Disease

Seizures

About the Disease
Visual Epilepsy, also known as seizures, is related to spinal muscular atrophy with progressive myoclonic epilepsy and photosensitive epilepsy, and has symptoms including seizures An important gene associated with Visual Epilepsy is BDNF-AS (BDNF Antisense RNA). The drugs Ibuprofen and Diclofenac have been mentioned in the context of this disorder. Affiliated tissues include temporal lobe, brain and cortex.

Common Targets
G7099 | LRRK2 | Integrin alpha4beta1 (VLA-4) receptor | CACNA2D1 | OPRM1 | L-type voltage-dependent calcium channel complex | PPARA | MIR134 | SLC19A3 | RNF115 | MGLL | ALDH2 | KCNQ3 | SLC7A11 | PLPBP | TRPM8 | GABRB2 | GABRG2 | PCDH19 | NEDD4L | CNR1 | CPT1A | G7124 | DBH | DYRK1A | CDKN2B-AS1 | PRRT2 | GABA(A) receptor | TRPV1 | TRPV2 | TDP2 | TBC1D24 | Opioid receptor (nonspecified subtype) | TIRAP | SV2C | PPARD | KLHL29 | TSC2 | HNRNPU | Voltage-Gated Sodium Channel Complex | SZT2 | GSK3B | UGT2B7 | QARS1 | Sodium channel (nonspecified subtype) | GABRA1 | FAAH | IL1A | KCNQ1 | SCN1A | L-Type calcium channel (nonspecified subtype) | TLR9 | SNAP25 | ERBB4 | KCNMA1 | METTL23 | TRPA1 | MGMT | ITGB3 | GABRD | RBSN | KCNJ10 | SLC6A3 | ABAT | SLC1A2 | SCN5A | CNNM2 | KCNQ2 | CYP3A4 | GSK3A | KCND2 | Glutamate Receptor Ionotropic AMPA Receptor | SCN2A | SV2A | HRH3

