Disease

Toxoplasmosis

About the Disease
Toxoplasmosis, also known as multisystemic disseminated toxoplasmosis, is related to congenital toxoplasmosis and meningoencephalitis, and has symptoms including fever and pruritus. An important gene associated with Toxoplasmosis is CD40LG (CD40 Ligand), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Valproic acid and Sulfadiazine have been mentioned in the context of this disorder. Affiliated tissues include brain, eye and bone marrow, and related phenotypes are Synthetic lethal with MLN4924 (a NAE inhibitor) and Synthetic lethal with MLN4924 (a NAE inhibitor)

Common Targets
NADPH Oxidase (nonspecified subtype) | HLA-C | IL10 | ADK | G7124 | IL1B | G6774 | ADP-Ribosyl Cyclase/cyclic ADP-Ribose Hydrolase (ADPRC) (nonspecified subtype) | TYR | NOD2 | HLA-B | G7099 | Chaperone (nonspecified subtype) | Histone acetyltransferase (HAT) (nonspecified subtype) | CD38 | PRKD3 | IL1A | NOX3 | TLR9 | NADPH Oxidase Complex | P2RX7 | IFNG | MICA | DHFR

疾病靶点研报
Toxoplasmosis

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

Other Diseases

Carbonic Anhydrase VA Deficiency | Epiphyseal Chondrodysplasia, Miura Type | Conn Syndrome | Mucolipidosis Type III | Non-proliferative Diabetic Retinopathy | Scoliosis | Chromosome 9q34.3 Deletion Syndrome | Spinocerebellar Ataxia Type 27 | Gliosarcoma | Asthma, Exercise-induced | Leber Congenital Amaurosis | Glycogen Storage Disease Type 1 | Arthrogryposis | Niemann-Pick Disease, Type C | Diabetic Nephropathy | Oral Lichen Planus | Pupil Disorders | Robinow Syndrome | Pituitary Dwarfism | Chediak-Higashi Syndrome | Lesch-Nyhan Syndrome | Mountain Sickness | Central Retinal Artery Occlusion | Pericarditis | Apraxia | Azoospermia | Sweet Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Ehlers-Danlos Syndrome | Onchocerciasis | Glomerulonephritis | Mitochondrial Disease | Toxic Epidermal Necrolysis | Graft-versus-host Disease | Cholangitis | Familial Male-limited Precocious Puberty | Intestinal Pseudo-obstruction | Corticobasal Syndrome | Schuurs-Hoeijmakers Syndrome | Obesity | 3C Syndrome | Phenylketonuria | Aicardi-Goutieres Syndrome | Hemosiderosis | Familial Partial Lipodystrophy | Premenstrual Syndrome | Connective Tissue Disorders | Hemochromatosis | Cholesteryl Ester Storage Disease | Angiosarcoma | Nephrocalcinosis | Multiple Myeloma | Periventricular Nodular Heterotopia | Leukoplakia, Oral | Adenosine Deaminase Deficiency | Absence Epilepsy | Oculocutaneous Albinism Type 2 | Multisystemic Smooth Muscle Dysfunction Syndrome | Bardet-Biedl Syndrome | Rosacea | Congenital Mirror Movements | Scapuloperoneal Spinal Muscular Atrophy | Blepharophimosis Syndrome | Coma | Parapsoriasis | Cerebellar Ataxia, Cayman Type | Alopecia Totalis | N-acetylglutamate Synthase Deficiency | Sickle Cell Disease | Diabetes | Endometriosis | Keratocystic Odontogenic Tumor | Lipid Storage Myopathy | Imerslund-Grasbeck Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Cutaneous Angiosarcoma | Traboulsi Syndrome | Postaxial Polydactyly | Hereditary Hemorrhagic Telangiectasia | Addison Disease | Melanoma, Malignant | Hemolytic Uremic Syndrome, Atypical | Carcinoma, Squamous Cell | Oculocutaneous Albinism | Prolymphocytic Leukemia | Epidermolysis Bullosa Simplex, Generalized | X-linked Myotubular Myopathy | Dentinogenesis Imperfecta | Auriculocondylar Syndrome | Norrie Disease | Generalized Epilepsy And Paroxysmal Dyskinesia | Glioma | Hypospadias | Bursitis | Bernard-Soulier Syndrome | Kohlschutter-Tonz Syndrome | Polymyositis | Lymphoproliferative Disorders | Hypodontia | Tyrosinemia | Delayed Sleep Phase Syndrome | Joubert Syndrome 2 | Mycosis Fungoides | Prostatitis | Bietti