Oculopharyngeal Muscular Dystrophy

About the Disease
Oculopharyngeal Muscular Dystrophy, also known as muscular dystrophy, oculopharyngeal, is related to muscular dystrophy and myopathy, and has symptoms including facial paresis An important gene associated with Oculopharyngeal Muscular Dystrophy is PABPN1 (Poly(A) Binding Protein Nuclear 1), and among its related pathways/superpathways are Processing of Capped Intron-Containing Pre-mRNA and Translational Control. Affiliated tissues include eye, tongue and lung, and related phenotypes are ptosis and myopathy

Common Targets
HNRNPA2B1 | Chaperone (nonspecified subtype) | NRL | LRP12 | PABPN1

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

Other Diseases

Ependymoma | Alopecia Totalis | CREST Syndrome | Hypercalcemia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Porphyria, Variegate | Sleep Disorder | Neurotoxicity | Keratitis | Pemphigus | Dystonia | Heroin Dependence | Neuroectodermal Tumors, Primitive | Spinocerebellar Ataxia Type 12 | Bardet-Biedl Syndrome | Erythropoietic Protoporphyria | Tremor | Wagner Disease | Carcinoma, Signet Ring Cell | Wiedemann-Steiner Syndrome | Hydrocephalus, Normal Pressure | Werner's Syndrome | Cutaneous T-cell Lymphoma | Thrombosis | Carney Triad | Frank-ter Haar Syndrome | Familial Retinal Arterial Macroaneurysm | Fascioliasis | Migraine | Veno-occlusive Disease | Stevens-Johnson Syndrome | Granular Corneal Dystrophy Type 1 | Papulopustular Rosacea | Usher Syndrome Type II | Marinesco-Sjogren Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Guillain-Barre Syndrome | Charcot-Marie-Tooth Disease Type 2E | Vitamin A Deficiency | Encephalopathy, Ethylmalonic | Usher Syndrome Type I | Cerebral Amyloid Angiopathy | Tetanus | Castleman Disease | Crohn's Disease | Sturge-Weber Syndrome | Lymphoma, Mantle Cell | Bruck Syndrome | Congenital Primary Aphakia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Anxiety Disorders | Chorea-acanthocytosis | Hypertensive Nephropathy | Thanatophoric Dysplasia | Patent Foramen Ovale | Tricho-hepato-enteric Syndrome | Fetal Alcohol Syndrome | Charcot-Marie-Tooth Disease Type 2D | Ornithine Transcarbamylase Deficiency | Omenn Syndrome | Hypokalemic Periodic Paralysis | Alpers Syndrome | Corneal Dystrophy | Niemann-Pick Disease | Retinopathy Of Prematurity | Primary Aldosteronism | Pseudohypoparathyroidism Type 1A | Blood Protein Disorders | Carney-Stratakis Syndrome | Fanconi Syndrome | Von Willebrand Disease | Ellis-Van Creveld Syndrome | Chromosome 17q21.31 Deletion Syndrome | Shock, Cardiogenic | Hypermethioninemia | Retinoschisis | Pleomorphic Xanthoastrocytoma | Meconium Ileus | Oligodendroglioma | Cardiac Arrest | Autism | Seizures | Fucosidosis | Congenital Disorders Of Glycosylation Type II | Cholecystitis | Cone Dystrophy | Sporadic Inclusion Body Myositis | Myotonia | Hereditary Inclusion Body Myopathy | Trichomegaly | Periventricular Leukomalacia | Fragile X Syndrome | Myositis, Focal | Progressive Familial Intrahepatic Cholestasis Type 2 | Sulfite Oxidase Deficiency | Congenital Dysfibrinogenemia | Split Hand-foot Malformation | Myelitis, Transverse | Megaloblastic Anemia | Chromosome 8q21.11 Deletion Syndrome | Glioblastoma | Macular Corneal Dystrophy | Kabuki Syndrome 2 | Fowler's Syndrome | Keratosis | Orthostatic Intolerance | Leukocyte Adhesion Deficiency Type 1 | Pituitary Stalk Interruption Syndrome | Hypertension, Pulmonary | Rhabdomyosarcoma, Alveolar | Aneurysm, Abdominal Aortic | Hyperparathyroidism, Primary | Ichthyosis | Giant Cell Arteritis | Chitayat Syndrome | Craniometaphyseal Dysplasia | Persistent Truncus Arteriosus | Myelofibrosis | Zollinger-Ellison Syndrome | Hyperkeratosis | Kallmann Syndrome | Metabolic Syndrome | Polycystic Kidney, Autosomal Dominant | Intestinal Tuberculosis | Huntington's Disease-like 2 | Hereditary Sensory And Autonomic Neuropathy | Otosclerosis | Hepatitis C, Chronic | Autosomal Recessive Congenital Ichthyosis | Prolactinoma | Angelman Syndrome | Dysfibrinogenemia | Wolman Disease | Hemangioblastoma | Fabry's Disease | Esophageal Adenocarcinoma | Pseudohypoparathyroidism Type 1C | Herpes Simplex Dermatitis | Charcot-Marie-Tooth Disease, Type 6 | Acrodermatitis | Dwarfism | Vitamin B12 Deficiency | Gastroenteritis | Renal Tubular Acidosis | Epiphyseal Chondrodysplasia, Miura Type | Androgen Insensitivity | Chronic Beryllium Disease | Cardiomyopathy, Peripartum | Familial Glucocorticoid Deficiency | Gnathodiaphyseal Dysplasia | X-linked Charcot-Marie-Tooth Disease | Sleep Apnea, Obstructive | Spasticity | Cohen Syndrome | Pierre Robin Syndrome | Chronic Granulomatous Disease, X-linked | Angioedema, Acquired | Tendinopathy | Cushing Syndrome | Rett Syndrome | Metachromatic Leukodystrophy | Leiomyosarcoma | Beckwith-Wiedemann Syndrome | Tyrosine Hydroxylase Deficiency | Premature Ejaculation | Hyperparathyroidism | Osteogenesis Imperfecta Type IV | Seborrheic Dermatitis | Eiken Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hemoglobinopathies | Cutaneous Angiosarcoma | Hyperhomocysteinemia | Hemochromatosis Type 2 | Nicotine Addiction | Erythrokeratodermia Variabilis | Open-angle Glaucoma | Rothmund-Thomson Syndrome | Anterior Segment Dysgenesis | Avian Influenza | Li-Fraumeni Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Uveitis, Anterior | Arthritis, Reactive | Pitt-Hopkins Syndrome | Hyperinsulinemic Hypoglycemia | Beare-Stevenson Syndrome | Asplenia | Carcinoma, Transitional Cell | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Tinea Versicolor | Uveitis | Hidradenitis Suppurativa | Hypotension, Orthostatic | Heavy Chain Disease | Arteriovenous Malformations | Synovitis | Alazami Syndrome | Neuronal Ceroid Lipofuscinosis | Chorioretinitis | Rhinitis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Spina Bifida | Adenocarcinoma | Sclerosing Cholangitis | Arthritis | Osteogenesis Imperfecta Type III | Systemic Lupus Erythematosus | Lissencephaly 2 | Fuchs Heterochromic Iridocyclitis | Lipid Metabolism Disorders | Erectile Dysfunction | Peroxisomal Disorder | Cystitis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Progressive Familial Intrahepatic Cholestasis Type 1 | Diverticulitis | GLUT1 Deficiency Syndrome | Bloom Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Colitis, Lymphocytic | Reye Syndrome | Paget's Disease Of The Breast | Filariasis | Adenoid Cystic Carcinoma | Supravalvular Aortic Stenosis | Multiple Epiphyseal Dysplasia | Congenital Dyserythropoietic Anemia | Microcephaly | Meckel-Gruber Syndrome | Constipation | Epidermolysis Bullosa Simplex, Generalized | Albinism | Cabezas Syndrome | Crigler-Najjar Syndrome | Primary Torsion Dystonia | Depression | Pseudoachondroplasia | Wiskott-Aldrich Syndrome | Congenital Bilateral Absence Of Vas Deferens | Nail-Patella Syndrome | Crisponi Syndrome | Neurofibromatosis Type 2 | Pneumonia, Viral | Familial Dysautonomia | Proteasome-associated Autoinflammatory Syndrome 2 | Glaucomatocyclitic Crisis | Congenital Lipoid Adrenal Hyperplasia | Ocular Albinism Type 1 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Adrenoleukodystrophy, X-linked | Genitopatellar Syndrome | Pseudohypoparathyroidism Type 1B | Cervical Dystonia | Acanthosis Nigricans | Alpha-mannosidosis | Menetrier Disease | Actinomycetoma | Syncope | Rubinstein-Taybi Syndrome | Angiosarcoma | Ganglioneuroma | Infantile Neuroaxonal Dystrophy | Microtia | Antisynthetase Syndrome | Myosin Storage Myopathy | Purpura | Metanephric Adenoma | Neutrophilia | Cornelia De Lange Syndrome | Congestive Heart Failure | Chromosome 9q34.3 Deletion Syndrome | Brugada Syndrome 1 | Pseudomyxoma Peritonei | Bipolar Disorder | Anorchia | Meniere's Disease | Congenital Adrenal Hyperplasia | DiGeorge Syndrome | Thalassemia | Giant Axonal Neuropathy | Oculocutaneous Albinism Type 1 | Hypophosphatasia | Hennekam Lymphangiectasia-lymphedema Syndrome | Cannabis Abuse | Distal Spinal Muscular Atrophy | Glaucoma | Agnathia-Otocephaly Complex | Spinocerebellar Ataxia Type 42 | Botulism | Myopia | Senior-Loken Syndrome | Trichotillomania | Retinoblastoma | Hypopituitarism | Cholangitis | Pontocerebellar Hypoplasia | Necrobiosis Lipoidica | Mucolipidosis | Bernard-Soulier Syndrome | Hyperkalemic Periodic Paralysis | Cenani-Lenz Syndactyly Syndrome | Nestor-Guillermo Progeria Syndrome | Pure Autonomic Failure | Zimmermann-Laband Syndrome | Hashimoto Thyroiditis | Cold-induced Sweating Syndrome | Glutaric Aciduria Type 3 | Porencephaly | Osteosarcoma | Micro Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Pontocerebellar Hypoplasia Type 2 | Congenital Myopathy | Congenital Hereditary Endothelial Dystrophy Type II | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Creatine Deficiency Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Waardenburg Syndrome Type 4 | Lymphoproliferative Disease, X-linked | Chronic Neutrophilic Leukemia | Toxic Epidermal Necrolysis | Primary Pigmented Nodular Adrenocortical Disease | Heterotaxy | Optic Neuropathy, Anterior Ischemic | Glutaric Aciduria Type 1 | Relapsing Polychondritis | Hyperammonemia | Non-Hodgkin Lymphoma | Obsessive-compulsive Disorder | Hyperthyroidism | B-cell Prolymphocytic Leukemia | Primary Progressive Nonfluent Aphasia | Postaxial Polydactyly | Hemolytic Uremic Syndrome, Atypical | Juvenile Myelomonocytic Leukemia | Auriculocondylar Syndrome | Reticular Dysgenesis | Spinocerebellar Ataxia Type 1 | Anorectal Fistula | Metabolic Diseases | Waardenburg Syndrome | Left Ventricular Noncompaction | Epilepsy Of Infancy With Migrating Focal Seizures | Sarcoma, Ewing | Thanatophoric Dysplasia Type 1 | Hepatic Adenomatosis | Vici Syndrome | Congenital Absence Of Vas Deferens | Muscular Dystrophy | Mumps | Diabetic Encephalopathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Dengue Shock Syndrome | Specific Granule Deficiency | Antenatal Bartter Syndrome Type 1 | Mucolipidosis Type III | Chronic Leukemia | Pulmonary Veno-occlusive Disease | Mevalonate Kinase Deficiency | Methemoglobinemia | Crouzon Syndrome With Acanthosis Nigricans | Lafora Disease | Thyroid Hormone Resistance | Batten Disease | Long QT Syndrome Type 2 | Yellow Fever | Maple Syrup Urine Disease | Creutzfeldt-Jakob Disease | GM2-gangliosidosis AB Variant | Optic Atrophy 2 | Myofibromatosis | Hereditary Multiple Exostoses | Renal Medullary Carcinoma | Charcot-Marie-Tooth Disease, Type 2 | Persistent Hyperplastic Primary Vitreous | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Joubert Syndrome | Common Variable Immunodeficiency | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Melanoma, Uveal | Nemaline Myopathy | Hoyeraal-Hreidarsson Syndrome | Spondyloarthritis | Asthma, Nocturnal | Lattice Corneal Dystrophy | Sclerosteosis | Pulmonary Sclerosing Hemangioma | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Macular Degeneration | Malaria, Cerebral | Schizotypal Personality Disorder | Cryptococcal Meningitis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Acute Motor Axonal Neuropathy | Colitis, Collagenous | Chronic Myeloid Leukemia | Pulmonary Tuberculosis | Paroxysmal Kinesigenic Dyskinesia | Chudley-McCullough Syndrome