Disease

Glycogen Storage Disease Type 4

About the Disease
Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency, also known as glycogen storage disease type iv, is related to glycogen storage disease iv and myopathy, and has symptoms including hepatosplenomegaly and muscle weakness. An important gene associated with Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency is GBE1 (1,4-Alpha-Glucan Branching Enzyme 1). The drug Pharmaceutical Solutions has been mentioned in the context of this disorder. Affiliated tissues include liver, skeletal muscle and heart, and related phenotypes are generalized abnormality of skin and abnormal muscle glycogen content

Common Targets
AGL | GBE1 | PYGL

疾病靶点研报
Glycogen Storage Disease Type 4

Note: If you'd like to get a target analysis report for Glycogen Storage Disease Type 4, 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 Glycogen Storage Disease Type 4 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Sponastrime Dysplasia | Sleep Disorder | Congenital Tufting Enteropathy | Keratitis | Tic Disorder | Cholelithiasis | Stickler Syndrome | Inflammatory Myofibroblastic Tumor | Congenital Mirror Movements | Senior-Loken Syndrome | Wolman Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Liddle Syndrome | Pseudo-pseudohypoparathyroidism | Protein C Deficiency | Infantile Refsum Disease | Benign Hereditary Chorea | Anencephaly | Peeling Skin Syndrome Type B | Pernicious Anemia | Chronic Neutrophilic Leukemia | Bronchiectasis | Hyperparathyroidism, Primary | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Dysgerminoma | Autonomic Nervous System Disorders | N-acetylglutamate Synthase Deficiency | Prader-Willi Syndrome | Epidermolysis Bullosa Dystrophica | Fibrosis | Impetigo | Hypospadias | Follicular Dendritic Cell Sarcoma | Motor Neuron Diseases | Auriculocondylar Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Early Infantile Epileptic Encephalopathy 1 | Hemorrhage | Gaucher Disease | Warsaw Breakage Syndrome | Sulfite Oxidase Deficiency | Hepatitis C, Chronic | Malaria, Cerebral | Achromatopsia | Splenomegaly | Aromatic L-amino Acid Decarboxylase Deficiency | Infertility | Wolff-Parkinson-White Syndrome | Choroideremia | Pancytopenia | Anorectal Malformations | Keratocystic Odontogenic Tumor | Hereditary Sensory Neuropathy Type 1 | L-2-Hydroxyglutaric Aciduria | Pyruvate Carboxylase Deficiency Disease | Alpha-1 Antitrypsin Deficiency | Herpes Genitalis | Angioedema, Hereditary | Rheumatic Heart Disease | Familial Partial Lipodystrophy | Pure Red Cell Aplasia | Cysticercosis | Acne | Ataxia-ocular Apraxia 2 | Hypodontia | Acute Coronary Syndrome | Trichothiodystrophy | Hepatitis A | Hernia, Inguinal | Cluster Headache | Adrenomyeloneuropathy | Silver-Russell Syndrome | Absence Epilepsy | Familial Mediterranean Fever | Anodontia | Neurocutaneous Melanocytosis | CEDNIK Syndrome | PHARC Syndrome | Scabies | Early Infantile Epileptic Encephalopathy | Campomelic Dysplasia | Withdrawal Syndrome | Lattice Corneal Dystrophy | Overactive Bladder | Cheilitis | Hyperparathyroidism-jaw Tumor Syndrome | Lentigo | Meier-Gorlin Syndrome | Hyperuricemia | Spinocerebellar Ataxia Type 28 | Meesmann Corneal Dystrophy | Cholangiocarcinoma | Allergic Contact Dermatitis | Congenital Myasthenic Syndrome | Pleurisy | Blepharophimosis Syndrome | Iron Metabolism Disorders | Barakat Syndrome | Cerebellar Ataxia, Cayman Type | Thyrotoxic Periodic Paralysis | Macular Corneal Dystrophy | Autoimmune Hemolytic Anemia | Proteasome-associated Autoinflammatory Syndrome 2 | Erythema Multiforme | Aneurysm, Abdominal Aortic | Restless