Myoclonic Atonic Epilepsy

About the Disease
Epilepsy with Myoclonic-Atonic Seizures, also known as myoclonic astatic epilepsy, is related to photosensitive epilepsy and sturge-weber syndrome. An important gene associated with Epilepsy with Myoclonic-Atonic Seizures is SCN1A (Sodium Voltage-Gated Channel Alpha Subunit 1), and among its related pathways/superpathways are Fragile X syndrome and Rett syndrome causing genes. The drugs Cannabidiol and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include brain, skin and bone, and related phenotypes are eeg with focal spike waves and generalized myoclonic-atonic seizure

Common Targets
CACNA1H | SUN1 | MECP2 | CHD2 | KCNT1 | KLC2 | SHROOM4 | KCNA2 | STXBP1

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

Other Diseases

Congenital Lipoid Adrenal Hyperplasia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Autoimmune Polyendocrinopathy Syndrome Type I | Congenital Dyserythropoietic Anemia Type 1 | Fanconi Anemia | Lesch-Nyhan Syndrome | Glycogen Storage Disease | Keratoconjunctivitis | Tic Disorder | Cataract | Hyperuricemia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Diastrophic Dysplasia | Pneumoconiosis | Cutaneous Lupus Erythematosus | Nail Disorder, Nonsyndromic Congenital | Cenani-Lenz Syndactyly Syndrome | Malonyl-CoA Decarboxylase Deficiency | Infertility, Male | Hypersensitivity Pneumonitis | Hyperkalemic Periodic Paralysis | Viral Meningitis | Diverticulitis | Adenylosuccinate Lyase Deficiency | Heavy Chain Disease | Giant Axonal Neuropathy | Walker-Warburg Syndrome | Blomstrand Osteochondrodysplasia | Pigment Dispersion Syndrome | Meniere's Disease | Trichothiodystrophy | Cervicitis | Neurofibromatosis Type 2 | Dysplastic Nevus | Becker Muscular Dystrophy | Multicystic Renal Dysplasia | Cholecystitis | Supravalvular Aortic Stenosis | Atopy | Mitochondrial Encephalomyopathy | Wieacker-Wolff Syndrome | Avian Influenza | Frontometaphyseal Dysplasia | Homocystinuria | Sepiapterin Reductase Deficiency | L-2-Hydroxyglutaric Aciduria | Congenital Absence Of Vas Deferens | Periventricular Leukomalacia | McLeod Syndrome | Diabetic Encephalopathy | Methylmalonic Aciduria And Homocystinuria, CblC Type | Cherubism | Bruck Syndrome | Hypophosphatasia | Placenta Previa | Glycogen Storage Disease Type 1b | Urolithiasis | Microcephaly, Seizures, And Developmental Delay | Purpura | Maternally Inherited Diabetes And Deafness | Spinal And Bulbar Muscular Atrophy | Trichotillomania | Xeroderma Pigmentosum | Retinal Vasculitis | Gastroenteritis | Hyperferritinemia-cataract Syndrome | Papilloma | CEDNIK Syndrome | Huntington's Disease | Lichen Sclerosus | Tyrosinemia | Filariasis | Renal Tubular Acidosis | Superficial Spreading Melanoma | Overactive Bladder | Chronic Lymphocytic Leukemia | Tetraplegia | Tylosis With Esophageal Cancer | Crisponi Syndrome | Bipolar Disorder | Fowler's Syndrome | Rheumatoid Arthritis | Senior-Loken Syndrome | Gastric Atrophy | Usher Syndrome Type IIC | Scoliosis | Bone Marrow Necrosis | 3-hydroxy-3-methylglutaric Aciduria | Pterygium | Pseudoachondroplasia | Prune Belly Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Lassa Fever | Chylothorax, Congenital | Hypercholesterolemia, Familial | Hypopituitarism | Glomerulonephritis | Cerebrotendinous Xanthomatosis | Tibial Muscular Dystrophy | Cardiospondylocarpofacial Syndrome | Carney Triad | Van Der Knaap Disease | Metachromatic Leukodystrophy | Pachyonychia Congenita | Discoid Lupus Erythematosus | DICER1 Syndrome | Hepatitis A | Cohen Syndrome | Mabry Syndrome | Trichuriasis | Monilethrix | Pyelonephritis | Wilson's Disease | Hypolipoproteinemia | Chromosome 9q34.3 Deletion Syndrome | Smith-Lemli-Opitz Syndrome | Hemorrhage | Galloway-Mowat Syndrome | Nager Acrofacial Dysostosis | Chronic Idiopathic Myelofibrosis | Seborrheic Dermatitis | Liver Failure, Acute Infantile | Prolactinoma | Gallstones | Tracheal Disorders | Charcot-Marie-Tooth Disease Type 2D | Pneumococcal Meningitis | Cluster Headache | Learning Disability | Triple A Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Astrocytoma | Thin Basement Membrane Disease | DEND Syndrome | Transthyretin-related Amyloidosis | Dwarfism | CDKL5 Deficiency Disorder | Pitt-Hopkins Syndrome | High Molecular Weight Kininogen Deficiency | Acute Coronary Syndrome | Neuroectodermal Tumors, Primitive | Pierpont Syndrome | Gastrointestinal Disorders | Retinitis Pigmentosa 3 | Common Cold | DNA Ligase IV Deficiency | Hypersomnia | Macrodactyly | Arthritis, Reactive | Lymphoma, Mantle Cell | Encephalopathy, Hepatic | Hyperglycemia | Pulmonary Veno-occlusive Disease | Aicardi-Goutieres Syndrome | Hemorrhoids | Microphthalmia | Hypervalinemia | HANAC Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Congenital Hemolytic Anemia | Bartter Syndrome | Barrett Esophagus | Congenital Stromal Corneal Dystrophy | Myelomeningocele | Apraxia | Progressive Familial Intrahepatic Cholestasis | Vitreoretinal Degeneration, Snowflake Type | Hermansky-Pudlak Syndrome | LMNA-related Congenital Muscular Dystrophy | Paternal Uniparental Disomy Of Chromosome 14 | Alpha-thalassemia Myelodysplasia Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Behavioral Variant Of Frontotemporal Dementia | Early Infantile Epileptic Encephalopathy 13 | Chronic Beryllium Disease | Scleritis | WAGR Syndrome | Pancytopenia | Vitreoretinopathy, Proliferative | Glutaric Aciduria Type 2 | Plasmacytoma | Familial Hemiplegic Migraine | Amenorrhea | Lupus Erythematosus | Relapsing Polychondritis | Hepatic Veno-occlusive Disease | Erythematotelangiectatic Rosacea | Pancreatitis, Chronic | Acute Leukemia | Spinocerebellar Ataxia Type 10 | Cri-du-chat Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Progressive Myoclonic Epilepsy | Usher Syndrome | Emery-Dreifuss Muscular Dystrophy | Liebenberg Syndrome | Endometrial Hyperplasia | Vascular Calcification | Jalili Syndrome | Infantile Spasm | Chronic Mucocutaneous Candidiasis | Congenital Mirror Movements | Urticaria | Hyperinsulinemia | Chronic Enteropathy Associated With SLCO2A1 Gene | Celiac Disease | Glioma | Early Infantile Epileptic Encephalopathy 4 | Dementia, Vascular | Glycogen Storage Disease Type 5 | Multiple Epiphyseal Dysplasia | Specific Granule Deficiency | Corneal Neovascularization | Mixed Connective Tissue Disease | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | HUPRA Syndrome | Neurofibromatosis | Spondylocarpotarsal Synostosis Syndrome | Parvovirus B19 Infection | Macular Degeneration | Lissencephaly 2 | Intestinal Obstruction | Myocardial Infarction | Ophthalmia, Sympathetic | Coenzyme Q10 Deficiency | Cerebellofaciodental Syndrome | Fibrosarcoma | Lymphoproliferative Disorders | Congenital Hereditary Endothelial Dystrophy Type I | Carcinoma, Small Cell | Spinocerebellar Ataxia Type 20 | Diffuse Palmoplantar Keratoderma | 3-M Syndrome | Retinal Dystrophy | Renal Oncocytoma | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Primary Carnitine Deficiency | Fibromuscular Dysplasia | Anorectal Malformations | Transient Bullous Dermolysis Of The Newborn | Von Willebrand Disease | Plasma Cell Leukemia | Myoclonic Epilepsy With Ragged Red Fibers | Noonan Syndrome | Epidermolysis Bullosa Simplex, Generalized | Sialoadenitis | Erythromelalgia | Costello Syndrome | Macrophage Activation Syndrome | Spermatocele | Congenital Disorders Of Glycosylation Type II | Intellectual Disability, Autosomal Dominant 5 | Lactose Intolerance | Diabetes Type 1 | Goldenhar Syndrome | Vaginitis | Sclerocornea | Meningeal Melanocytoma | Esophagitis, Eosinophilic | Glutaric Aciduria Type 1 | Anuria | Cone Dystrophy | Basal Cell Nevus Syndrome | Rhabdoid Tumor | Autosomal Recessive Congenital Ichthyosis | Crouzon Syndrome With Acanthosis Nigricans | Diabetes Insipidus | Sengers Syndrome | Uterine Leiomyoma | Hemochromatosis Type 1 | Systemic Mastocytosis | Holoprosencephaly | Colitis, Microscopic | Palmoplantar Keratoderma | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Diabetes Gestational | Spinocerebellar Ataxia Type 2 | Acute Myeloid Leukemia | Takenouchi-Kosaki Syndrome | Benign Hereditary Chorea | Asphyxia Neonatorum | Optic Neuritis | Allan-Herndon-Dudley Syndrome | Methemoglobinemia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Skin Papilloma | Hemochromatosis Type 2 | Glaucoma | Acute Kidney Injury | Diffuse Intrinsic Pontine Glioma | Panniculitis | Down Syndrome | CREST Syndrome | Renal Hypouricemia | Shock, Cardiogenic | Agammaglobulinemia | Thromboembolism | Neonatal Progeroid Syndrome | Thyrotoxic Periodic Paralysis | Language Disorders | Polyarteritis Nodosa | Primary Lateral Sclerosis | Wolfram Syndrome 2 | Gastroschisis | Meier-Gorlin Syndrome | Cystitis | Waardenburg Syndrome Type 2A | Epidermolysis Bullosa Simplex, Localized | Erythema Multiforme | Nemaline Myopathy 10 | IgA Nephropathy | Saul-Wilson Syndrome | Juvenile Myelomonocytic Leukemia | Persistent Mullerian Duct Syndrome | Stiff-man Syndrome | Epicondylitis | Basal Ganglia Disease, Biotin-responsive | Microcephalic Primordial Dwarfism | Hypogonadism | Congenital Torticollis | Spinocerebellar Ataxia Type 38 | Hyperuricemic Nephropathy, Familial Juvenile | GAPO Syndrome | Focal Cortical Dysplasia Type 2 | Arterial Tortuosity Syndrome | Hyperlipidemia, Familial Combined | Epidermolytic Ichthyosis, Annular | Prostatitis | Fatty Aldehyde Dehydrogenase Deficiency | Glycogen Storage Disease Type 1 | Adams-Oliver Syndrome | Hepatoblastoma | Feingold Syndrome | Scleroderma | Idiopathic Pulmonary Fibrosis | Vitamin B12 Deficiency | Pseudohypoaldosteronism | Hemangioma | Blastomycosis | Glutathione Synthetase Deficiency | Spondyloarthritis | Neuroendocrine Cancer | Congenital Central Hypoventilation Syndrome | Tardive Dyskinesia | Heterotopic Ossification | Best Macular Dystrophy | Rosacea | Strabismus | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Wolfram Syndrome | Systemic Lupus Erythematosus | Schnitzler Syndrome | Heart Septal Defects | Goiter, Nodular | Craniopharyngioma | Sialidosis | Usher Syndrome Type I | Carcinoma In Situ | Charcot-Marie-Tooth Disease, Type 2 | Basal Ganglia Cerebrovascular Disease | Juvenile Hyaline Fibromatosis | Alkaptonuria | Methemoglobinemia Type IV | Peutz-Jeghers Syndrome | Tietze Syndrome | Guttate Psoriasis | Farber Disease | Episodic Ataxia Type 2 | Schwannomatosis | Benign Familial Infantile Seizures | Dental Caries | Spinocerebellar Ataxia Type 6 | Leber Congenital Amaurosis | Harlequin Ichthyosis | Pyoderma Gangrenosum | Aromatic L-amino Acid Decarboxylase Deficiency | Gerodermia Osteodysplastica | Myasthenia | Klippel-Feil Syndrome | C3 Glomerulonephritis | Chondrodysplasia Punctata 2, X-linked Dominant | Roberts Syndrome | Hyperekplexia | Agranulocytosis | DOCK8 Immunodeficiency Syndrome | Sick Sinus Syndrome 1 | Ocular Surface Squamous Neoplasia | Carbonic Anhydrase VA Deficiency | Syphilis | Xeroderma Pigmentosum Variant Type | Frank-ter Haar Syndrome | Acanthosis Nigricans | Glycogen Storage Disease Type 1a | Blue Rubber Bleb Nevus Syndrome | Duodenal Atresia | Cutaneous Angiosarcoma | Limb Girdle Muscular Dystrophy | Sclerosteosis 2 | Waldenstrom Macroglobulinemia | Evans Syndrome