Reflex Epilepsy

About the Disease
Reflex Epilepsy, also known as epilepsy, reflex, is related to photosensitive epilepsy and episodic kinesigenic dyskinesia 1. An important gene associated with Reflex Epilepsy is SCNM1 (Sodium Channel Modifier 1), and among its related pathways/superpathways are Transmission across Chemical Synapses and Neuroscience. The drugs Valproic acid and Anticonvulsants have been mentioned in the context of this disorder. Affiliated tissues include temporal lobe, cortex and brain, and related phenotypes are nervous system and normal

Common Targets
SCN8A

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

Other Diseases

Sporadic Hemiplegic Migraine | Hypothyroidism | Carotid Artery Disease | Osteogenesis Imperfecta Type III | HANAC Syndrome | Connective Tissue Disorders | Danon Disease | Low Tension Glaucoma | Cancer, Colon | Hyperinsulinemic Hypoglycemia | Neuroendocrine Cancer | Erdheim-Chester Disease | Chondrodysplasia Punctata 2, X-linked Dominant | Epilepsy, Generalized | Mucolipidosis | Gitelman Syndrome | IgA Deficiency | Mitochondrial DNA Depletion Syndrome 13 | Urea Cycle Disorder | Idiopathic Multicentric Castleman Disease | Hypercholesterolemia, Familial | Oligodendroglioma | Neonatal Progeroid Syndrome | Ileitis | Borderline Personality Disorder | Acromesomelic Dysplasia | Myasthenia Gravis | Feingold Syndrome | Malaria, Cerebral | Pneumococcal Meningitis | Skin Fragility-woolly Hair Syndrome | Odonto-onycho-dermal Dysplasia | Epithelial-myoepithelial Carcinoma | Rothmund-Thomson Syndrome | Early Infantile Epileptic Encephalopathy 1 | Chronic Myelomonocytic Leukemia | Chloridorrhea, Congenital | Acrocallosal Syndrome | Hypertelorism | Focal Dermal Hypoplasia | Kallmann Syndrome | Schizophrenia, Paranoid | Waardenburg Syndrome | Glioblastoma Multiforme | Persistent Fetal Circulation | Amyotrophic Lateral Sclerosis | Ichthyosis, X-linked | Congenital Stationary Night Blindness | Isovaleric Acidemia | Leishmaniasis, Cutaneous | Colon Adenoma | Autism Spectrum Disorders | Myotonia | Frontometaphyseal Dysplasia | Keratoacanthoma | Multiple Sclerosis, Secondary Progressive | Multicentric Carpotarsal Osteolysis Syndrome | Orthostatic Intolerance | Lymphomatoid Granulomatosis | Sulfite Oxidase Deficiency | Pneumonia, Viral | Cryoglobulinemia | Uterine Leiomyoma | Pycnodysostosis | Rhabdomyosarcoma, Embryonal | Vertigo | Glomerulonephritis, Membranoproliferative | Charcot-Marie-Tooth Disease Type 2D | Pulmonary Vein Stenosis | Chronic Granulomatous Disease | Cancer, Skin | Keratosis, Actinic | Congenital Myopathy | Familial Digital Arthropathy-brachydactyly | Creutzfeldt-Jakob Disease | Retinal Telangiectasia | Carcinoma, Small Cell | Hypercalciuria | Preaxial Polydactyly | Episodic Ataxia Type 2 | Immunoproliferative Disorders | Thrombophlebitis | Still Disease | Tonsillitis | Actinomycetoma | Paraganglioma | Pendred Syndrome | Zygomycosis | Peutz-Jeghers Syndrome | Monilethrix | Hereditary Hemorrhagic Telangiectasia | Hernia, Inguinal | Bone Marrow Necrosis | Polycystic Kidney, Autosomal Recessive | Mohr-Tranebjaerg Syndrome | Hyperekplexia | Creatine Deficiency Syndrome | Tenosynovial Giant Cell Tumor | Charcot-Marie-Tooth Disease Type 4E | Gilbert Syndrome | Rhabdomyosarcoma, Alveolar | Lymphoma, Primary Cutaneous Anaplastic Large Cell | MIRAGE Syndrome | Polymyalgia Rheumatica | Blue Rubber Bleb Nevus Syndrome | Periventricular Nodular Heterotopia | Postpoliomyelitis Syndrome | Atopic Dermatitis | Basal Ganglia Disease | Erythema Multiforme | Gastroenteritis, Eosinophilic | Extramammary Paget's Disease | Carcinoma, Merkel Cell | Osteogenesis Imperfecta | Double Outlet Right Ventricle | Autosomal Recessive Spastic Paraplegia Type 54 | Silver-Russell Syndrome | Sponastrime Dysplasia | Spinocerebellar Ataxia Type 31 | Botulism | Norrie Disease | Evans Syndrome | Obesity, Morbid | Benign Recurrent Intrahepatic Cholestasis 1 | Corneal Dystrophies, Hereditary | Harlequin Ichthyosis | Smoldering Myeloma | Larsen Syndrome | Bethlem Myopathy | Perivascular Epithelioid Cell Tumor | Arthritis, Gouty | Onchocerciasis | Hyperinsulinemia | Pemphigus Foliaceus | Hemimegalencephaly | Presbyopia | X-linked Creatine Transporter Deficiency | Smith-Lemli-Opitz Syndrome | Mixed Connective Tissue Disease | MELAS Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Hypotension, Orthostatic | Megaloblastic Anemia | Spinocerebellar Ataxia Type 20 | Pierson Syndrome | Cenani-Lenz Syndactyly Syndrome | Glycogen Storage Disease Type 6 | Glycogen Storage Disease Type 9 | Thyroiditis | Cataplexy | Distal Myopathy | Succinic Semialdehyde Dehydrogenase Deficiency | Pemphigus Vulgaris | Adrenomyeloneuropathy | Steel Syndrome | Cardiac Arrest | Hartsfield Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Corneal Neovascularization | Dentinogenesis Imperfecta | Fibronectin Glomerulopathy | Trigonocephaly | Cardiofaciocutaneous Syndrome | Antithrombin III Deficiency | Eosinophilic Asthma | Maple Syrup Urine Disease | Amish Infantile Epilepsy Syndrome | Kabuki Syndrome 2 | Endometrial Hyperplasia | Hypogonadism | Conduct Disorder | Hepatoblastoma | ICF Syndrome | Mesothelioma, Malignant | Arrhythmogenic Right Ventricular Cardiomyopathy | Wilson's Disease | Loeys-Dietz Syndrome | Dystonia Musculorum Deformans | Epidermolysis Bullosa Simplex, Dowling-Meara Type | L-2-Hydroxyglutaric Aciduria | Meningioma | Aicardi-Goutieres Syndrome | Congenital Diaphragmatic Hernia | Wolfram Syndrome 2 | Pulmonary Sclerosing Hemangioma | Insulinoma | Bietti Crystalline Dystrophy | Vascular Calcification | Malignant Fibrous Histiocytoma | Common Cold | Axenfeld-Rieger Syndrome | Spinal And Bulbar Muscular Atrophy | Hemosiderosis | Early Infantile Epileptic Encephalopathy 4 | Arthritis | Takotsubo Cardiomyopathy | Hepatopulmonary Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Spinocerebellar Ataxia Type 21 | Giant Cell Glioblastoma | Behcet's Disease | Spinocerebellar Ataxia Type 3 | Agammaglobulinemia | Raine Syndrome | Megalencephaly | Congenital Hereditary Endothelial Dystrophy Type II | Familial Advanced Sleep Phase Syndrome | Learning Disability | Glucagonoma | Tendinopathy | Spinocerebellar Ataxia Type 5 | Granular Corneal Dystrophy | Dermatofibrosarcoma | Kaposi Sarcoma | Paternal Uniparental Disomy Of Chromosome 14 | Opisthorchiasis | Angiodysplasia | Chiari Malformation Type I | Angelman Syndrome | Transient Bullous Dermolysis Of The Newborn | Cockayne Syndrome | Diabetes Type 2 | Mucolipidosis Type II | Myeloid Leukemia | Heroin Dependence | Chudley-McCullough Syndrome | Cerebrotendinous Xanthomatosis | Charcot-Marie-Tooth Disease Type 3 | Ganglioglioma | TARP Syndrome | Blepharitis | Cryptococcal Meningitis | Keratosis | Duane Retraction Syndrome | Muscular Dystrophy | Guanidinoacetate Methyltransferase Deficiency | Renpenning Syndrome | Neurocutaneous Melanocytosis | Sjogren Syndrome | Neovascular Glaucoma | Granuloma Annulare | POEMS Syndrome | Bardet-Biedl Syndrome | DEND Syndrome | Trichotillomania | Priapism | Myosin Storage Myopathy | Phenylketonuria II | Cocaine-Related Disorders | Congenital Generalized Lipodystrophy | Pathological Gambling | Crimean-Congo Hemorrhagic Fever | Hyperferritinemia-cataract Syndrome | Hereditary Multiple Exostoses | Autosomal Recessive Congenital Ichthyosis | Varices | Arteriosclerosis | Headache | DOCK8 Immunodeficiency Syndrome | Gray Platelet Syndrome | Osteoporosis-pseudoglioma Syndrome | Neuropathy | Lentigo | T-cell Leukemia | Antley-Bixler Syndrome | Hemophagocytic Lymphohistiocytosis | Multiple Sclerosis, Chronic Progressive | Fontaine Progeroid Syndrome | Hemochromatosis | Oguchi Disease-2 | Eiken Syndrome | Lysosomal Acid Lipase Deficiency | Pemphigus | Glioma | Pregnancy, Ectopic | Hyperparathyroidism | Facioscapulohumeral Muscular Dystrophy Type 1 | Hereditary Folate Malabsorption | Myopathy | Tyrosinemia | Choriocarcinoma | Galactosemia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Lennox-Gastaut Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Viral Meningitis | Bladder Exstrophy | Bipolar Disorder | Porphyria Cutanea Tarda | Low Phospholipid Associated Cholelithiasis | Autonomic Neuropathy | Alazami Syndrome | LMNA-related Congenital Muscular Dystrophy | Optic Neuropathy | Primary Erythromelalgia | Hypertension, Essential | Endometriosis | Lymphangioleiomyomatosis | Acute Lung Injury | Glycogen Storage Disease | Myocarditis | Shock, Cardiogenic | Sleep Disorder | Homocystinuria | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Sialoadenitis | Anthrax | Porphyria | Peeling Skin Syndrome Type B | Paraplegia | Central Core Disease | Alpha-thalassemia Myelodysplasia Syndrome | Carney Triad | Diabetes Mellitus, Transient Neonatal | Esophageal Carcinoma | Parkinson's Disease | Optic Nerve Diseases | Osteogenesis Imperfecta Type VI | Pulmonary Tuberculosis | Glycogen Storage Disease Type 1b | Hemangioendothelioma | Pyloric Stenosis, Infantile Hypertrophic | Hemochromatosis Type 1 | McCune-Albright Syndrome | Joubert Syndrome 2 | Hepatitis D | Colitis, Collagenous | Exocrine Pancreatic Insufficiency | Neurodevelopmental Disorders | Meckel-Gruber Syndrome | Tendinitis | Primary Biliary Cholangitis | McKusick Type Metaphyseal Chondrodysplasia | Osteonecrosis Of The Jaw | Sick Sinus Syndrome 1 | Charcot-Marie-Tooth Disease, Type 2A | Pituitary Disorders | Sarcoma | Nemaline Myopathy | Autonomic Nervous System Disorders | Kohlschutter-Tonz Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Schnitzler Syndrome | Tyrosine Hydroxylase Deficiency | Mitochondrial DNA Depletion Syndrome | Hypertension, Renal | Hypertension, Renovascular | Fragile X Syndrome | Schamberg Disease | Acrodermatitis Enteropathica | Cavitary Optic Disc Anomalies | Iron Metabolism Disorders | Apert Syndrome | Lichen Sclerosus | Retinal Diseases | Inflammatory Myopathy | Mosaic Variegated Aneuploidy Syndrome 2 | Cardiomyopathy, Hypertrophic | Dominant Optic Atrophy | Coffin-Siris Syndrome | Inflammatory Joint Disease | Amelanotic Melanoma | Spinal Muscular Atrophy Type 2 | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Intermittent Claudication | Usher Syndrome Type IIC | Congenital Nystagmus | Mumps | Yellow Fever | Acromicric Dysplasia | Measles | Albinism | Cancer, Breast | Diabetic Nephropathy | Atelosteogenesis Type 1 | Hepatitis C, Chronic | Schizophrenia | Temtamy Preaxial Brachydactyly Syndrome | Adenoma, Villous | Waardenburg Syndrome Type 4 | Japanese Encephalitis | Progressive Familial Intrahepatic Cholestasis Type 2 | Stevens-Johnson Syndrome | Autosomal Recessive Bestrophinopathy | Intracranial Hypertension | Proximal Symphalangism | Greenberg Dysplasia | SAPHO Syndrome | Tyrosinemia Type 2 | Leukoplakia, Oral | Primary Hyperoxaluria | Wolman Disease | Pericarditis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Beta-Propeller Protein-associated Neurodegeneration | Brachial Plexus Neuropathy | Hyperuricemic Nephropathy, Familial Juvenile | Brenner Tumor | Polymyositis | Hereditary Inclusion Body Myopathy