Informaţii despre

Nume Amyotrophic Lateral Sclerosis 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Motor neuron disease
Clasificare anatomică Malacards Boli neuronale; Boli psihice
Boli din aceeaşi familie Amyotrophic Lateral Sclerosis 11; Amyotrophic Lateral Sclerosis 12; Amyotrophic Lateral Sclerosis 16, Juvenile; Amyotrophic Lateral Sclerosis 17; Amyotrophic Lateral Sclerosis 18; Amyotrophic Lateral Sclerosis 19; Amyotrophic Lateral Sclerosis 2, Juvenile; Amyotrophic Lateral Sclerosis 20; Amyotrophic Lateral Sclerosis 21; Amyotrophic Lateral Sclerosis 23; Amyotrophic Lateral Sclerosis 3; Amyotrophic Lateral Sclerosis 4, Juvenile; Amyotrophic Lateral Sclerosis 5, Juvenile; Amyotrophic Lateral Sclerosis 7; Amyotrophic Lateral Sclerosis 8; Amyotrophic Lateral Sclerosis 9; Amyotrophic Lateral Sclerosis Type 14; Amyotrophic Lateral Sclerosis Type 15; Amyotrophic Lateral Sclerosis Type 22; Amyotrophic Lateral Sclerosis Type 5; Amyotrophic Lateral Sclerosis Type 6

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Boli A-Z Ablepharon-Macrostomia Syndrome Acromegaly Adenoma Adie Pupil Aging Agraphia Alexander Disease Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amnestic Disorder Amyloidosis Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia Amyotrophic Lateral Sclerosis 11 Amyotrophic Lateral Sclerosis 12 Amyotrophic Lateral Sclerosis 16, Juvenile Amyotrophic Lateral Sclerosis 17 Amyotrophic Lateral Sclerosis 18 Amyotrophic Lateral Sclerosis 19 Amyotrophic Lateral Sclerosis 20 Amyotrophic Lateral Sclerosis 21 Amyotrophic Lateral Sclerosis 23 Amyotrophic Lateral Sclerosis 2, Juvenile Amyotrophic Lateral Sclerosis 3 Amyotrophic Lateral Sclerosis 4, Juvenile Amyotrophic Lateral Sclerosis 5, Juvenile Amyotrophic Lateral Sclerosis 7 Amyotrophic Lateral Sclerosis 8 Amyotrophic Lateral Sclerosis 9 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 15 Amyotrophic Lateral Sclerosis Type 22 Amyotrophic Lateral Sclerosis Type 5 Amyotrophic Lateral Sclerosis Type 6 Amyotrophy, Monomelic Anaplastic Ganglioglioma Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anosognosia Anterior Horn Cell Disease Aphasia Apraxia Arterial Tortuosity Syndrome Arthrochalasia Ehlers-Danlos Syndrome Askin's Tumor Associative Agnosia Astroblastoma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Attention Deficit-Hyperactivity Disorder Autoimmune Disease Autonomic Dysfunction Autonomic Nervous System Neoplasm Axenfeld-Rieger Syndrome Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Binswanger's Disease Black Hairy Tongue Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Borna Disease Brain Cancer Brain Injury Brain Ischemia Breast Cancer Breast Fibrosarcoma Brown-Vialetto-Van Laere Syndrome Bullous Pemphigoid C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Cannabis Abuse Cardiac Arrest Central Nervous System Disease Central Nervous System Teratoma Central Neurocytoma Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Atrophy Cerebral Degeneration Cerebral Hemorrhage Cerebritis Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2cc Charcot-Marie-Tooth Disease Type 2a Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 Chiari Malformation Cholecystitis Cholelithiasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Cone-Rod Dystrophy 2 Corticobasal Degeneration Crouzon Syndrome with Acanthosis Nigricans Dementia Dementia, Lewy Body Demyelinating Polyneuropathy Diabetic Neuropathy Dicarboxylic Aminoaciduria Distal Hereditary Motor Neuropathies Down Syndrome Dyschromatosis Symmetrica Hereditaria Dysembryoplastic Neuroepithelial Tumor Dysphagia Dystonia Early-Onset, Autosomal Dominant Alzheimer Disease Encephalopathy Endotheliitis Eosinophilic Fasciitis Ependymoblastoma Epilepsy Episodic Ataxia, Type 6 Epithelial Recurrent Erosion Dystrophy Essential Tremor Expressive Language Disorder Extraosseous Chondrosarcoma Fabry Disease Facial Onset Sensory and Motor Neuronopathy Fanconi