Syndrome | Benign Recurrent Intrahepatic Cholestasis 1 | Hartsfield Syndrome | Alopecia | Batten Disease | Chediak-Higashi Syndrome | Hemolytic Anemia | Bronchiolitis | Guttate Psoriasis | Desbuquois Syndrome | Acne Vulgaris | Spinocerebellar Ataxia Type 6 | Congenital Primary Aphakia | Pycnodysostosis | Hypopituitarism | Thrombosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Cardiac Sarcoidosis | 3C Syndrome | Imerslund-Grasbeck Syndrome | Gastric Atrophy | Motion Sickness | Mitochondrial Myopathy | Hypopigmentation | Prolymphocytic Leukemia | Hypertension, Renovascular | Polyradiculopathy | Agranulocytosis | Hypercholesterolemia | Waardenburg Syndrome Type 2A | Camurati-Engelmann Disease | Neuromuscular Disorders | Splenomegaly | Chondrosarcoma | Muscle Wasting | Kaposiform Hemangioendothelioma | Relapsing Polychondritis | Arthropathy | Glycogen Storage Disease Type 4 | Stevens-Johnson Syndrome | Pyelonephritis | Heterotopic Ossification | Spinocerebellar Ataxia Type 2 | Cysticercosis | Microcephalic Primordial Dwarfism | Glycogen Storage Disease Type 1 | Histiocytic Sarcoma | Schizoaffective Disorder | Paraganglioma, Carotid Body | Adenomyosis | Hyperprolactinemia | Tricho-hepato-enteric Syndrome | Histoplasmosis | Wolfram Syndrome | Osteosarcoma | Ganglioneuroma | DOCK8 Immunodeficiency Syndrome | Amyloidosis | Myotonia | Hyperparathyroidism | Plasma Cell Leukemia | Vestibular Disease | Juvenile Myelomonocytic Leukemia | Osteosclerosis | Cutaneous Angiosarcoma | Malaria, Cerebral | Oligoastrocytoma | Multiple Sclerosis, Secondary Progressive | Arthritis, Reactive | Dowling-Degos Disease | Motor Neuron Diseases | Brenner Tumor | Epidermolysis Bullosa Simplex | Osteopathia Striata With Cranial Sclerosis | Yellow Fever | Congenital Disorders Of Glycosylation | Miyoshi Myopathy | Papilloma | X-linked Creatine Transporter Deficiency | Orthostatic Intolerance | Keratitis-ichthyosis-deafness Syndrome | Presbyopia | Esophagitis, Eosinophilic | Diabetic Macular Edema | Focal Dermal Hypoplasia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Niemann-Pick Disease, Type B | Crigler-Najjar Syndrome | Smith-Magenis Syndrome | Sitosterolemia | Epilepsy Of Infancy With Migrating Focal Seizures | Carotid Artery Disease | Blue Nevus | Tyrosinemia Type 1 | Porphyria Cutanea Tarda | Gnathodiaphyseal Dysplasia | Osteomyelitis | Spinocerebellar Ataxia | Cholestasis, Intrahepatic | Dysequilibrium Syndrome | Sclerosteosis | Familial Advanced Sleep Phase Syndrome | Esthesioneuroblastoma | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Carcinoma, Signet Ring Cell | LEOPARD Syndrome | Vulvovaginitis | Epidermolytic Palmoplantar Keratoderma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Greig Cephalopolysyndactyly Syndrome | Early Infantile Epileptic Encephalopathy 28 | Exfoliative Dermatitis | Lupus Erythematosus | Hereditary Spherocytosis | Blastoma, Pleuropulmonary | Amelogenesis Imperfecta | Adrenal Insufficiency | Spinocerebellar Ataxia Type 15 | Periodontitis | Wagner Disease | Homocystinuria | Cheilitis | Influenza | Hydronephrosis | Parapsoriasis | Coloboma | Amebiasis | Lymphomatoid Granulomatosis | Schaaf-Yang Syndrome | Cold Agglutinin Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Mevalonate Kinase Deficiency