Informaţii despre

Nume Peripheral Nervous System Disease
Pagina Web www.malacards.org
Clasificari ICD10 Other disorders of peripheral nervous system
Clasificare anatomică Malacards Boli neuronale

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Boli A-Z 3-Methylglutaconic Aciduria, Type Iv Accommodative Esotropia Achromatopsia 2 Acquired Metabolic Disease Adie Pupil Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Esotropia Amblyopia Amyloid Tumor Amyotrophic Neuralgia Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Autonomic Nervous System Disease Autonomic Nervous System Neoplasm Autonomic Neuropathy Axonal Neuropathy Blood Group--Ahonen Brachial Plexus Neuritis Burning Mouth Syndrome Burns Carpal Tunnel Syndrome Cauda Equina Syndrome Celiac Disease 1 Cenani-Lenz Syndactyly Syndrome Central Pontine Myelinolysis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease and Deafness Charcot-Marie-Tooth Disease, Axonal, Type 2b Charcot-Marie-Tooth Disease, Axonal, Type 2e Charcot-Marie-Tooth Disease, Axonal, Type 2f Charcot-Marie-Tooth Disease, Axonal, Type 2k Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1c Charcot-Marie-Tooth Disease, Demyelinating, Type 1d Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Charcot-Marie-Tooth Disease, Type 4a Charcot-Marie-Tooth Disease, Type 4b1 Charcot-Marie-Tooth Disease, Type 4b2 Charcot-Marie-Tooth Disease, Type 4b3 Charcot-Marie-Tooth Disease, Type 4c Charcot-Marie-Tooth Disease, Type 4d Charcot-Marie-Tooth Disease, Type 4j Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 Charcot-Marie-Tooth Neuropathy Type 1 Chronic Polyneuropathy Complement Component 3 Deficiency, Autosomal Recessive Complex Regional Pain Syndrome Congenital Hypomyelination Neuropathy Congenital Myasthenic Syndrome Congenital Ptosis Cortical Blindness Cough Variant Asthma Cranial Nerve Disease Deafness, Autosomal Dominant 28 Demyelinating Polyneuropathy Diabetic Autonomic Neuropathy Diabetic Neuropathy Distal Arthrogryposis Duane Retraction Syndrome Encephalomyopathy Esotropia Exotropia Exposure Keratitis Facial Hemiatrophy Facial Nerve Disease Facial Paralysis Factitious Disorder Fetal Akinesia Deformation Sequence Foot Drop Geniculate Herpes Zoster Giant Axonal Neuropathy Glucose Metabolism Disease Guillain-Barre Syndrome Hansen's Disease Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hyperglycemia Hypertrophic Neuropathy of Dejerine-Sottas Hypertropia Hypotropia Immune System Disease Ischemia Jejunoileitis Juvenile Spinal Muscular Atrophy Kearns-Sayre Syndrome Krabbe Disease Leber Optic Atrophy Leber Optic Atrophy and Dystonia Lesion of Sciatic Nerve Leukodystrophy Miller Fisher Syndrome Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Monoclonal Gammopathy of Uncertain Significance Mononeuritis Multiplex Mononeuritis of Lower Limb Mononeuritis of Upper Limb and Mononeuritis Multiplex Mononeuropathy Mononeuropathy of the Median Nerve, Mild Motor Peripheral Neuropathy Multifocal Motor Neuropathy Neonatal Myasthenia Gravis Nerve Compression Syndrome Nervous System Disease Neuritis Neurogenic Arthropathy Neuromuscular Disease Neuromuscular Junction Disease Neuropathy Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive Neuropathy, Hereditary Motor and Sensory, Russe Type Neuropathy, Hereditary Sensory and Autonomic, Type Iia Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuropathy, Hereditary, with Liability to Pressure Palsies Niemann-Pick Disease, Type a Nutritional Deficiency Disease Ocular Motility Disease Oculomotor Nerve Paralysis Optic Nerve Disease Optic Neuritis Osteosclerotic Myeloma Paine Syndrome Panencephalitis, Subacute Sclerosing Paralytic Squint Paroxysmal Extreme Pain Disorder Pelizaeus-Merzbacher Disease Peripheral Nervous System Neoplasm Plasma Cell Neoplasm Plasma Protein Metabolism Disease Poikiloderma with Neutropenia Polyclonal Hypergammaglobulinemia Polyneuropathy Progressive Muscular Atrophy Ptosis Roussy-Levy Hereditary Areflexic Dystasia Sciatic Neuropathy Sclerosteosis 2 Sensory Peripheral Neuropathy Sick Building Syndrome Somatoform Disorder Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Strabismus Survival Motor Neuron Spinal Muscular Atrophy Third Cranial Nerve Disease Thoracic Outlet Syndrome Tooth Disease Trigeminal Nerve Disease Trigeminal Neuralgia Tukel Syndrome Ulnar Neuropathy