Informaţii despre

Nume Muscular Atrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli musculare; Boli neuronale; Boli osoase
Boli din aceeaşi familie Progressive Muscular Atrophy

Vezi şi

Boli A-Z Abdominal Wall Defect Acute Respiratory Distress Syndrome Adrenoleukodystrophy Aging Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Beta2m Amyotonia Congenita Amyotrophy, Monomelic Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Anterior Spinal Artery Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autonomic Dysfunction Axonal Neuropathy Beckwith-Wiedemann Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Wright Antigen Bone Fracture Candidiasis Cataract Central Core Myopathy Cerebellar Hypoplasia Cerebritis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2d Charcot-Marie-Tooth Disease, Axonal, Type 2e Charcot-Marie-Tooth Disease, Axonal, Type 2k Charcot-Marie-Tooth Disease Type 2c Charge Syndrome Chiari Malformation Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosomal Triplication Clubfoot Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Congenital Hypothyroidism Corneal Dystrophy, Thiel-Behnke Type Cortical Dysplasia, Complex, with Other Brain Malformations 7 Cystic Fibrosis Cystinuria Dandy-Walker Complex Dentatorubral-Pallidoluysian Atrophy Diabetes Mellitus Distal Hereditary Motor Neuropathies Distal Hereditary Motor Neuropathy Type 7 Distal Hereditary Motor Neuropathy, Type V Dracunculiasis Dysautonomia Dysphagia Ehlers-Danlos Syndrome Encephalitis Encephalopathy Epilepsy Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Essential Tremor Exophthalmic Ophthalmoplegia Exudative Vitreoretinopathy Farber Lipogranulomatosis Flna-Related Periventricular Nodular Heterotopia Fragile X Syndrome Galactose Epimerase Deficiency Gynecomastia Hepatic Adenomas, Familial Hereditary Ataxia Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hip Subluxation Hypersomnia Hypertonia Hypoplastic Left Heart Syndrome Hypotonia Hypoxia Inclusion Body Myositis Infant Gynecomastia Intestinal Pseudo-Obstruction Joint Disorders Juvenile Spinal Muscular Atrophy Kagami-Ogata Syndrome Kaposiform Hemangioendothelioma Kaufman Oculocerebrofacial Syndrome Laryngitis Lateral Sclerosis Limb-Girdle Muscular Dystrophy Lipodystrophy Long Qt Syndrome 1 Machado-Joseph Disease Majeed Syndrome Mcleod Syndrome Microcytic Anemia Microphthalmia, Isolated 1 Motor Neuron Disease Mucolipidosis Iv Multifocal Motor Neuropathy Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Muscle Hypertrophy Muscular Dystrophy Muscular Dystrophy, Duchenne and Becker Type Myasthenia Gravis Myoclonus Myopathy Myositis Myotonia Myotonic Dystrophy Neonatal Adrenoleukodystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronitis Neuronopathy, Distal Hereditary Motor, Type Va Neuronopathy, Distal Hereditary Motor, Type Viia Neuropathy Occipital Horn Syndrome Oculopharyngeal Muscular Dystrophy Olivopontocerebellar Atrophy Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Pancreatitis Panniculitis Paraplegia Pelizaeus-Merzbacher Disease Plexiform Neurofibroma Poland Syndrome Poliomyelitis Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 1a Pontocerebellar Hypoplasia, Type 1c Porphyria Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures Progressive Muscular Atrophy Prostate Cancer Prostatitis Proximal Spinal Muscular Atrophy Retinitis Rett Syndrome Rhabdomyosarcoma Rothmund-Thomson Syndrome Roussy-Levy Hereditary Areflexic Dystasia Sapho Syndrome Scapuloperoneal Spinal Muscular Atrophy Scoliosis Sleep Disorder Spasticity Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Disease Spinal Muscular Atrophy Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy Spinal Muscular Atrophy, X-Linked 2 Status Epilepticus Survival Motor Neuron Spinal Muscular Atrophy Tetanus Thrombosis Tooth Disease Tremor Wallerian Degeneration