疾病靶点研报
Seizures

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

Other Diseases

Spinocerebellar Ataxia Type 14 | Dementia, Vascular | Arthrogryposis | Apparent Mineralocorticoid Excess Syndrome | Epidermolysis Bullosa Simplex, Localized | Osteochondrosis | Lentigo | Vitreoretinopathy, Proliferative | Specific Granule Deficiency | Micro Syndrome | Colitis, Lymphocytic | Dysmorphophobia | Blepharitis | Craniopharyngioma | Chronic Neutrophilic Leukemia | Osteonecrosis | Cocaine-Related Disorders | Sweet Syndrome | Sertoli Cell-only Syndrome | Myelitis, Transverse | Bloom Syndrome | Inflammatory Joint Disease | Spinal Muscular Atrophy | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Pemphigoid | Acrodermatitis | Usher Syndrome | Carney-Stratakis Syndrome | Hypotension, Orthostatic | Cockayne Syndrome | Stiff-man Syndrome | Mucolipidosis Type II | Progressive Familial Intrahepatic Cholestasis Type 1 | REM Sleep Behavior Disorder | Pouchitis | Hyperostosis | Neuroleptic Malignant Syndrome | Van Der Knaap Disease | Chromosome 5q Deletion Syndrome | Cystinosis | Cardiospondylocarpofacial Syndrome | Fetal Alcohol Syndrome | Prostatitis | Porencephaly | Congenital Heart Block | Dyggve-Melchior-Clausen Disease | Arthritis, Gouty | Epidermal Nevus Syndrome | Anti-NMDA Receptor Encephalitis | Distal Myopathy 2 | Hydrocephalus, Normal Pressure | Spitz Nevus | Joubert Syndrome | Ectrodactyly | Gaucher Disease | Familial Glucocorticoid Deficiency | Coronary Restenosis | Ellis-Van Creveld Syndrome | Hydronephrosis | Cancer, Colon | Charcot-Marie-Tooth Disease Type 4B1 | Farber Disease | Melanoma, Uveal | Rhizomelic Chondrodysplasia Punctata | Gestational Trophoblastic Disease | Swine Influenza | Epidermolysis Bullosa Simplex, Generalized | Methemoglobinemia Type IV | Stroke, Ischemic | Wolfram Syndrome 2 | Megalencephaly | Panic Disorder | Gray Platelet Syndrome | Neurocysticercosis | Amyotrophic Lateral Sclerosis, Juvenile | Lymphoproliferative Disorders | Loeys-Dietz Syndrome | Turner's Syndrome | Hyperthermia, Malignant | Cerebral Cavernous Malformations | Schistosomiasis Mansoni | Neuromyotonia | Hypermethioninemia | Localized Scleroderma | Fabry's Disease | Muckle-Wells Syndrome | Retinopathy, Diabetic | Hypolipoproteinemia | Rheumatoid Arthritis | Cryoglobulinemia | Retinoblastoma | Hepatitis A | Myosin Storage Myopathy | Nicotine Addiction | Osteogenesis Imperfecta Type V | Acute Kidney Injury | Williams Syndrome | Hemorrhoids | Stuve-Wiedemann Syndrome | Peutz-Jeghers Syndrome | Cellulitis | Osteopetrosis | Atopy | Purpura | Cystitis, Interstitial | Neonatal Progeroid Syndrome | Granular Corneal Dystrophy Type 1 | Greig Cephalopolysyndactyly Syndrome | Pancreatitis | Usher Syndrome Type IIC | Keratopathy | Microvillus Inclusion Disease | Choriocarcinoma | Richter's Syndrome | Peyronie's Disease | Apert Syndrome | Presbyopia | Gerstmann-Straussler-Scheinker Syndrome | Anxiety Disorders | Carbonic Anhydrase VA Deficiency | Multicystic Renal Dysplasia | Zellweger Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Ameloblastoma | Esophageal Carcinoma | 3-methylcrotonyl-CoA Carboxylase Deficiency | Cholangitis | Hyperbilirubinemia | Angiosarcoma Of The Breast | Spinocerebellar Ataxia Type 7 | Keratitis-ichthyosis-deafness Syndrome | Leigh Syndrome | Corneal Dystrophy | Corticobasal Syndrome | Parvovirus B19 Infection | CEDNIK Syndrome | Charcot-Marie-Tooth Disease | Brenner Tumor | Dengue Shock Syndrome | Retinopathy Of Prematurity | Oligoastrocytoma | Mitochondrial Cytopathy | Alpha-1 Antitrypsin Deficiency | Fanconi Anemia | Kearns-Sayre Syndrome | Niemann-Pick Disease | Pneumococcal Meningitis | Acral Lentiginous Melanoma | Heimler Syndrome | Lipid Storage Myopathy | Idiopathic Multicentric Castleman Disease | Vascular Cognitive Impairment | Persistent Fetal Circulation | Hepatitis, Autoimmune | Lyme Disease | Pyruvate Decarboxylase Deficiency | Palsy, Cerebral | Sialidosis Type I | Huntington's Disease-like 2 | Spondylocostal Dysostosis | Krabbe Disease | Paraganglioma | Spinocerebellar Ataxia Type 6 | Synovitis | Hypoglycemia | Norrie Disease | Neuroma | Subacute Sclerosing Panencephalitis | Spina Bifida | Autoimmune Polyendocrinopathy Syndrome Type I | X-linked Creatine Transporter Deficiency | Mitochondrial Disease | Insulin Resistance | Pleomorphic Xanthoastrocytoma | Saul-Wilson Syndrome | Sezary Syndrome | Episodic Ataxia Type 1 | Avellino Corneal Dystrophy | Smoldering Myeloma | Esophageal Motility Disorders | Sarcoma, Endometrial Stromal | Cerebellar Ataxia, Cayman Type | Necrobiosis Lipoidica | Corneal Edema | Cerebrotendinous Xanthomatosis | Amenorrhea | Zollinger-Ellison Syndrome | Tumoral Calcinosis | Meckel-Gruber Syndrome | Sarcoma, Ewing | 5-oxoprolinase Deficiency | Spinocerebellar Ataxia | Haim-Munk Syndrome | Spitzoid Melanoma | Fragile X Syndrome | Neuroendocrine Cancer | Keratitis | Basal Ganglia Disease | Parkinsonism | Acromegaly | Micropenis | Polyarteritis Nodosa | Carcinoid Tumor | Camurati-Engelmann Disease | Enterocolitis, Necrotizing | Agnathia-Otocephaly Complex | Thromboembolism | Neural Tube Defect | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Scapuloperoneal Myopathy, X-linked Dominant | Multiple Epiphyseal Dysplasia | Hypermetropia | Impulse Control Disorder | Language Disorders | Retinal Detachment | Branchiootorenal Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Adult Polyglucosan Body Disease | Trichotillomania | Vertigo | Myasthenia Gravis | Burn-McKeown Syndrome | Spinocerebellar Ataxia Type 5 | Epidermolysis Bullosa Dystrophica | Thyroid Dysgenesis | Myositis | Erythropoietic Protoporphyria | Hemoglobinopathies | Paroxysmal Nocturnal Hemoglobinuria | Asthma, Exercise-induced | Blepharoconjunctivitis | Echinococcosis | Behcet's Disease | Antisynthetase Syndrome | Myelofibrosis | Agoraphobia | Demyelinating Diseases | 3-methylglutaconic Aciduria Type IV | Cystinuria | Mucormycosis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Aldosterone Synthase Deficiency | Chronic Granulomatous Disease | Portal Vein Thrombosis | Hyperparathyroidism-jaw Tumor Syndrome | Hidradenitis Suppurativa | WAGR Syndrome | Spinocerebellar Ataxia Type 27 | Mitochondrial Myopathy | Depression | Sjogren Syndrome | Cerebrovascular Disorders | Duchenne Muscular Dystrophy | Focal Dermal Hypoplasia | Diabetes Insipidus, Nephrogenic | Combined Deficiency Of Factor V And Factor VIII | Hyperuricemia | Stroke, Hemorrhagic | Focal Cortical Dysplasia Type 2 | Hidradenitis | Fibrillation, Atrial | Diabetes Type 2 | Glycogen Storage Disease Type 1a | Cluster Headache | Aphasia | Angelman Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Otosclerosis | Prolidase Deficiency | Hyperinsulinism-hyperammonemia Syndrome | Hypoplastic Left Heart Syndrome | Hypercholesterolemia | Alopecia Totalis | Malaria, Cerebral | Congenital Fiber-type Disproportion Myopathy | Adenoma, Villous | Endocarditis | Congenital Muscular Dystrophy | Scapuloperoneal Spinal Muscular Atrophy | Ependymoma | Fetal And Neonatal Alloimmune Thrombocytopenia | Intermittent Explosive Disorder | Apraxia | Sleep Apnea, Obstructive | Congenital Bilateral Absence Of Vas Deferens | Dyskeratosis Congenita | Congenital Adrenal Hyperplasia 1 | Cancer, Bladder | Leri-Weill Dyschondrosteosis | Tyrosinemia Type 1 | Relapsing Polychondritis | Ichthyosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Exocrine Pancreatic Insufficiency | Neurofibromatosis Type 2 | Niemann-Pick Disease, Type B | Osteogenesis Imperfecta Type I | Leprosy | Olmsted Syndrome | Lymphangiomatosis | Pupil Disorders | Roberts Syndrome | Hyperinsulinemic Hypoglycemia | Zimmermann-Laband Syndrome | Esthesioneuroblastoma | Astigmatism | Goiter, Nodular | Malaria | LRBA Deficiency | Hypertension, Portal | Polydactyly | Osteogenesis Imperfecta Type IV | Panuveitis | Retinal Degeneration | Carney Triad | Tonsillitis | Triple A Syndrome | Thrombophilia | Mabry Syndrome | Congenital Hypofibrinogenemia | Muscular Dystrophy | CREST Syndrome | Stromal Corneal Dystrophy | Glycogen Storage Disease Type 0 | Erectile Dysfunction | Aplastic Anemia | Spondylosis | Microcephalic Primordial Dwarfism | Craniosynostosis | Dermatomyositis | Anovulation | Spondylometaphyseal Dysplasia | Unverricht-Lundborg Syndrome | Otitis Media | Poirier-Bienvenu Neurodevelopmental Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Influenza | Spinocerebellar Ataxia Type 20 | Hypophosphatasia | Hepatic Steatosis | Senior-Loken Syndrome | VACTERL/VATER Association | Epithelioid Hemangioma | Choroiditis | Epidermolysis Bullosa Simplex | Restrictive Dermopathy | Marinesco-Sjogren Syndrome | Binge Eating Disorder | Acute Myeloid Leukemia | Hepatic Veno-occlusive Disease | Niemann-Pick Disease, Type C | Scoliosis | Reflex Epilepsy | Dent Disease | Chronic Thromboembolic Pulmonary Hypertension | Chronic Myelomonocytic Leukemia | Trichomegaly | Gynecomastia | Traboulsi Syndrome | Esotropia | Shprintzen-Goldberg Syndrome | Recurrent Respiratory Papillomatosis | Alstrom Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Urticaria | Cancer, Skin | Schizencephaly | Rhabdomyosarcoma, Alveolar | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Congenital Nephrotic Syndrome | Congenital Afibrinogenemia | Hoyeraal-Hreidarsson Syndrome | Craniolenticulosutural Dysplasia | Pheochromocytoma | Tularemia | Glomerulonephritis | Sensorineural Hearing Loss | Leishmaniasis, Cutaneous | Episodic Ataxia Type 2 | Early Infantile Epileptic Encephalopathy 1 | Endometriosis | Cholera | Thymoma, Malignant | Cryptosporidiosis | Menkes Disease | Angiosarcoma | Connective Tissue Disorders | Coronary Artery Disease | Hypopigmentation | Leukoplakia, Oral | Hyperprolactinemia | Dysferlinopathy | Lactose Intolerance | Pituitary Dwarfism | Imerslund-Grasbeck Syndrome | Vulvovaginitis | Leukoplakia | Amish Infantile Epilepsy Syndrome | Osteoporosis-pseudoglioma Syndrome | Creatine Deficiency Syndrome