Crystalline Dystrophy | Epidermolysis Bullosa Dystrophica | Spondylometaphyseal Dysplasia | Retinitis Pigmentosa | Thrombophilia | Chitayat Syndrome | Optic Nerve Diseases | Spinocerebellar Ataxia Type 16 | Myofibrillar Myopathy | Pontocerebellar Hypoplasia Type 7 | Encephalopathy, Hepatic | Anti-NMDA Receptor Encephalitis | Thalassemia | Posterior Polar Cataract | Measles | Congenital Bilateral Absence Of Vas Deferens | Lyme Disease | Renpenning Syndrome | Maternally Inherited Diabetes And Deafness | Arts Syndrome | Porphyria, Variegate | Mesothelioma, Malignant | Non-Hodgkin Lymphoma | Genee-Wiedemann Syndrome | Congenital Hypofibrinogenemia | Pneumococcal Meningitis | Rubeosis Iridis | Hypothyroidism | Meningococcal Infections | Cancer, Kidney | Marinesco-Sjogren Syndrome | Trichothiodystrophy | Craniosynostosis | Pulmonary Alveolar Proteinosis | Spinocerebellar Ataxia Type 28 | Neurofibromatosis Type 2 | Myasthenia | Osteoporosis | Tendinopathy | Atelosteogenesis Type 2 | Jalili Syndrome | Centronuclear Myopathy | Lafora Disease | Inborn Errors Of Metabolism | Thyrotoxic Periodic Paralysis | Cantu Syndrome | Pyruvate Decarboxylase Deficiency | Superficial Spreading Melanoma | Diverticulitis | Anovulation | Primary Lateral Sclerosis | Alzheimer Disease, Late Onset | Diabetic Macular Edema | Coffin-Siris Syndrome | Esophageal Carcinoma | Crigler-Najjar Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Pilomatrix Carcinoma | Constipation | HANAC Syndrome | Synpolydactyly | Bartter Syndrome | Fibrodysplasia Ossificans Progressiva | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Spastic Paraplegia Type 7 | Malignant Fibrous Histiocytoma | Campomelic Dysplasia | Rhabdomyosarcoma, Alveolar | Glutaric Aciduria Type 3 | Blepharitis | Phosphoglycerate Dehydrogenase Deficiency | Beare-Stevenson Syndrome | Metachromatic Leukodystrophy | Abetalipoproteinemia | Unverricht-Lundborg Syndrome | Osteomyelitis | Orthostatic Intolerance | Acute Chest Syndrome | Granular Corneal Dystrophy | Pleural Tuberculosis | Nicotine Addiction | Huntington's Disease | Intracerebral Hemorrhage | Chronic Kidney Disease | Familial Mediterranean Fever | Rhabdoid Tumor | Juvenile Myelomonocytic Leukemia | Lymphoma, AIDS-related | Pregnancy, Ectopic | Batten Disease | Hereditary Spastic Paraplegia | Spinal Muscular Atrophy Type 3 | Goiter | Macrophage Activation Syndrome | Cannabis Abuse | Leber Hereditary Optic Neuropathy | Hypertension, Portal | Gaucher Disease | Chloridorrhea, Congenital | Myofibromatosis | Hypertension, Pulmonary | Angiosarcoma Of The Breast | Blepharospasm | Hepatorenal Syndrome | Encephalitis, Tick-borne | Guttate Psoriasis | Ameloblastic Carcinoma | Prolactinoma | X-linked Charcot-Marie-Tooth Disease | Chondrodysplasia Punctata 2, X-linked Dominant | Orotic Aciduria | Early Infantile Epileptic Encephalopathy 13 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Neurofibromatosis Type 1 | Mabry Syndrome | Xeroderma Pigmentosum Variant Type | Adrenal Insufficiency | Hydrolethalus Syndrome | Arthritis, Psoriatic | Birt-Hogg-Dube Syndrome | Cone Dystrophy | Pseudoachondroplasia | Pachyonychia Congenita | Diabetes Type 2 | Ocular Hypertension | Chorea-acanthocytosis | Swine Influenza | Crouzon Syndrome With Acanthosis Nigricans | Chondrodysplasia Punctata 1, X-linked Recessive | Situs Inversus | Prurigo Nodularis | Pseudoexfoliation Syndrome | Melanoma | Currarino Syndrome | Plasma Cell Leukemia | Glucagonoma | Danon Disease | Kallmann Syndrome | Ulcerative Colitis | Nasodigitoacoustic Syndrome | Hidradenitis Suppurativa | Acrodermatitis | Fuchs Heterochromic Iridocyclitis | Hepatitis, Alcoholic | Nephrotic Syndrome Type 1 | Meningococcal