Disease

Type 0 Muscle Glycogen Storage Disease, GSD

About the Disease
Glycogen Storage Disease 0, Muscle, also known as glycogen storage disease due to muscle and heart glycogen synthase deficiency, is related to glycogen storage disease 0, liver and cardiac arrest. An important gene associated with Glycogen Storage Disease 0, Muscle is GYS1 (Glycogen Synthase 1). Affiliated tissues include heart, liver and skin, and related phenotypes are left ventricular hypertrophy and stroke

Common Targets
GYS1 | GYG1

疾病靶点研报
Type 0 Muscle Glycogen Storage Disease, GSD

Note: If you'd like to get a target analysis report for Type 0 Muscle Glycogen Storage Disease, GSD, 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 Type 0 Muscle Glycogen Storage Disease, GSD at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Melanoma | Lymphedema-distichiasis Syndrome | Spondylosis | Myelodysplasia | Juvenile Myoclonic Epilepsy | Cataplexy | Smoldering Myeloma | Hyperinsulinism-hyperammonemia Syndrome | Sarcoma, Endometrial Stromal | Dermatofibrosarcoma | Nemaline Myopathy 10 | Porphyria Cutanea Tarda | Common Variable Immunodeficiency | Kindler Syndrome | Yellow Fever | Brenner Tumor | Ectodermal Dysplasia | Hypokalemia | NGLY1 Deficiency | Poretti-Boltshauser Syndrome | Hyperthyroidism | Vitiligo | Cystitis, Interstitial | Craniolenticulosutural Dysplasia | Fibromuscular Dysplasia | Hypermetropia | Constipation | Glucagonoma | Glutaric Aciduria Type 3 | Creutzfeldt-Jakob Disease | Hypersensitivity | Progressive Familial Intrahepatic Cholestasis Type 3 | Sensorineural Hearing Loss | Babesiosis | Pityriasis Rubra Pilaris | Transthyretin-related Amyloidosis | Agranulocytosis | Globozoospermia | Familial Thoracic Aortic Aneurysm | Lennox-Gastaut Syndrome | Primary Biliary Cholangitis | Alkaptonuria | Pendred Syndrome | Cardiac Sarcoidosis | Unverricht-Lundborg Syndrome | Thymoma, Malignant | Hydronephrosis | Familial Hypobetalipoproteinemia | Neuroblastoma | Fuchs Dystrophy | Melnick-Needles Syndrome | Hypereosinophilic Syndrome | Scleritis | Cat Eye Syndrome | Emery-Dreifuss Muscular Dystrophy | Congenital Hemolytic Anemia | Glutaric Aciduria Type 2 | Benign Recurrent Intrahepatic Cholestasis 1 | Tyrosine Hydroxylase Deficiency | Double Outlet Right Ventricle | Hoyeraal-Hreidarsson Syndrome | Pneumococcal Meningitis | Spinocerebellar Ataxia Type 10 | Arterial Tortuosity Syndrome | POEMS Syndrome | Long QT Syndrome Type 2 | Congenital Aniridia | Nail Disorder, Nonsyndromic Congenital | Microphthalmia | Juvenile Myelomonocytic Leukemia | Ornithine Transcarbamylase Deficiency | Autoimmune Hemolytic Anemia | Conjunctivitis, Allergic | Rhabdomyosarcoma, Embryonal | Lung Diseases | Multifocal Motor Neuropathy | Nemaline Myopathy 8 | Duane Retraction Syndrome | Gestational Trophoblastic Disease | Chromosome 8q21.11 Deletion Syndrome | Colon Adenoma | Bardet-Biedl Syndrome | Crisponi Syndrome | Lymphoma, AIDS-related | Dengue Shock Syndrome | Diabetes Gestational | Sleep Apnea, Central | Benign Familial Pemphigus | Sarcoidosis, Pulmonary | Genitopatellar Syndrome | Combined Deficiency Of Factor V And Factor VIII | Pachyonychia Congenita | Takotsubo Cardiomyopathy | Cutaneous Angiosarcoma | Vertebrobasilar Insufficiency | Pyloric Stenosis, Infantile Hypertrophic | Eating Disorder | Craniosynostosis | Spinocerebellar Ataxia Type 1 | Guttate Psoriasis | Multiple Sclerosis, Relapsing-remitting | Vitamin A Deficiency | Papillon-Lefevre Syndrome | Atelosteogenesis Type 2 | Glycogen Storage Disease Type 4 | Cholelithiasis | Congenital Dysfibrinogenemia | Burn-McKeown Syndrome | Hyperglycemia | Pyelonephritis | Lipid Storage Myopathy | Zimmermann-Laband Syndrome | Schizophrenia, Paranoid | Rolandic Epilepsy | Haim-Munk Syndrome | Usher Syndrome Type I | IMAGe Syndrome | Hepatitis A | Hemophilia | Restrictive Dermopathy | Leishmaniasis, Cutaneous | Non-proliferative Diabetic Retinopathy | Insulinoma | Snyder-Robinson Syndrome | Dystonia Musculorum Deformans | Schizophrenia | Papilloma | Retinal Degeneration | Ectrodactyly | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Sialoadenitis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Odonto-onycho-dermal Dysplasia | Lipid Metabolism Disorders | Temtamy Preaxial Brachydactyly Syndrome | Congenital Ichthyosiform Erythroderma | Retinal Diseases | Language Disorders | Zellweger Syndrome | Bone Giant Cell Tumor | Adams-Oliver Syndrome | Li-Fraumeni Syndrome | Familial Hemiplegic Migraine | Agammaglobulinemia | Spinocerebellar Ataxia Type 21 | Lipid Storage Diseases | Charcot-Marie-Tooth Disease Type 3 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Wieacker-Wolff Syndrome | Panuveitis | Lassa Fever | Spinocerebellar Ataxia Type 31 | Cryopyrin-associated Periodic Syndromes | Blepharoconjunctivitis | Traboulsi Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Atrial Septal Defect | Tinea | Ichthyosis Bullosa Of Siemens | Homocystinuria | Mucolipidosis Type II | Thalassemia, Beta | Bulimia Nervosa | Dementia, Vascular | Cirrhosis | Cannabis Abuse | Zollinger-Ellison Syndrome | Lafora Disease | Metanephric Adenoma | Gastritis | Carcinoma, Small Cell | Wiedemann-Steiner Syndrome | Coronary Artery Disease | Bicuspid Aortic Valve | Graves Disease | Schizotypal Personality Disorder | Spondylolisthesis | Pycnodysostosis | Varicocele | Liddle Syndrome | Spinocerebellar Ataxia Type 27 | Infertility, Male | Myoclonus-dystonia Syndrome | Corneal Dystrophy And Perceptive Deafness | Microtia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Pierre Robin Syndrome | Nance-Horan Syndrome | Graft-versus-host Disease | Early Infantile Epileptic Encephalopathy 13 | Thyroiditis | Erythema Multiforme | Polymyositis | Hypodontia | Roberts Syndrome | Liver Diseases | Okihiro Syndrome | Anovulation | Skin Fragility-woolly Hair Syndrome | Botulism | Diverticulitis | T-cell Prolymphocytic Leukemia | Larsen Syndrome | Urea Cycle Disorder | Microcephalic Primordial Dwarfism | Systemic Mastocytosis | Wilson's Disease | Waldenstrom Macroglobulinemia | Thanatophoric Dysplasia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Heart Block | Chordoid Glioma | Overactive Bladder | Porphyria, Variegate | Congenital Muscular Dystrophy | KBG Syndrome | FG Syndrome | Atopy | Optic Atrophy 2 | Corneal Dystrophies, Hereditary | Rhabdoid Tumor | Jalili Syndrome | Pancreatitis, Chronic | Metabolic Syndrome | Osteochondroma | Diabetic Macular Edema | Avian Influenza | Gynecomastia | Charcot-Marie-Tooth Disease Axonal Type 2N | Exfoliative Dermatitis | Uterine Leiomyoma | Vestibular Disease | Epilepsy Of Infancy With Migrating Focal Seizures | Monilethrix | Pyoderma Gangrenosum | Myofibrillar Myopathy | Pineoblastoma | Guillain-Barre Syndrome | Gastroschisis | Aicardi-Goutieres Syndrome | Pancreatitis | Histoplasmosis | Superficial Spreading Melanoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Microcephaly | Goiter | Dengue Hemorrhagic Fever | Tibial Muscular Dystrophy | Progressive Familial Intrahepatic Cholestasis | Lipodystrophy | Cabezas Syndrome | Spinocerebellar Ataxia Type 5 | Heroin Dependence | Phenylketonuria II | Congenital Bilateral Absence Of Vas Deferens | Nephrotic Syndrome | Glomerulonephritis, Membranoproliferative | Renal Tubular Dysgenesis | Sarcoidosis | Sensory Neuropathy | Hypertension, Essential | Aceruloplasminemia | Niemann-Pick Disease, Type C | Whipple's Disease | N-acetylglutamate Synthase Deficiency | Aneurysm, Thoracic Aortic | Vitreoretinal Degeneration, Snowflake Type | Genee-Wiedemann Syndrome | Syphilis | Fukuyama Congenital Muscular Dystrophy | Werner's Syndrome | Benign Familial Infantile Seizures | Encephalopathy, Ethylmalonic | Cri-du-chat Syndrome | Hyperphenylalaninemia | Basal Ganglia Cerebrovascular Disease | Hereditary Coproporphyria | Pituitary Stalk Interruption Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Aldosterone Deficiency | Fibrillation, Atrial | Leukoplakia, Oral | Hereditary Sensory And Autonomic Neuropathy | Lysosomal Acid Lipase Deficiency | Gangliosidosis, GM1 | Allergic Contact Dermatitis | Atrioventricular Septal Defect | Schindler Disease | Neurofibrosarcoma | Hereditary Multiple Exostoses | Sialidosis Type I | Phosphoglycerate Dehydrogenase Deficiency | Communication Disorders | Glanzmann Thrombasthenia | Muir-Torre Syndrome | Parkinsonism | Proximal Symphalangism | Postaxial Polydactyly | Myotonic Disorders | Acrodermatitis | Conduct Disorder | Melanoma, Uveal | D-2-Hydroxyglutaric Aciduria | Astrocytoma, Anaplastic | Hereditary Hemorrhagic Telangiectasia Type 2 | Plasma Cell Dyscrasia | Antley-Bixler Syndrome | Fetal Akinesia Deformation Sequence | Lamellar Ichthyosis | Cone Dystrophy | Pneumothorax | Lymphoma, B-cell | Early Infantile Epileptic Encephalopathy 28 | Rett Syndrome | Mixed Connective Tissue Disease | L-2-Hydroxyglutaric Aciduria | Amish Infantile Epilepsy Syndrome | Light Chain Amyloidosis | Leprosy | Nephrocalcinosis | Familial Hyperaldosteronism | Hereditary Sensory Neuropathy Type 1 | Hepatitis, Autoimmune | Spina Bifida | Infantile Nephropathic Cystinosis | Alstrom Syndrome | Acral Lentiginous Melanoma | Hodgkin Lymphoma | Chronic Periodontitis | Hypoproteinemia, Hypercatabolic | Spinocerebellar Ataxia Type 7 | Astigmatism | Waardenburg Syndrome Type 2 | Periodic Limb Movement Disorder | Dwarfism | Xeroderma Pigmentosum | Primrose Syndrome | Dyslipidemia | Schwannoma | Bipolar Disorder | Muckle-Wells Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Prediabetes | Glycogen Storage Disease Type 5 | Hyperparathyroidism, Primary | Hypothyroidism | Ischemia | Sporadic Hemiplegic Migraine | VACTERL/VATER Association | Meningococcal Infections | Vitamin K Deficiency | Osteoporosis-pseudoglioma Syndrome | Hepatitis B, Chronic | Diabetic Neuropathy | Albinism | Agnathia-Otocephaly Complex | Spinocerebellar Ataxia Type 12 | Primary Pigmented Nodular Adrenocortical Disease | Peeling Skin Syndrome Type B | Torticollis | Duodenal Atresia | Adenylosuccinate Lyase Deficiency | Meleda Disease | Migraine | Dental Caries | Oculocutaneous Albinism Type 2 | Antithrombin III Deficiency | Crouzon Syndrome With Acanthosis Nigricans | Splenomegaly | Aneurysm, Abdominal Aortic | Gangliosidosis | Progressive Familial Intrahepatic Cholestasis Type 1 | Juvenile Hyaline Fibromatosis | Behavioral Variant Of Frontotemporal Dementia | Echinococcosis | Hyperekplexia | Prolactinoma | Esotropia | Cardiomyopathy, Peripartum | Niemann-Pick Disease, Type A | Granular Corneal Dystrophy Type 1 | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Osteoporosis, Postmenopausal | Disseminated Intravascular Coagulation | Strabismus | Heavy Chain Disease | Endometrial Hyperplasia | Malignant Fibrous Histiocytoma | Erectile Dysfunction | Ligneous Conjunctivitis | Harlequin Ichthyosis | Vulvovaginitis | Metachondromatosis | Rosacea | Benign Hereditary Chorea | Kearns-Sayre Syndrome | Moyamoya Disease | Diabetes Insipidus, Neurogenic | Myocardial Infarction | Trichotillomania