Medical Subject Headings
MeSH Tree Structures - 2010
C10 - Nervous System Diseases
- Nervous System Diseases [C10]
- Autoimmune Diseases of the Nervous System [C10.114]
- Demyelinating Autoimmune Diseases, CNS [C10.114.375]
- Lambert-Eaton Myasthenic Syndrome [C10.114.468]
- Leukoencephalitis, Acute Hemorrhagic [C10.114.562]
- Myasthenia Gravis [C10.114.656]
- Nervous System Autoimmune Disease, Experimental [C10.114.703]
- Polyradiculoneuropathy [C10.114.750]
- Stiff-Person Syndrome [C10.114.812]
- Uveomeningoencephalitic Syndrome [C10.114.843]
- Vasculitis, Central Nervous System [C10.114.875]
- Autonomic Nervous System Diseases [C10.177]
- Adie Syndrome [C10.177.045]
- Autonomic Dysreflexia [C10.177.090]
- Complex Regional Pain Syndromes [C10.177.195]
- Horner Syndrome [C10.177.350]
- Primary Dysautonomias [C10.177.575]
- Sweating, Gustatory [C10.177.825]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Akinetic Mutism [C10.228.140.042]
- Amblyopia [C10.228.140.055]
- Amnesia, Transient Global [C10.228.140.060]
- Auditory Diseases, Central [C10.228.140.068]
- Basal Ganglia Diseases [C10.228.140.079]
- Basal Ganglia Cerebrovascular Disease [C10.228.140.079.127]
- Chorea Gravidarum [C10.228.140.079.294]
- Dystonia Musculorum Deformans [C10.228.140.079.357]
- Hepatolenticular Degeneration [C10.228.140.079.493]
- Pantothenate Kinase-Associated Neurodegeneration [C10.228.140.079.501]
- Huntington Disease [C10.228.140.079.545]
- Meige Syndrome [C10.228.140.079.590]
- Multiple System Atrophy [C10.228.140.079.612]
- Neuroleptic Malignant Syndrome [C10.228.140.079.737]
- Parkinsonian Disorders [C10.228.140.079.862]
- Supranuclear Palsy, Progressive [C10.228.140.079.882]
- Tourette Syndrome [C10.228.140.079.898]
- Brain Abscess [C10.228.140.116]
- Brain Damage, Chronic [C10.228.140.140]
- Brain Death [C10.228.140.151]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
- Galactosemias [C10.228.140.163.100.320]
- Hartnup Disease [C10.228.140.163.100.355]
- Hepatolenticular Degeneration [C10.228.140.163.100.360]
- Homocystinuria [C10.228.140.163.100.365]
- Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
- Hyperlysinemias [C10.228.140.163.100.380]
- Leigh Disease [C10.228.140.163.100.412]
- Lesch-Nyhan Syndrome [C10.228.140.163.100.425]
- Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
- Fucosidosis [C10.228.140.163.100.435.295]
- Glycogen Storage Disease Type II [C10.228.140.163.100.435.340]
- Mucolipidoses [C10.228.140.163.100.435.590]
- Sialic Acid Storage Disease [C10.228.140.163.100.435.810]
- Sphingolipidoses [C10.228.140.163.100.435.825]
- Fabry Disease [C10.228.140.163.100.435.825.200]
- Farber Lipogranulomatosis [C10.228.140.163.100.435.825.250]
- Gangliosidoses [C10.228.140.163.100.435.825.300]
- Gaucher Disease [C10.228.140.163.100.435.825.400]
- Leukodystrophy, Globoid Cell [C10.228.140.163.100.435.825.590]
- Niemann-Pick Diseases [C10.228.140.163.100.435.825.700]
- Sea-Blue Histiocyte Syndrome [C10.228.140.163.100.435.825.775]
- Sulfatidosis [C10.228.140.163.100.435.825.850]
- Maple Syrup Urine Disease [C10.228.140.163.100.520]
- MELAS Syndrome [C10.228.140.163.100.535]