Anemia, Complementation Group E Fasciitis Foramen Magnum Meningioma Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gangliocytoma Ganglioglioma Ganglioneuroma Genitopatellar Syndrome Gynecomastia Hairy Tongue Head Injury Hepatic Adenomas, Familial Hepatic Encephalopathy Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Spastic Paraplegia Huntington Disease Hyperparathyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoganglionosis Hypoparathyroidism Hypoxia Ideomotor Apraxia Inclusion Body Myositis Infant Gynecomastia Insulin-Like Growth Factor I Intermittent Claudication Ischemia Juvenile Amyotrophic Lateral Sclerosis Juvenile Spinal Muscular Atrophy Kartagener Syndrome Klippel-Feil Syndrome Lateral Sclerosis Lathyrism Legius Syndrome Lethal Congenital Contracture Syndrome 1 Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Liposarcoma Low Tension Glaucoma Lyme Disease Machado-Joseph Disease Macroglobulinemia Macroglossia Malignant Spiradenoma Meckel Syndrome, Type 1 Medulloepithelioma Menkes Disease Miller-Dieker Lissencephaly Syndrome Mills Syndrome Mitochondrial Complex I Deficiency Mitochondrial Disorders Motor Neuron Disease Multifocal Motor Neuropathy Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple System Atrophy 1 Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Myasthenia Gravis Myeloma, Multiple Myoclonus Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myositis Myotonic Dystrophy Myxoid Chondrosarcoma Nemaline Myopathy Neonatal Hypoxic and Ischemic Brain Injury Nervous System Disease Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation Neuroendocrine Tumor Neurofibroma Neuromuscular Disease Neuromyelitis Optica Neuronal Ceroid-Lipofuscinoses Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type V Neurosarcoidosis Neurosyphilis Neutrophil Actin Dysfunction Nominal Aphasia Non-Involuting Congenital Hemangioma Obsessive-Compulsive Disorder Ocular Dominance Oculopharyngeal Muscular Dystrophy Olfactory Neuroblastoma Olivopontocerebellar Atrophy Opitz Gbbb Syndrome, Type Ii Optic Nerve Glioma Papilloma Paralytic Poliomyelitis Paraplegia Pathological Gambling Patulous Eustachian Tube Pepsinogen 3, Group I Periodontitis, Aggressive, 1 Peripheral Nervous System Neoplasm Perry Syndrome Phonagnosia Pick Disease of Brain Pituitary Adenoma Poems Syndrome Poliomyelitis Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polykaryocytosis Inducer Polymicrogyria Polyneuropathy Polyradiculoneuropathy Polyradiculopathy Pompholyx Postencephalitic Parkinson Disease Postpoliomyelitis Syndrome Primary Progressive Multiple Sclerosis Prion Disease Progressive Muscular Atrophy Progressive Non-Fluent Aphasia Prosopagnosia Prostatitis Proximal Spinal Muscular Atrophy Pseudobulbar Palsy Pulmonary Alveolar Microlithiasis Reflex Sympathetic Dystrophy Renal Glucosuria Respiratory Failure Restless Legs Syndrome Retinitis Rubinstein-Taybi Syndrome 1 Sarcoma Satb2-Associated Syndrome Schistosomiasis Schizophrenia Scrapie Seizures, Benign Familial Neonatal, 1 Semantic Dementia Siderosis Sleep Apnea Spasmodic Dysphonia Spasticity Spastic Paraparesis Spastic Paraplegia 11 Spastic Paraplegia 35, Autosomal Recessive Spastic Paraplegia 4, Autosomal Dominant Spastic Paraplegia 57, Autosomal Recessive Speech and Communication Disorders Speech Disorder Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 36 Split Hand Spondylosis Status Epilepticus Superficial Siderosis Superficial Siderosis of the Central Nervous System Supranuclear Palsy, Progressive, 1 Survival Motor Neuron Spinal Muscular Atrophy Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Synucleinopathy Tardbp-Related Amyotrophic Lateral Sclerosis Temporal Lobe Epilepsy Tendinosis Tooth Disease Toxic Encephalopathy Transient Cerebral Ischemia Transient Global Amnesia Tremor Tropical Spastic Paraparesis Ulnar Nerve Lesion Variably Protease-Sensitive Prionopathy Vascular Dementia Von Economo's Disease Wernicke Encephalopathy