Charcot-Marie-Tooth Disease (CMT)

Also known as Hereditary Motor and Sensory Neuropathy, Dejerine-Sottas Disease, and Peroneal Muscular Atrophy.

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Cure CMT4J: Advancing Gene Therapy for Rare Diseases 100/5 1 2 3 4 5 Cure CMT4J is generating awareness and support for the development of gene therapy to address CMT4J Details Rate Report

CMT Foundation 0/5 1 2 3 4 5 The Charcot-Marie-Tooth CMT Foundation is dedicated to raising awareness and funds for Charcot-Marie Details Rate Report

The Foundation For Peripheral Neuropathy® 0/5 1 2 3 4 5 The Foundation for Peripheral Neuropathy strives to cure painful neuropathies through collaborativ Details Rate Report

Hereditary Neuropathy Foundation 0/5 1 2 3 4 5 HNF is the leading patient advocacy organization for those affected by hereditary neuropathy includi Details Rate Report

Charcot-Marie-Tooth Association | Fighting to end CMT 0/5 1 2 3 4 5 CMTA Headlines: Details Rate Report

Search for in All Categories International- Canada Neuromuscular Diseases Acid Maltase Deficiency (AMD) Amyotrophic Lateral Sclerosis (ALS) Andersen-Tawil Syndrome Becker Muscular Dystrophy (BMD) Becker Myotonia Congenita Bethlem Myopathy Carnitine Deficiency Carnitine Palmityl Transferase Deficiency (CPT Deficiency) Central Core Disease (CCD) Centronuclear Myopathy Charcot-Marie-Tooth Disease (CMT) Congenital Muscular Dystrophy (CMD) Congenital Myasthenic Syndromes (CMS) Congenital Myotonic Dystrophy Debrancher Enzyme Deficiency Dermatomyositis (DM) Distal Muscular Dystrophy (DD) Duchenne Muscular Dystrophy (DMD) Emery-Dreifuss Muscular Dystrophy (EDMD) Endocrine Myopathies Facioscapulohumeral Muscular Dystrophy (FSH or FSHD) Finnish (Tibial) Distal Myopathy Friedreich’s Ataxia (FA) Fukuyama Congenital Muscular Dystrophy Glycogenosis Gowers-Laing Distal Myopathy Hereditary Inclusion-Body Myositis Hyperthyroid Myopathy Hypothyroid Myopathy Inclusion-Body Myositis (IBM) Inherited Myopathies Integrin-Deficient Congenital Muscular Dystrophy Lactate Dehydrogenase Deficiency Lambert-Eaton Myasthenic Syndrome (LEMS) Limb-Girdle Muscular Dystrophy (LGMD) Merosin-Deficient Congenital Muscular Dystrophy Mitochondrial Myopathy Miyoshi Distal Myopathy Motor Neurone Disease Muscle-Eye-Brain Disease Myasthenia Gravis (MG) Myoadenylate Deaminase Deficiency Myofibrillar Myopathy Myophosphorylase Deficiency Myotonia Congenita (MC) Myotonic Muscular Dystrophy (MMD) Myotubular Myopathy (MTM or MM) Nemaline Myopathy Nonaka Distal Myopathy Oculopharyngeal Muscular Dystrophy (OPMD) Paramyotonia Congenita Pearson Syndrome Periodic Paralysis Phosphofructokinase Deficiency Phosphoglycerate Kinase Deficiency Phosphoglycerate Mutase Deficiency Phosphorylase Deficiency Polymyositis (PM) Progressive External Ophthalmoplegia (PEO) Spinal Muscular Atrophy (SMA) Spinal-Bulbar Muscular Atrophy (SBMA) Ullrich Congenital Muscular Dystrophy Welander Distal Myopathy ZASP-Related Myopathy United States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Search