- Menkes Kinky Hair Syndrome [C10.228.140.163.100.540]
- MERRF Syndrome [C10.228.140.163.100.545]
- Oculocerebrorenal Syndrome [C10.228.140.163.100.640]
- Peroxisomal Disorders [C10.228.140.163.100.680]
- Phenylketonurias [C10.228.140.163.100.687]
- Pyruvate Carboxylase Deficiency Disease [C10.228.140.163.100.725]
- Pyruvate Dehydrogenase Complex Deficiency Disease [C10.228.140.163.100.750]
- Tyrosinemias [C10.228.140.163.100.875]
- Urea Cycle Disorders, Inborn [C10.228.140.163.100.937]
- Argininosuccinic Aciduria [C10.228.140.163.100.937.124]
- Carbamoyl-Phosphate Synthase I Deficiency Disease [C10.228.140.163.100.937.249]
- Citrullinemia [C10.228.140.163.100.937.374]
- Hyperargininemia [C10.228.140.163.100.937.500]
- Ornithine Carbamoyltransferase Deficiency Disease [C10.228.140.163.100.937.750]
- Hepatic Encephalopathy [C10.228.140.163.360]
- Kernicterus [C10.228.140.163.480]
- Marchiafava-Bignami Disease [C10.228.140.163.510]
- Mitochondrial Encephalomyopathies [C10.228.140.163.540]
- Myelinolysis, Central Pontine [C10.228.140.163.560]
- Reye Syndrome [C10.228.140.163.780]
- Wernicke Encephalopathy [C10.228.140.163.960]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Brain Edema [C10.228.140.187]
- Brain Injuries [C10.228.140.199]
- Brain Neoplasms [C10.228.140.211]
- Cerebellar Diseases [C10.228.140.252]
- Cerebrovascular Disorders [C10.228.140.300]
- Basal Ganglia Cerebrovascular Disease [C10.228.140.300.100]
- Brain Ischemia [C10.228.140.300.150]
- Carotid Artery Diseases [C10.228.140.300.200]
- Carotid Artery Injuries [C10.228.140.300.200.345]
- Carotid Artery, Internal, Dissection [C10.228.140.300.200.353]
- Carotid Artery Thrombosis [C10.228.140.300.200.355]
- Carotid-Cavernous Sinus Fistula [C10.228.140.300.200.357]
- Carotid Stenosis [C10.228.140.300.200.360]
- Moyamoya Disease [C10.228.140.300.200.600]
- Cerebrovascular Trauma [C10.228.140.300.350]
- Dementia, Vascular [C10.228.140.300.400]
- Intracranial Arterial Diseases [C10.228.140.300.510]
- Cerebral Arterial Diseases [C10.228.140.300.510.200]
- CADASIL [C10.228.140.300.510.200.175]
- Cerebral Amyloid Angiopathy [C10.228.140.300.510.200.200]
- Infarction, Anterior Cerebral Artery [C10.228.140.300.510.200.325]
- Infarction, Middle Cerebral Artery [C10.228.140.300.510.200.387]
- Infarction, Posterior Cerebral Artery [C10.228.140.300.510.200.418]
- Moyamoya Disease [C10.228.140.300.510.200.737]
- Intracranial Aneurysm [C10.228.140.300.510.600]
- Intracranial Arteriosclerosis [C10.228.140.300.510.800]
- Cerebral Arterial Diseases [C10.228.140.300.510.200]
- Intracranial Arteriovenous Malformations [C10.228.140.300.520]
- Intracranial Embolism and Thrombosis [C10.228.140.300.525]
- Intracranial Hemorrhages [C10.228.140.300.535]
- Cerebral Hemorrhage [C10.228.140.300.535.200]
- Intracranial Hemorrhage, Hypertensive [C10.228.140.300.535.325]
- Intracranial Hemorrhage, Traumatic [C10.228.140.300.535.450]
- Pituitary Apoplexy [C10.228.140.300.535.625]
- Subarachnoid Hemorrhage [C10.228.140.300.535.800]
- Leukomalacia, Periventricular [C10.228.140.300.700]
- Sneddon Syndrome [C10.228.140.300.750]
- Stroke [C10.228.140.300.775]
