Miyoshi Myopathy

About the Disease
Miyoshi Muscular Dystrophy 1, also known as miyoshi myopathy, is related to muscular dystrophy, becker type and muscular dystrophy, limb-girdle, autosomal recessive 1, and has symptoms including decreased grip strength An important gene associated with Miyoshi Muscular Dystrophy 1 is DYSF (Dysferlin), and among its related pathways/superpathways are miRNAs involvement in the immune response in sepsis and miRNAs involved in DNA damage response. The drugs Deflazacort and Immunosuppressive Agents have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, heart and brain, and related phenotypes are pelvic girdle muscle weakness and difficulty walking

Common Targets
DYSF | ANO5 | SMPD1

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

Other Diseases

Ataxia-ocular Apraxia 2 | Charcot-Marie-Tooth Disease | Spinocerebellar Ataxia Type 20 | Riboflavin Transporter Deficiency Neuronopathy | Epidermolysis Bullosa Simplex | Oral Lichen Planus | Peyronie's Disease | Schwartz-Jampel-Aberfeld Syndrome | Cold Agglutinin Disease | Epidermolysis Bullosa | Macrophage Activation Syndrome | Pouchitis | Hypersomnia | Leishmaniasis, Visceral | Wolcott-Rallison Syndrome | Spinocerebellar Ataxia Type 42 | Congenital Muscular Dystrophy | Mucolipidosis Type III | Hypoproteinemia, Hypercatabolic | Intracerebral Hemorrhage | Fibromyalgia | Cutis Laxa | Onchocerciasis | Acrodermatitis Enteropathica | Raynaud Phenomenon | Dyggve-Melchior-Clausen Disease | Woodhouse-Sakati Syndrome | Persistent Truncus Arteriosus | Glanzmann Thrombasthenia | Pernicious Anemia | Glycogen Storage Disease Type 1b | Gout | B-cell Prolymphocytic Leukemia | Budd-Chiari Syndrome | Methemoglobinemia Type IV | Thin Basement Membrane Disease | Essential Fructosuria | Rubinstein-Taybi Syndrome | Primrose Syndrome | Myeloid Leukemia | ICF Syndrome | Esophagitis | Premenstrual Syndrome | Familial Male-limited Precocious Puberty | Schizoaffective Disorder | Neuroblastoma | Hennekam Lymphangiectasia-lymphedema Syndrome | Dysferlinopathy | Heterotopic Ossification | Chronic Periodontitis | Uremic Pruritus | Granular Corneal Dystrophy | Ocular Albinism Type 1 | Syndactyly | Viral Meningitis | Metanephric Adenoma | Bloom Syndrome | Tremor | Seizures-scoliosis-macrocephaly Syndrome | Antley-Bixler Syndrome | Hypopigmentation | Pemphigus | Acute Motor Axonal Neuropathy | Atelosteogenesis Type 2 | Pulmonary Stenosis | Batten Disease | Hepatic Adenomatosis | Primary Erythromelalgia | Sleep Disorder | Yellow Fever | Glutathione Synthetase Deficiency | Cryptorchidism | Intestinal Hypomagnesemia 1 | Congenital Central Hypoventilation Syndrome | Nager Acrofacial Dysostosis | Tonsillitis | Carcinoma, Signet Ring Cell | Micro Syndrome | Spinocerebellar Ataxia Type 23 | Hereditary Neuropathy With Liability To Pressure Palsies | Arthritis | Strabismus | Photosensitivity | Chediak-Higashi Syndrome | Cerebrovascular Disorders | Imerslund-Grasbeck Syndrome | Motion Sickness | Schizophrenia, Paranoid | Multiple System Atrophy | Behcet's Disease | Patent Ductus Arteriosus | Conjunctivitis, Allergic | McCune-Albright Syndrome | Hemochromatosis | Dystonia Musculorum Deformans | Cocaine-Related Disorders | Lupus Erythematosus | Urolithiasis | Polycythemia | Neurofibromatosis | Precocious Puberty | GLUT1 Deficiency Syndrome | Hypertrophy | Hemorrhoids | Fowler's Syndrome | Best Macular Dystrophy | X-linked Charcot-Marie-Tooth Disease | Adrenomyeloneuropathy | Sporadic Hemiplegic Migraine | Lymphoproliferative Disorders | Chondrosarcoma | Carbohydrate Metabolism Disorders | Thrombocythemia, Essential | Lymphopenia | Cystitis | Ocular Surface Squamous Neoplasia | Scapuloperoneal Spinal Muscular Atrophy | Urethritis | Hemangioendothelioma | Nemaline Myopathy 10 | Trismus-pseudocamptodactyly Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Fetal Alcohol Syndrome | Galloway-Mowat Syndrome | Wieacker-Wolff Syndrome | 3-methylglutaconic Aciduria Type I | Hypertensive Nephropathy | Glycogen Storage Disease Type 6 | Pre-eclampsia | Dermatitis Herpetiformis | Robinow Syndrome | Skin Fragility-woolly Hair Syndrome | Systemic Lupus Erythematosus | Hepatitis, Alcoholic | Thalassemia | Tay-Sachs Disease | Dental Caries | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Hyperparathyroidism, Secondary | Sarcoma, Endometrial Stromal | Histiocytosis | Focal Segmental Glomerulosclerosis | Mitochondrial Cytopathy | Retinal Dystrophy, Early-onset Severe | Autoimmune Polyendocrine Syndrome | Muscle Wasting | Neurogenic Bladder | Atopic Dermatitis | Pituitary Disorders | Optic Neuropathy | Hyperbilirubinemia, Neonatal | Cerebral Cavernous Malformations | Pulmonary Veno-occlusive Disease | Acne Vulgaris | Stuttering | Proximal Symphalangism | Treacher Collins Syndrome | Lymphoma | Coloboma | Blastomycosis | Porphyria, Acute Intermittent | Meningeal Melanocytoma | Oculocutaneous Albinism Type 4 | Down Syndrome | Microphthalmia | Takayasu's Arteritis | Biotinidase Deficiency | Cramp Fasciculation Syndrome | Thrombophlebitis | COACH Syndrome | Bone Marrow Necrosis | Moyamoya Disease | Intracranial Hypertension | Cyst | Osteosclerosis | Acanthosis Nigricans | Hernia, Inguinal | Familial Hypobetalipoproteinemia | Retinitis Pigmentosa 3 | Congenital Lipoid Adrenal Hyperplasia | Juvenile Myelomonocytic Leukemia | Carotid Artery Disease | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Lipoma | Cholera | Prurigo Nodularis | Anorchia | Liver Diseases | Progressive External Ophthalmoplegia | Keratopathy | Angiosarcoma Of The Breast | Menkes Disease | Multiple Sulfatase Deficiency | Neutrophilia | Anodontia | Jacobsen Syndrome | Craniofrontonasal Syndrome | Mood Disorder | Prediabetes | Trichothiodystrophy | Fibrodysplasia Ossificans Progressiva | Antithrombin III Deficiency | Rotor Syndrome | Glycogen Storage Disease Type 0 | Charcot-Marie-Tooth Disease, Type 1A | Early Infantile Epileptic Encephalopathy 13 | Hyperparathyroidism | Trichuriasis | Adenosine Deaminase Deficiency | Olmsted Syndrome | Nail Disorder, Nonsyndromic Congenital | Otosclerosis | Spinocerebellar Ataxia Type 21 | Potocki-Shaffer Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Milk Allergy | Autosomal Recessive Bestrophinopathy | HIBCH Deficiency | Lymphoma, Mantle Cell | Blepharo-cheilo-odontic Syndrome | Marinesco-Sjogren Syndrome | Auriculocondylar Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Meningococcal Meningitis | Dermatitis | Ghosal Syndrome | Pemphigus Foliaceus | Ehlers-Danlos Syndrome | Carcinoma, Small Cell | Fetal Akinesia Deformation Sequence | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Macrophagic Myofasciitis | Hypotension, Orthostatic | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Patent Foramen Ovale | Diabetes Insipidus | Pemphigus Vulgaris | Primary Sclerosing Cholangitis | Choroideremia | Hemangioma | Tetraplegia | Myocardial Infarction | Alopecia Totalis | Supravalvular Aortic Stenosis | Rickets | Osteogenesis Imperfecta Type V | Nemaline Myopathy | Muscular Dystrophy | Cornelia De Lange Syndrome | Warsaw Breakage Syndrome | Spastic Paraplegia Type 7 | Cancer, Brain | Harlequin Ichthyosis | Spitzoid Melanoma | Steel Syndrome | Glaucomatocyclitic Crisis | Megalencephaly | Epidermal Nevus