Meningitis | Peeling Skin Syndrome Type B | Diabetes Insipidus | DNA Ligase IV Deficiency | Glaucoma | Spinocerebellar Ataxia Type 8 | Spinocerebellar Ataxia Type 13 | Hypertension, Renal | Congenital Hereditary Endothelial Dystrophy Type II | Kabuki Syndrome | Tumoral Calcinosis | Vascular Cognitive Impairment | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Adenoid Cystic Carcinoma | Farber Disease | Aphasia | Hypertension | Takenouchi-Kosaki Syndrome | Recurrent Respiratory Papillomatosis | Hyperuricemia | GATA2 Deficiency | Adenomyosis | C3 Glomerulopathy | Saul-Wilson Syndrome | Hypogammaglobulinemia | Dyslipidemia | Glycogen Storage Disease Type 0 | Scleritis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Malaria | Pain | Long QT Syndrome Type 3 | Parkinsonism | Meniere's Disease | Isobutyryl-CoA Dehydrogenase Deficiency | Holt-Oram Syndrome | Metatropic Dysplasia | IMAGe Syndrome | Cyst | Congenital Myasthenic Syndrome | Thrombocytopenia | Rotor Syndrome | Multiple Hamartoma Syndrome | Cholestasis, Intrahepatic | Corneal Neovascularization | Arteriosclerosis | Primary Torsion Dystonia | Sensory Neuropathy | Disseminated Superficial Actinic Porokeratosis | Alpers Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Carbohydrate Metabolism Disorders | Borjeson-Forssman-Lehmann Syndrome | Gingivitis | Coronary Heart Disease | Congenital Nystagmus | Hyperthermia, Malignant | Dysthymia | Long QT Syndrome Type 1 | Nager Acrofacial Dysostosis | Palmoplantar Keratoderma | Endophthalmitis | Glaucoma, Congenital | Camurati-Engelmann Disease | Priapism | Diabetic Neuropathy | Asplenia | Thromboembolism | Infantile Refsum Disease | Li-Fraumeni Syndrome | Sclerosing Cholangitis | Leukoplakia | Nail-Patella Syndrome | Cystitis, Interstitial | 3-hydroxy-3-methylglutaric Aciduria | Plasma Cell Dyscrasia | Mucolipidosis Type IV | Acute Kidney Injury | Sarcoma, Alveolar Soft Part | Fontaine Progeroid Syndrome | 5-oxoprolinase Deficiency | Anuria | Gout | Blau Syndrome | Leiomyosarcoma | Primary Carnitine Deficiency | Chudley-McCullough Syndrome | Idiopathic Multicentric Castleman Disease | Charcot-Marie-Tooth Disease Type 2D | Acral Lentiginous Melanoma | Amelogenesis Imperfecta | Malignant Peripheral Nerve Sheath Tumor | McCune-Albright Syndrome | Hyperthyroidism | Fanconi Anemia | Renal Dysplasia | Acromicric Dysplasia | Coronary Restenosis | Portal Vein Thrombosis | Corneal Edema | Erythematotelangiectatic Rosacea | Lymphedema | Metabolic Diseases | Growth Hormone Excess | Persistent Fetal Circulation | Sialoadenitis | Adenocarcinoma | Asperger Syndrome | Vitamin D Deficiency | Pseudohypoparathyroidism Type 2 | Familial Digital Arthropathy-brachydactyly | Feingold Syndrome | Mitochondrial Cytopathy | Otitis Media | Chiari Malformation Type I | Benign Familial Neonatal Convulsions | Hemolytic Anemia | Nemaline Myopathy 8 | Obsessive-compulsive Disorder | Dent Disease | Giant Cell Arteritis | Waardenburg Syndrome Type 2E | Hypercalciuria | CEDNIK Syndrome | Optic Neuropathy | Conduct Disorder | Leigh Syndrome | Congenital Stromal Corneal Dystrophy | Hypotrichosis | Tyrosinemia Type 2 | Moyamoya Disease | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Shock, Cardiogenic | Familial Hypertrophic Cardiomyopathy | Hepatitis A | Acrocallosal Syndrome | Cutaneous T-cell Lymphoma | Hemangioendothelioma | Pseudohypoparathyroidism Type 1B | Dyggve-Melchior-Clausen Disease | Craniofacial Dysostosis | Schnitzler Syndrome | Basal Ganglia Cerebrovascular Disease | Avian Influenza | Olmsted Syndrome | Genitopatellar Syndrome | Homocystinuria | Seizures-scoliosis-macrocephaly Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | POEMS Syndrome | Retinitis