- Susac Syndrome [C10.228.140.300.787]
- Vascular Headaches [C10.228.140.300.800]
- Vasculitis, Central Nervous System [C10.228.140.300.850]
- Vasospasm, Intracranial [C10.228.140.300.900]
- Vertebral Artery Dissection [C10.228.140.300.950]
- Dementia [C10.228.140.380]
- AIDS Dementia Complex [C10.228.140.380.070]
- Alzheimer Disease [C10.228.140.380.100]
- Aphasia, Primary Progressive [C10.228.140.380.132]
- Creutzfeldt-Jakob Syndrome [C10.228.140.380.165]
- Dementia, Vascular [C10.228.140.380.230]
- Diffuse Neurofibrillary Tangles with Calcification [C10.228.140.380.254]
- Frontotemporal Lobar Degeneration [C10.228.140.380.266]
- Huntington Disease [C10.228.140.380.278]
- Kluver-Bucy Syndrome [C10.228.140.380.326]
- Lewy Body Disease [C10.228.140.380.422]
- Pick Disease of the Brain [C10.228.140.380.615]
- Diffuse Cerebral Sclerosis of Schilder [C10.228.140.400]
- Encephalitis [C10.228.140.430]
- Encephalomalacia [C10.228.140.461]
- Epilepsy [C10.228.140.490]
- Epilepsies, Myoclonic [C10.228.140.490.250]
- Epilepsies, Partial [C10.228.140.490.360]
- Epilepsy, Benign Neonatal [C10.228.140.490.370]
- Epilepsy, Generalized [C10.228.140.490.375]
- Epilepsy, Post-Traumatic [C10.228.140.490.380]
- Epilepsy, Reflex [C10.228.140.490.450]
- Landau-Kleffner Syndrome [C10.228.140.490.535]
- Seizures [C10.228.140.490.631]
- Seizures, Febrile [C10.228.140.490.650]
- Status Epilepticus [C10.228.140.490.690]
- Headache Disorders [C10.228.140.546]
- Hydrocephalus [C10.228.140.602]
- Hypothalamic Diseases [C10.228.140.617]
- Bardet-Biedl Syndrome [C10.228.140.617.200]
- Hypothalamic Neoplasms [C10.228.140.617.477]
- Laurence-Moon Syndrome [C10.228.140.617.500]
- Pituitary Diseases [C10.228.140.617.738]
- Hypoxia, Brain [C10.228.140.624]
- Intracranial Hypertension [C10.228.140.631]
- Intracranial Hypotension [C10.228.140.638]
- Kluver-Bucy Syndrome [C10.228.140.646]
- Leukoencephalopathies [C10.228.140.695]
- Neuroaxonal Dystrophies [C10.228.140.744]
- Subdural Effusion [C10.228.140.870]
- Thalamic Diseases [C10.228.140.915]
- Central Nervous System Infections [C10.228.228]
- Brain Abscess [C10.228.228.090]
- Central Nervous System Bacterial Infections [C10.228.228.180]
- Brain Abscess [C10.228.228.180.100]
- Empyema, Subdural [C10.228.228.180.350]
- Epidural Abscess [C10.228.228.180.375]
- Lyme Neuroborreliosis [C10.228.228.180.437]
- Meningitis, Bacterial [C10.228.228.180.500]
- Neurosyphilis [C10.228.228.180.600]
- Tuberculosis, Central Nervous System [C10.228.228.180.850]
- Central Nervous System Fungal Infections [C10.228.228.198]
- Central Nervous System Parasitic Infections [C10.228.228.205]
- Central Nervous System Viral Diseases [C10.228.228.210]
- Encephalitis [C10.228.228.210.150]
- Encephalitis, Viral [C10.228.228.210.150.300]
- Encephalitis, Arbovirus [C10.228.228.210.150.300.300]
- Encephalitis, Herpes Simplex [C10.228.228.210.150.300.350]
- Encephalitis, Varicella Zoster [C10.228.228.210.150.300.400]
- Encephalomyelitis, Equine [C10.228.228.210.150.300.450]
- Leukoencephalopathy, Progressive Multifocal [C10.228.228.210.150.300.500]
- Subacute Sclerosing Panencephalitis [C10.228.228.210.150.300.600]
