Disease

Eclampsia

About the Disease
Eclampsia, also known as eclampsia in puerperium, is related to preeclampsia/eclampsia 1 and severe pre-eclampsia, and has symptoms including seizures An important gene associated with Eclampsia is STOX1 (Storkhead Box 1), and among its related pathways/superpathways are VEGFR1 specific signals and S1P3 pathway. The drugs Azithromycin and Rocuronium have been mentioned in the context of this disorder. Affiliated tissues include kidney, placenta and endothelial, and related phenotypes are homeostasis/metabolism and growth/size/body region

Common Targets
IL12B | IL1RN | LTA | HLA-G | IL1A | OSM | FST | MPO

疾病靶点研报
Eclampsia

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

Other Diseases

Congenital Ichthyosiform Erythroderma | C3 Glomerulonephritis | Polyomavirus Nephropathy | Nance-Horan Syndrome | Patent Foramen Ovale | Arthropathy | Nutrition Disorders | Pseudohypoparathyroidism Type 2 | Noonan Syndrome-like Disorder With Loose Anagen Hair | Diabetes Insipidus | Costello Syndrome | Intracranial Hypertension | Pure Autonomic Failure | Muscle Wasting | Intracerebral Hemorrhage | Fetal And Neonatal Alloimmune Thrombocytopenia | Porphyria Cutanea Tarda | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hepatic Steatosis | Citrullinemia | Borderline Personality Disorder | Obesity | Spinal Muscular Atrophy Type 2 | Vascular Cognitive Impairment | Blepharophimosis Syndrome | Arts Syndrome | Pheochromocytoma | Exocrine Pancreatic Insufficiency | Hypermethioninemia | Persistent Truncus Arteriosus | Depression | Esophagitis | Lymphoma, B-cell | Hyperprolactinemia | Anovulation | Charcot-Marie-Tooth Disease, Type 2 | Pyruvate Carboxylase Deficiency Disease | Vertigo | Fundus Albipunctatus | Pneumoconiosis | McKusick Type Metaphyseal Chondrodysplasia | Pseudohypoparathyroidism Type 1C | Lymphoma Lymphoblastic | Pseudoachondroplasia | Cardiac Sarcoidosis | Neuronal Ceroid Lipofuscinosis | Primary Biliary Cholangitis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Antisynthetase Syndrome | HELLP Syndrome | Kallmann Syndrome | Spinocerebellar Ataxia Type 2 | Insulin Resistance | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Asphyxia Neonatorum | PASLI Disease | Papillon-Lefevre Syndrome | Retinitis | Biotinidase Deficiency | Acute Motor Axonal Neuropathy | Riboflavin Transporter Deficiency Neuronopathy | Glucagonoma | Peeling Skin Syndrome Type B | Myasthenia Gravis | Dystonia | Fibrosis | Persistent Fetal Circulation | Rett Syndrome | Thrombotic Microangiopathy | Hereditary Multiple Exostoses | Impetigo | Restless Legs Syndrome | Viral Meningitis | Gardner Syndrome | Benign Hereditary Chorea | Amelogenesis Imperfecta | Epilepsy Of Infancy With Migrating Focal Seizures | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Aromatic L-amino Acid Decarboxylase Deficiency | Sclerosteosis 2 | Hereditary Hemorrhagic Telangiectasia Type 2 | Anxiety Disorders | Androgenic Alopecia | Craniofacial Dysostosis | Photosensitivity | Multiple Sclerosis, Relapsing-remitting | Silicosis | Hereditary Neuropathy With Liability To Pressure Palsies | Hairy Cell Leukemia | Lipid Metabolism Disorders | Behavioral Variant Of Frontotemporal Dementia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Keratosis | Pure Red Cell Aplasia | Carcinoma, Squamous Cell | Agnathia-Otocephaly Complex | Hemolytic Anemia | Gastritis | Kleine-Levin Syndrome | VACTERL Association | Tenosynovial Giant Cell Tumor | Diabetic Macular Edema | Early Infantile Epileptic Encephalopathy 13 | Vitelliform Macular Dystrophy | Myosin Storage Myopathy | Malignant Peripheral Nerve Sheath Tumor | 3C Syndrome | Pontocerebellar Hypoplasia Type 2 | Multiple System Atrophy | Spinocerebellar Ataxia Type 8 | Senior-Loken Syndrome | Uremia | Erythema Nodosum | Vitiligo | Coronary Artery Disease | Plasma Cell Dyscrasia | Incontinentia Pigmenti | T-cell Chronic Lymphocytic Leukemia | Melnick-Needles Syndrome | Hypertension, Essential | Cirrhosis | Lattice Corneal Dystrophy | Creatine Deficiency Syndrome | Polyneuropathy | Tyrosine Hydroxylase Deficiency | Cri-du-chat Syndrome | Lymphopenia | Phenylketonuria | DRESS Syndrome | Glaucoma | Rash | Glaucomatocyclitic Crisis | Waardenburg Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Lymphomatoid Granulomatosis | Personality Disorders | Trismus-pseudocamptodactyly Syndrome | Ischemia | Autism | Takotsubo Cardiomyopathy | GNE Myopathy | Multiple Hamartoma Syndrome | Charcot-Marie-Tooth Disease Type 2D | Diabetes Mellitus, Transient Neonatal | Congenital Primary Aphakia | Nestor-Guillermo Progeria Syndrome | Larsen Syndrome | X-linked Sideroblastic Anemia | Congenital Adrenal Hyperplasia | Colitis | Anthrax | Lipodystrophy | Low Tension Glaucoma | Carcinoid Syndrome | Hypoglycemia | Osteitis | Bone Giant Cell Tumor | Schizoaffective Disorder | LRBA Deficiency | Primary Sclerosing Cholangitis | FG Syndrome | Renal Tubular Dysgenesis | Hepatitis | Nephronophthisis | Familial Hypobetalipoproteinemia | Neurofibromatosis-Noonan Syndrome | Reye Syndrome | Pterygium | Brachydactyly | Keloid | Astrocytoma | Relapsing Polychondritis | Snyder-Robinson Syndrome | Sporadic Inclusion Body Myositis | Sclerosing Cholangitis | Multisystemic Smooth Muscle Dysfunction Syndrome | Chronic Granulomatous Disease | Swine Influenza | Emery-Dreifuss Muscular Dystrophy | Hartnup Disease | Osmotic Demyelination Syndrome | Glioblastoma Multiforme | Macular Degeneration | Situs Inversus | Pyruvate Dehydrogenase Deficiency | Facioscapulohumeral Muscular Dystrophy Type 1 | Leber Hereditary Optic Neuropathy | Colitis, Lymphocytic | Usher Syndrome Type III | Pseudohermaphroditism | Neutrophilia | Corneal Dystrophy And Perceptive Deafness | Fragile X Syndrome | Eccrine Porocarcinoma | Nevus | Asthma, Exercise-induced | Keratocystic Odontogenic Tumor | Pneumonia, Mycoplasma | Conjunctivitis | Nicotine Addiction | Esophageal Motility Disorders | Spinocerebellar Ataxia Type 6 | Spasticity | Neuromuscular Disorders | Early Infantile Epileptic Encephalopathy 1 | Chromosome 5q Deletion Syndrome | Hereditary Mixed Polyposis Syndrome | Thrombocythemia, Essential | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Myotonic Disorders | IgA Nephropathy | Rheumatoid Arthritis | Congenital Dyserythropoietic Anemia Type 1 | Gastroenteritis, Eosinophilic | Fibronectin Glomerulopathy | Azoospermia | Extramammary Paget's Disease | CDKL5 Deficiency Disorder | Diabetes Type 1 | Schizencephaly | Waardenburg Syndrome Type 2 | Wiskott-Aldrich Syndrome | Stickler Syndrome | Spondylo-ocular Syndrome | Mevalonate Kinase Deficiency | Metanephric Adenoma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Sensorineural Hearing Loss | Krabbe Disease | Hepatic Adenomatosis | Nephrosclerosis | Protein C Deficiency | Brachial Plexus Neuropathy | Kawasaki Disease | Basan Syndrome | Oculocutaneous Albinism | Bethlem Myopathy | Congenital Generalized Lipodystrophy | Rhabdomyosarcoma | Sjogren Syndrome | Cervical Dystonia | Schnyder Crystalline Corneal Dystrophy | Tinea Versicolor | Meningitis | Calcium Pyrophosphate Deposition Disease | Wiedemann-Steiner Syndrome | Primary Torsion Dystonia | Anorectal Fistula | Schwannomatosis | Hypohidrotic Ectodermal Dysplasia | Jawad Syndrome | Gastroschisis | Juvenile Myelomonocytic Leukemia | Epidermolytic Palmoplantar Keratoderma | Encephalitis, Tick-borne | Acromicric Dysplasia | Netherton Syndrome | Micro Syndrome | Palmoplantar Keratoderma | Cocaine-Related Disorders | Fetal Akinesia Deformation Sequence | Erythropoietic Protoporphyria | Cerebral Cavernous Malformations | Autosomal Recessive Bestrophinopathy | Lateral Meningocele Syndrome | Waldenstrom Macroglobulinemia | Tylosis With Esophageal Cancer | Renal Dysplasia | Amyotrophic Lateral Sclerosis, Juvenile | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Hemorrhagic Disorders | 3-methylglutaconic Aciduria Type IV | Epidermolysis Bullosa | Hermansky-Pudlak Syndrome | Hypertension, Pulmonary | Hepatitis B, Chronic | Cancer, Bladder | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Albinism | Hepatitis, Autoimmune | Epithelial-myoepithelial Carcinoma | Carney-Stratakis Syndrome | Infantile Nephropathic Cystinosis | Salla Disease | Congenital Hereditary Endothelial Dystrophy Type II | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Otosclerosis | Anorectal Malformations | Axenfeld-Rieger Syndrome | Carbohydrate Metabolism Disorders | Ovarian Sex Cord-stromal Tumor | Sarcoidosis, Pulmonary | Pleomorphic Xanthoastrocytoma | Myelitis | Follicular Dendritic Cell Sarcoma | Double Outlet Right Ventricle | Acute Leukemia | Atherosclerosis | Spinocerebellar Ataxia Type 42 | Carpal Tunnel Syndrome | Craniofrontonasal Syndrome | Progressive External Ophthalmoplegia | Ichthyosis | Thymoma, Malignant | Iron Overload | Spina Bifida | Blepharo-cheilo-odontic Syndrome | Muscular Dystrophy | Osteopetrosis | Mitochondrial DNA Depletion Syndrome | Saethre-Chotzen Syndrome | Jalili Syndrome | Smith-Lemli-Opitz Syndrome | Genitopatellar Syndrome | Hypertelorism | Cartilage Disorders | Arthritis, Reactive | Juvenile Xanthogranuloma | Focal Facial Dermal Dysplasia | Vitreoretinopathy, Proliferative | Hypoalbuminemia | Angioedema, Hereditary | Carcinoma In Situ | Neurogenic Bladder | Hemangioblastoma | Retinopathy, Diabetic | DiGeorge Syndrome | Bacterial Meningitis | Cardiomyopathy, Restrictive | Congenital Torticollis | Antenatal Bartter Syndrome Type 1 | X-linked Creatine Transporter Deficiency | Focal Segmental Glomerulosclerosis | Hydrocephalus | Charcot-Marie-Tooth Disease Axonal Type 2N | Inflammatory Bowel Disease | Polycythemia Vera | Cellulitis | Microphthalmia, Syndromic 7 | Systemic Mastocytosis | Adrenoleukodystrophy, X-linked | Tibial Muscular Dystrophy | Hamartoma | Progressive Familial Intrahepatic Cholestasis | Lennox-Gastaut Syndrome | Discoid Lupus Erythematosus | Keratitis-ichthyosis-deafness Syndrome | Dermatofibrosarcoma | Galactosialidosis | Renal-hepatic-pancreatic Dysplasia | IgA Deficiency | Glycogen Storage Disease Type 1a | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Gyrate Atrophy Of The Choroid And Retina | Angina Pectoris | Congenital Stromal Corneal Dystrophy | Hypogonadism | Hepatoblastoma | Restrictive Dermopathy | Lupus Erythematosus | Rhizomelic Chondrodysplasia Punctata | Spermatocele | Barakat Syndrome | Pyoderma Gangrenosum | Periventricular Leukomalacia | Obsessive-compulsive Disorder | Diabetes | Herpes Simplex Dermatitis | Urethritis | Congenital Afibrinogenemia | Fuchs Heterochromic Iridocyclitis | Huntington's Disease-like 2 | Autosomal Recessive Spastic Paraplegia Type 75 | Birt-Hogg-Dube Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Atelosteogenesis Type 1 | Hypotonia-cystinuria Syndrome | Hemophilia | Reticular Dysgenesis | Crisponi Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Blomstrand Osteochondrodysplasia | Hypertensive Nephropathy | Alcoholism | Fowler's Syndrome | GATA2 Deficiency | Nager Acrofacial Dysostosis | Primary Hyperoxaluria Type 1 | Oligoastrocytoma | Retinitis Pigmentosa 3 | Cannabis Abuse | Pulmonary Vein Stenosis | Hepatorenal Syndrome | Duchenne Muscular Dystrophy | Congenital Myasthenic Syndrome | Klinefelter Syndrome | Odonto-onycho-dermal Dysplasia | Thrombosis | Sleep Apnea, Obstructive | Large Granular Lymphocytic Leukemia