Legs Syndrome | Juvenile Myoclonic Epilepsy | Charcot-Marie-Tooth Disease Type 2T | Congenital Adrenal Hyperplasia 1 | Phenylketonuria | Cystinosis | Pineoblastoma | Gray Platelet Syndrome | Oligodendroglioma | Myopathy | Influenza | DRESS Syndrome | Leukoplakia | Pituitary Dwarfism | Intracranial Hypertension | Greig Cephalopolysyndactyly Syndrome | Spinocerebellar Ataxia | Hemangioendothelioma | Silicosis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Vertebrobasilar Insufficiency | Dupuytren Disease | Congenital Hypofibrinogenemia | Hodgkin Lymphoma | Congenital Lipoid Adrenal Hyperplasia | Keratosis, Actinic | Prolymphocytic Leukemia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Hypereosinophilic Syndrome | Thyroid Dyshormonogenesis | VEXAS Syndrome | Dubin-Johnson Syndrome | Alstrom Syndrome | Meleda Disease | Dystonia-parkinsonism, X-linked | Pigment Dispersion Syndrome | Carotid Artery Disease | Hereditary Mixed Polyposis Syndrome | Orthostatic Intolerance | Oligospermia | Hypohidrotic Ectodermal Dysplasia | Sandhoff Disease | Autism Spectrum Disorders | Progressive External Ophthalmoplegia | Extramammary Paget's Disease | Thin Basement Membrane Disease | Meningeal Melanocytoma | Congenital Bilateral Absence Of Vas Deferens | Apraxia | Hypophosphatasia | Anorexia Nervosa | Hartnup Disease | Gingivitis | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Congestive Heart Failure | Glycogen Storage Disease Type 0 | Recurrent Respiratory Papillomatosis | Aceruloplasminemia | Choriocarcinoma | Hepatic Veno-occlusive Disease | Sick Sinus Syndrome | Norrie Disease | Hyperuricemic Nephropathy, Familial Juvenile | Diabetes | Chondroma | Generalized Epilepsy And Paroxysmal Dyskinesia | Graft-versus-host Disease | Osteonecrosis | Hypertension, Essential | Thalassemia | Down Syndrome | Ornithine Transcarbamylase Deficiency | Multiple System Atrophy | Liebenberg Syndrome | Hyperparathyroidism | Chorea | Perry Syndrome | Otitis Media | Saul-Wilson Syndrome | Ocular Surface Squamous Neoplasia | Erythematotelangiectatic Rosacea | Hemophilia | Hereditary Spastic Paraplegia | Carney-Stratakis Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Osteonecrosis Of The Jaw | Hamartoma | Hereditary Spherocytosis | Neuromyotonia | Distal Myopathy | Hepatitis, Autoimmune | Hypotrichosis | Pulmonary Alveolar Microlithiasis | Hypermetropia | Cardiomyopathy, Restrictive | Granular Corneal Dystrophy | Ganglioneuroma | Colitis, Collagenous | Hydrops Fetalis | Agammaglobulinemia | Varices | CHARGE Syndrome | Colitis, Microscopic | Neurofibromatosis | Niemann-Pick Disease | Empyema | Heart Block | Sarcomatoid Carcinoma Of The Lung | Nemaline Myopathy | Hemochromatosis | Rhabdomyosarcoma, Embryonal | Non-Langerhans Cell Histiocytosis | Progressive Myoclonic Epilepsy | Lichen Planus | Becker Muscular Dystrophy | High Molecular Weight Kininogen Deficiency | Retinoschisis | Aicardi-Goutieres Syndrome | Alveolar Capillary Dysplasia | Myopia | Asthma, Exercise-induced | Fetal Alcohol Syndrome | Neurofibrosarcoma | Alopecia Totalis | Stroke | Encephalitis | Thanatophoric Dysplasia | Diastrophic Dysplasia | Dementia | Osteochondroma | Charcot-Marie-Tooth Disease Type 2D | Peroxisomal Disorder | McKusick Type Metaphyseal Chondrodysplasia | Astigmatism | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Tendinopathy | Sclerosing Cholangitis | Gestational Trophoblastic Disease | Benign Familial Infantile Seizures | Hemangioblastoma | Sialoadenitis | Lymphoma, AIDS-related | Behavioral Variant Of Frontotemporal Dementia | Danon Disease | Hypervalinemia | Epidermolytic