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

Hypotension, Orthostatic | Nephronophthisis | Familial Dysautonomia | Usher Syndrome Type II | Spinocerebellar Ataxia Type 40 | Paroxysmal Kinesigenic Dyskinesia | Intestinal Obstruction | Rhabdomyosarcoma, Alveolar | Spondyloperipheral Dysplasia | Neurodevelopmental Disorders | Hyperbilirubinemia | Peutz-Jeghers Syndrome | Diffuse Mesangial Sclerosis | Pericarditis | Central Core Disease | Melanoma, Uveal | Familial Exudative Vitreoretinopathy | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hemangioendothelioma | Melanoma | Fragile X Syndrome | Peyronie's Disease | Parkinson's Disease | C3 Glomerulonephritis | Stroke, Hemorrhagic | Lipodystrophy | Infertility, Male | Juvenile Xanthogranuloma | Polycythemia | Hereditary Inclusion Body Myopathy | Sarcoma, Endometrial Stromal | Cheilitis | Mitochondrial Encephalomyopathy | Treacher Collins Syndrome | Macular Corneal Dystrophy Type 1 | Salla Disease | Multiple Sclerosis, Primary Progressive | Usher Syndrome Type III | Pneumonia, Viral | Neurofibromatosis Type 2 | Hypercalcemia | Emery-Dreifuss Muscular Dystrophy | Danon Disease | Spinocerebellar Ataxia Type 21 | Robinow Syndrome | Glycogen Storage Disease Type 5 | Johanson-Blizzard Syndrome | Cholangitis | Seizures | Absence Epilepsy | Lymphomatoid Granulomatosis | Hartsfield Syndrome | Tibial Muscular Dystrophy | Meningitis | Triple A Syndrome | Usher Syndrome | Congenital Disorders Of Glycosylation | Okihiro Syndrome | Herpes Genitalis | N-acetylglutamate Synthase Deficiency | Atelosteogenesis Type 2 | Hyperlipidemia | Pulverulent Zonular Cataract | Chondrodysplasia Punctata 2, X-linked Dominant | Mitochondrial Cytopathy | Hypothalamic Obesity | Orthostatic Intolerance | Split Hand-foot Malformation | Chordoma | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Sotos Syndrome | Amblyopia | Eating Disorder | Glycogen Storage Disease Type 3 | Giant Cell Glioblastoma | Gyrate Atrophy Of The Choroid And Retina | Neurofibrosarcoma | Fucosidosis | Cholecystitis | Agranulocytosis | Chronic Myelomonocytic Leukemia | Usher Syndrome Type IIC | Spinocerebellar Ataxia Type 13 | Spinal Muscular Atrophy Type 3 | Schwannoma | Encephalopathy, Ethylmalonic | Tangier Disease | Spinocerebellar Ataxia Type 20 | Lassa Fever | Reye Syndrome | Ellis-Van Creveld Syndrome | Wilson's Disease | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Leprosy | Primary Sclerosing Cholangitis | Hyperkeratosis | Lentigo | Bartsocas-Papas Syndrome | Atherosclerosis | Hernia, Inguinal | Metanephric Adenoma | Brooke-Spiegler Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Multiple Hamartoma Syndrome | Adenosine Deaminase Deficiency | Patent Ductus Arteriosus | Sarcoma | Canavan Disease | Clouston Hidrotic Ectodermal Dysplasia | Portal Vein Thrombosis | Osmotic Demyelination Syndrome | Allan-Herndon-Dudley Syndrome | Tuberculous Meningitis | Hyperferritinemia-cataract Syndrome | Keratoacanthoma | Hemorrhagic Disorders | Hepatic 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