Syndrome | Purpura, Thrombotic Thrombocytopenic | Tetanus | Acute Myeloid Leukemia | Schizotypal Personality Disorder | Neurocutaneous Syndromes | Adult Polyglucosan Body Disease | Stevens-Johnson Syndrome | Androgen Insensitivity | Hepatitis A | Histiocytic Sarcoma | Liddle Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Distal Spinal Muscular Atrophy | Hypoparathyroidism | Clouston Hidrotic Ectodermal Dysplasia | Nasodigitoacoustic Syndrome | Dengue Shock Syndrome | Metatropic Dysplasia | Presbycusis | Irritable Bowel Syndrome | Conn Syndrome | Primary Aldosteronism | Eosinophilia | Fetal And Neonatal Alloimmune Thrombocytopenia | Fucosidosis | Poikiloderma With Neutropenia | Pancytopenia | Kidney Stones | Cohen Syndrome | Pulmonary Alveolar Proteinosis | Congenital Hereditary Endothelial Dystrophy Type II | Persistent Fetal Circulation | REM Sleep Behavior Disorder | Nephronophthisis | C3 Glomerulopathy | Lymphoma, AIDS-related | Vertigo | Heroin Dependence | Long QT Syndrome Type 2 | Swine Influenza | Spinal Muscular Atrophy | Brachial Plexus Neuropathy | Herpes Simplex Dermatitis | Osteoglophonic Dysplasia | Varicocele | Pontocerebellar Hypoplasia Type 7 | Angioimmunoblastic T-cell Lymphoma | Scleroderma, Diffuse | Infantile Liver Failure Syndrome 1 | Iron Metabolism Disorders | Eccrine Porocarcinoma | Williams Syndrome | Diastrophic Dysplasia | Senior-Loken Syndrome | Ulcerative Colitis | Paroxysmal Nocturnal Hemoglobinuria | Gastric Atrophy | Blepharophimosis Syndrome | Nicotine Addiction | Marfan Syndrome | Neuroectodermal Tumors, Primitive | Ovarian Hyperstimulation Syndrome | Esotropia | AIDS | Malnutrition | Diabetes Insipidus, Nephrogenic | Esophageal Adenocarcinoma | Basal Cell Nevus Syndrome | Oculopharyngeal Muscular Dystrophy | Charcot-Marie-Tooth Disease, Type 6 | Facioscapulohumeral Muscular Dystrophy Type 1 | Nance-Horan Syndrome | Reticular Dysgenesis | Asperger Syndrome | Cholestasis, Intrahepatic | Metachromatic Leukodystrophy | Muir-Torre Syndrome | Gliosarcoma | DRESS Syndrome | Alagille Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Vaginitis | Cushing Syndrome | Blepharoconjunctivitis | Hemochromatosis Type 1 | Arthropathy | Urofacial Syndrome | Achromatopsia | Liver Failure, Acute Infantile | Meningioma | Spinocerebellar Ataxia Type 12 | Lichen Sclerosus | Optic Neuritis | Hypogonadism | Hereditary Mixed Polyposis Syndrome | Cholangiocarcinoma | Peroxisomal Disorder | Pierson Syndrome | Klinefelter Syndrome | Contact Dermatitis | Rhizomelic Chondrodysplasia Punctata | Pierpont Syndrome | Branchiootorenal Syndrome | Botulism | Behavioral Variant Of Frontotemporal Dementia | Hypertension, Essential | Extramammary Paget's Disease | Progressive Familial Intrahepatic Cholestasis | Gynecomastia | Follicular Dendritic Cell Sarcoma | Urea Cycle Disorder | Shprintzen-Goldberg Syndrome | VACTERL/VATER Association | Dermatofibrosarcoma | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Myotonic Disorders | Pseudo-pseudohypoparathyroidism | Myelomeningocele | Kabuki Syndrome | Glioblastoma Multiforme | Twin-to-twin Transfusion Syndrome | Tendinopathy | Aldosteronism | Hemimegalencephaly | Majeed Syndrome | POEMS Syndrome | Intermittent Explosive Disorder | Osteitis | Diabetic Macular Edema | Hydronephrosis | Esophagitis, Eosinophilic | Chromosome 8q21.11 Deletion Syndrome | Hypotrichosis Simplex | Congenital Disorders Of Glycosylation Type II | Gnathodiaphyseal Dysplasia | Carpal Tunnel Syndrome | Inflammatory Joint Disease | Colitis, Microscopic | Mast Cell Leukemia | Congenital Nephrotic Syndrome | Cheilitis | T-cell Prolymphocytic Leukemia