Distal Myopathy

About the Disease
Miyoshi Muscular Dystrophy, also known as distal myopathy, is related to myopathy, distal, 1 and miyoshi muscular dystrophy 3. An important gene associated with Miyoshi Muscular Dystrophy is MPD3 (Myopathy, Distal 3), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. The drugs Deflazacort and Glucosamine have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, heart and bone, and related phenotypes are Decreased viability and Decreased viability

Common Targets
GNE | FLNC | OBSCN | TIA1 | ADSS1 | MATR3 | DNAJB6 | TTN | TCAP | ACTA1 | MYH7 | G8878 | DES | NEB

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Chromosome 8q21.11 Deletion Syndrome | Distal Spinal Muscular Atrophy | Idiopathic Pulmonary Fibrosis | Congenital Nystagmus | Pituitary Disorders | Angina Pectoris | Burn-McKeown Syndrome | C3 Glomerulonephritis | Hereditary Neuropathy With Liability To Pressure Palsies | Cardiospondylocarpofacial Syndrome | Myocardial Infarction | Phenylketonuria | Methemoglobinemia | Proctitis | Lymphoma, Follicular | Optic Neuropathy | Lissencephaly 2 | Klippel-Feil Syndrome | Ependymoma | Cavitary Optic Disc Anomalies | Otosclerosis | Irritable Bowel Syndrome | Hepatopulmonary Syndrome | Myocarditis | Arterial Tortuosity Syndrome | Cancer, Colon | Spinocerebellar Ataxia Type 42 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Discoid Lupus Erythematosus | Cluster Headache | Microphthalmia | Inflammatory Bowel Disease | Emery-Dreifuss Muscular Dystrophy | Saul-Wilson Syndrome | Adenylosuccinate Lyase Deficiency | Keratocystic Odontogenic Tumor | Diarrhea | 3-hydroxy-3-methylglutaric 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Spreading Melanoma | Phenylketonuria II | Analgesia | Abetalipoproteinemia | Muir-Torre Syndrome | Congenital Nephrotic Syndrome | Granular Corneal Dystrophy | Angiomyolipoma | Syphilis | Chromosome 5q Deletion Syndrome | Bicuspid Aortic Valve | Pneumonia, Viral | Erythrokeratodermia Variabilis | Fetal And Neonatal Alloimmune Thrombocytopenia | Cholangitis | Fibromyalgia | Reye Syndrome | GATA2 Deficiency | Tendinopathy | Lymphoma, B-cell | Insulinoma | Distal Myopathy 2 | Kernicterus | Patent Foramen Ovale | Sponastrime Dysplasia | Avian Influenza | Nephrotic Syndrome | Tyrosinemia Type 1 | Anorectal Malformations | Paroxysmal Nocturnal Hemoglobinuria | Hydrocephalus | Weill-Marchesani Syndrome | Toxic Epidermal Necrolysis | Schistosomiasis | Anuria | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Ameloblastic Carcinoma | Fabry's Disease | Lennox-Gastaut Syndrome | Amelogenesis Imperfecta | Amish Infantile Epilepsy Syndrome | Lattice Corneal Dystrophy Type 1 | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Hypodontia | Odonto-onycho-dermal Dysplasia | Smoldering Myeloma | Chondroma | VEXAS Syndrome | Cervical Dystonia | Hypoalbuminemia | Primary Familial Brain Calcification | Retinoblastoma | Hemorrhagic Disorders | Spermatocele | Ophthalmia, Sympathetic | Kashin-Beck Disease | Leigh Syndrome | Hereditary Pyropoikilocytosis | Japanese Encephalitis | Alexander Disease | Clouston Hidrotic Ectodermal Dysplasia | Thrombotic Microangiopathy | Carotid Artery Disease | Pleomorphic Xanthoastrocytoma | Chronic Granulomatous Disease | Pyoderma Gangrenosum | Facioscapulohumeral Muscular Dystrophy | Exfoliative Dermatitis | Hereditary Inclusion Body Myopathy | Hypospadias | Vitamin K Deficiency | Choroideremia | Pregnancy, Ectopic | Infantile Liver Failure Syndrome 1 | ICF Syndrome | Behcet's Disease | Oligodendroglioma | Polycythemia | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Early 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