Hyperkeratosis | Nevus | Calcium Pyrophosphate Deposition Disease | Ectrodactyly | Neonatal Progeroid Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Moyamoya Disease | Infantile Neuroaxonal Dystrophy | Nephropathy | Carcinoid Tumor | Common Variable Immunodeficiency | Gnathodiaphyseal Dysplasia | Acute Motor Axonal Neuropathy | Infectious Diarrhea | Neurotoxicity | FG Syndrome | Giant Cell Arteritis | Toxic Epidermal Necrolysis | Fahr Disease | T-cell Prolymphocytic Leukemia | Epidermolytic Ichthyosis, Annular | Hydronephrosis | Ureteropelvic Junction Obstruction | Autosomal Recessive Congenital Ichthyosis | Neuromyelitis Optica | Muckle-Wells Syndrome | Growth Hormone Excess | Spondyloarthritis | Hyperacusis | Stargardt Disease | Nephronophthisis | Ebstein Anomaly | Ghosal Syndrome | Periventricular Leukomalacia | Porphyria | C3 Glomerulopathy | Lymphoma, Mantle Cell | Antisocial Personality Disorder | Pyoderma Gangrenosum | Spinocerebellar Ataxia Type 3 | McCune-Albright Syndrome | Chronic Granulomatous Disease, X-linked | Oligoastrocytoma | Nephrocalcinosis | Long QT Syndrome Type 3 | Scapuloperoneal Myopathy, X-linked Dominant | Bartsocas-Papas Syndrome | Hydrolethalus Syndrome | Optic Neuritis | Liver Failure, Acute Infantile | Tumoral Calcinosis | Cantu Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Glomerulonephritis | Klinefelter Syndrome | Hyperlipidemia Type V | Emery-Dreifuss Muscular Dystrophy | Wolfram Syndrome 2 | Autoimmune Polyendocrinopathy Syndrome Type I | Kernicterus | Pain | Cohen Syndrome | Giant Axonal Neuropathy | Histiocytic Sarcoma | NGLY1 Deficiency | Leukoplakia, Oral | Hypotension, Orthostatic | Veno-occlusive Disease | GNE Myopathy | Autoimmune Disease | Waardenburg Syndrome Type 2A | Conn Syndrome | Familial Hypertrophic Cardiomyopathy | Arteriovenous Malformations | AIDS | Hennekam Lymphangiectasia-lymphedema Syndrome | Hereditary Xerocytosis | Pseudohypoparathyroidism Type 1A | Heart Failure | Otitis Externa | Molybdenum Cofactor Deficiency | Multiple Hamartoma Syndrome | Sitosterolemia | Chronic Kidney Disease | Spondylometaphyseal Dysplasia | Hypokalemia | Motion Sickness | Retinal Dystrophy | Syndactyly | Purpura | Myosin Storage Myopathy | Granuloma Annulare | Hyperlipidemia, Familial Combined | Sepiapterin Reductase Deficiency | Atelosteogenesis Type 2 | Vasculitis | Vici Syndrome | Atelosteogenesis Type 1 | Duane Retraction Syndrome | Polymicrogyria | Scleroderma, Diffuse | Vitreoretinal Degeneration, Snowflake Type | Niemann-Pick Disease, Type B | Sleep Apnea | Osteogenesis Imperfecta Type V | Parkinson Disease 6, Autosomal Recessive Early-onset | Histoplasmosis | Waldenstrom Macroglobulinemia | Renpenning Syndrome | Cabezas Syndrome | Hydrocephalus | Pleomorphic Xanthoastrocytoma | Reflex Epilepsy | Epidermal Nevus Syndrome | Glycogen Storage Disease Type 1a | Niemann-Pick Disease, Type C | Neuromuscular Disorders | Raine Syndrome | C3 Glomerulonephritis | Charcot-Marie-Tooth Disease Type 4D | Retinal Telangiectasia | Usher Syndrome Type I | Fundus Albipunctatus | Schizencephaly | Hashimoto Thyroiditis | Aplasia Cutis Congenita | Stomatitis | H Syndrome | Autism | Microtia | Galactosemia | Myasthenia | Erythromelalgia | Spinocerebellar Ataxia Type 13 | Acute Anterior Uveitis | Acanthosis Nigricans | Intermittent Explosive Disorder | Pneumoconiosis | Asthma | Isovaleric Acidemia | Tetanus | Rolandic Epilepsy | Leishmaniasis, Visceral | Lymphomatoid Granulomatosis | Chondromyxoid Fibroma | Episodic Ataxia | Multiple Sclerosis, Primary Progressive | LEOPARD Syndrome | Cerebral Cavernous Malformations | Osteoporosis