Informaţii despre

Nume Lateral Sclerosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Primary Lateral Sclerosis, Adult, 1; Primary Lateral Sclerosis, Juvenile

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Boli A-Z Ablepharon-Macrostomia Syndrome Acromegaly Adenoma Adie Pupil Aging Agraphia 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 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 8 Amyotrophic Lateral Sclerosis 9 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 6 Amyotrophy, Monomelic Aniridia 1 Anorexia Nervosa 1 Anosognosia Aphasia Apraxia Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Attention Deficit-Hyperactivity Disorder Autoimmune Disease Autonomic Dysfunction Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Black Hairy Tongue Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Borna Disease Brain Cancer Breast Cancer Brown-Vialetto-Van Laere Syndrome Bullous Pemphigoid C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Cardiac Arrest Cerebral Atrophy Cerebral Degeneration Cerebritis Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease Type 2a Cholecystitis Cholelithiasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Corticobasal Degeneration Dementia Demyelinating Polyneuropathy Diabetic Neuropathy Distal Hereditary Motor Neuropathies Down Syndrome Dyschromatosis Symmetrica Hereditaria Dysgraphia Dysphagia Dystonia Encephalopathy Endotheliitis Eosinophilic Fasciitis Epilepsy Epithelial Recurrent Erosion Dystrophy Essential Tremor 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 Genitopatellar Syndrome Gynecomastia Hairy Tongue Head Injury Hemiplegia Hepatic Adenomas, Familial Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Spastic Paraplegia Hyperparathyroidism Hyperphenylalaninemia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoparathyroidism Hypoxia Inclusion Body Myositis Infant Gynecomastia Insulin-Like Growth Factor I Juvenile Amyotrophic Lateral Sclerosis Kartagener Syndrome Klippel-Feil Syndrome Lathyrism Legius Syndrome Leukemia Liposarcoma Lyme Disease Macroglobulinemia Macroglossia Malignant Spiradenoma Meckel Syndrome, Type 1 Meningitis and Encephalitis Menkes Disease 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 Myositis Myotonic Dystrophy Nemaline Myopathy Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation Neuroendocrine Tumor Neurofibroma Neuromuscular Disease Neuromyelitis Optica Neuronitis Neuropathy Neurosarcoidosis Neurosyphilis Neutrophil Actin Dysfunction Nominal Aphasia Non-Involuting Congenital Hemangioma Obsessive-Compulsive Disorder Olivopontocerebellar Atrophy Opitz Gbbb Syndrome, Type Ii Papilloma Papillon-Lefevre Syndrome Paralytic Poliomyelitis Paraplegia Pathological Gambling Patulous Eustachian Tube Periodontitis, Aggressive, 1 Pituitary Adenoma Pleomorphic Liposarcoma Poems Syndrome Poliomyelitis Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polykaryocytosis Inducer Polymicrogyria Polyneuropathy Polyradiculoneuropathy Polyradiculopathy Pompholyx Postpoliomyelitis Syndrome Potocki-Lupski Syndrome Primary Lateral Sclerosis, Adult, 1 Primary Lateral Sclerosis, Juvenile Primary Progressive Multiple Sclerosis Prion Disease Progressive Muscular Atrophy Progressive Non-Fluent Aphasia Prostatitis Proximal Spinal Muscular Atrophy Pseudobulbar Palsy Pulmonary Alveolar Microlithiasis Reflex Sympathetic Dystrophy Renal Glucosuria Restless Legs Syndrome Retinitis Sarcoma Satb2-Associated Syndrome Schistosomiasis Schizophrenia Seizures, Benign Familial Neonatal, 1 Semantic Dementia Siderosis Sleep Apnea Spasmodic Dysphonia Spasticity Spastic Paraparesis Spastic Paraplegia 11 Spastic Paraplegia 35, Autosomal Recessive Speech Disorder Spinal Muscular Atrophy Spinocerebellar Ataxia 2 Split Hand Spondylosis Superficial Siderosis Superficial Siderosis of the Central Nervous System Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Tardbp-Related Amyotrophic Lateral Sclerosis Tetraamelia Syndrome, Autosomal Recessive Tooth Disease Tremor Tropical Spastic Paraparesis Variably Protease-Sensitive Prionopathy