Informaţii despre

Nume Motor Neuron Disease
Pagina Web www.malacards.org
Clasificari ICD10 Motor neuron disease
Clasificare anatomică Malacards Boli neuronale

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Boli A-Z Adenoma Aging Al Amyloidosis Albinism Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloid Neuropathy Amyloidosis Amyotrophic Lateral Sclerosis 1 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia Amyotrophic Lateral Sclerosis 11 Amyotrophic Lateral Sclerosis 16, Juvenile Amyotrophic Lateral Sclerosis 18 Amyotrophic Lateral Sclerosis 19 Amyotrophic Lateral Sclerosis 21 Amyotrophic Lateral Sclerosis 2, Juvenile Amyotrophic Lateral Sclerosis 4, Juvenile Amyotrophic Lateral Sclerosis 7 Amyotrophic Lateral Sclerosis 9 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 6 Amyotrophy, Monomelic Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Aphasia Apraxia Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Associative Agnosia Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Axonal Neuropathy Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Breast Cancer Breast Fibrosarcoma Brown-Vialetto-Van Laere Syndrome Bullous Pemphigoid Camptocormism Cerebral Atrophy Cerebritis Cervicitis Charcot-Marie-Tooth Disease Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Progressive External Ophthalmoplegia Cone-Rod Dystrophy 2 Creutzfeldt-Jakob Disease Cytoplasmic Body Myopathy Dementia Diabetic Neuropathy Distal Hereditary Motor Neuropathies Dysphagia Encephalopathy Epilepsy Expressive Language Disorder Fazio-Londe Disease Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gout Granulomatous Myositis Hereditary Spastic Paraplegia Hyperparathyroidism Hypertrophic Cardiomyopathy Hypochondroplasia Hypomelanosis of Ito Hypoxia Ideomotor Apraxia Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Inclusion Body Myositis Insulin-Like Growth Factor I Juvenile Amyotrophic Lateral Sclerosis Juvenile Spinal Muscular Atrophy Krabbe Disease Laryngitis Lateral Sclerosis Lathyrism Lethal Congenital Contracture Syndrome 1 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lewis-Sumner Syndrome Locked-in Syndrome Lymphoma Machado-Joseph Disease Madras Motor Neuron Disease Malignant Hyperthermia Malignant Hyperthermia Susceptibility Marchiafava Bignami Disease Miller Fisher Syndrome Monoclonal Paraproteinemia Mucolipidosis Iv Multifocal Motor Neuropathy Multiple Sclerosis Muscular Atrophy Myasthenia Gravis Myopathy Myositis Neurodegeneration with Brain Iron Accumulation 2a Neurogenic Bladder Neuronal Migration Disorders Neuronitis Neuronopathy, Distal Hereditary Motor, Type Viib Neuropathy Neutrophilic Dermatosis, Acute Febrile Nominal Aphasia Oculocutaneous Albinism Olivopontocerebellar Atrophy Paget's Disease of Bone Papillon-Lefevre Syndrome Paraplegia Parathyroid Adenoma Perry Syndrome Phonagnosia Pick Disease of Brain Pleomorphic Liposarcoma Poliomyelitis Polymyositis Polyneuropathy Pontocerebellar Hypoplasia Postpoliomyelitis Syndrome Potocki-Lupski Syndrome Primary Cerebellar Degeneration Primary Hyperparathyroidism Primary Lateral Sclerosis, Adult, 1 Progressive Bulbar Palsy Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Muscular Atrophy Progressive Non-Fluent Aphasia Proximal Spinal Muscular Atrophy Pseudobulbar Palsy Pure Autonomic Failure Raine Syndrome Renal Glucosuria Renal Nutcracker Syndrome Riboflavin Transporter Deficiency Neuronopathy Sandhoff Disease Schizophrenia Seizures, Benign Familial Neonatal, 1 Semantic Dementia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Spasticity Speech and Communication Disorders Spinal Disease Spinal Muscular Atrophy Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Spinocerebellar Ataxia 11 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 36 Spinocerebellar Degeneration Spondylosis Status Epilepticus Stiff-Person Syndrome Striatonigral Degeneration Superficial Siderosis Supranuclear Palsy, Progressive, 1 Survival Motor Neuron Spinal Muscular Atrophy Sveinsson Chorioretinal Atrophy Tay-Sachs Disease Temporal Lobe Epilepsy Thyroiditis Tic Disorder Tooth Disease Traumatic Brain Injury Wernicke Encephalopathy