- Encephalitis, Viral [C10.228.228.210.150.300]
- Meningitis, Viral [C10.228.228.210.500]
- Myelitis [C10.228.228.210.575]
- Poliomyelitis [C10.228.228.210.650]
- Pseudorabies [C10.228.228.210.710]
- Encephalitis [C10.228.228.210.150]
- Empyema, Subdural [C10.228.228.227]
- Encephalitis [C10.228.228.245]
- Encephalitis, Viral [C10.228.228.245.340]
- Encephalitis, Arbovirus [C10.228.228.245.340.310]
- Encephalitis, Herpes Simplex [C10.228.228.245.340.332]
- Encephalitis, Varicella Zoster [C10.228.228.245.340.355]
- Encephalomyelitis, Equine [C10.228.228.245.340.450]
- Leukoencephalopathy, Progressive Multifocal [C10.228.228.245.340.575]
- Subacute Sclerosing Panencephalitis [C10.228.228.245.340.700]
- Meningoencephalitis [C10.228.228.245.550]
- Leukoencephalitis, Acute Hemorrhagic [C10.228.228.245.670]
- Limbic Encephalitis [C10.228.228.245.700]
- Encephalitis, Viral [C10.228.228.245.340]
- Encephalomyelitis [C10.228.228.291]
- Epidural Abscess [C10.228.228.300]
- Meningitis [C10.228.228.507]
- Arachnoiditis [C10.228.228.507.097]
- Meningitis, Aseptic [C10.228.228.507.220]
- Meningitis, Bacterial [C10.228.228.507.280]
- Meningitis, Fungal [C10.228.228.507.400]
- Meningitis, Viral [C10.228.228.507.700]
- Meningoencephalitis [C10.228.228.507.850]
- Meningoencephalitis [C10.228.228.553]
- Myelitis [C10.228.228.618]
- Perimeningeal Infections [C10.228.228.709]
- Prion Diseases [C10.228.228.800]
- Creutzfeldt-Jakob Syndrome [C10.228.228.800.230]
- Encephalopathy, Bovine Spongiform [C10.228.228.800.260]
- Gerstmann-Straussler-Scheinker Disease [C10.228.228.800.350]
- Insomnia, Fatal Familial [C10.228.228.800.392]
- Kuru [C10.228.228.800.435]
- Scrapie [C10.228.228.800.717]
- Wasting Disease, Chronic [C10.228.228.800.858]
- Encephalomyelitis [C10.228.440]
- High Pressure Neurological Syndrome [C10.228.470]
- Meningitis [C10.228.566]
- Movement Disorders [C10.228.662]
- Akathisia, Drug-Induced [C10.228.662.037]
- Angelman Syndrome [C10.228.662.075]
- Dyskinesias [C10.228.662.262]
- Dystonic Disorders [C10.228.662.300]
- Essential Tremor [C10.228.662.350]
- Hepatolenticular Degeneration [C10.228.662.400]
- Pantothenate Kinase-Associated Neurodegeneration [C10.228.662.425]
- Multiple System Atrophy [C10.228.662.550]
- Parkinsonian Disorders [C10.228.662.600]
- Supranuclear Palsy, Progressive [C10.228.662.700]
- Tic Disorders [C10.228.662.825]
- Ocular Motility Disorders [C10.228.758]
- Pneumocephalus [C10.228.806]
- Spinal Cord Diseases [C10.228.854]
- Amyotrophic Lateral Sclerosis [C10.228.854.139]
- Epidural Abscess [C10.228.854.303]
- Muscular Atrophy, Spinal [C10.228.854.468]
- Myelitis [C10.228.854.525]
- Poliomyelitis [C10.228.854.641]
- Spinal Cord Compression [C10.228.854.761]
- Spinal Cord Neoplasms [C10.228.854.765]
- Spinal Cord Injuries [C10.228.854.770]
- Spinal Cord Vascular Diseases [C10.228.854.785]
- Spinocerebellar Degenerations [C10.228.854.787]
- Stiff-Person Syndrome [C10.228.854.790]
- Subacute Combined Degeneration [C10.228.854.811]
- Syringomyelia [C10.228.854.833]
- Tabes Dorsalis [C10.228.854.889]
- Brain Diseases [C10.228.140]
- Chronobiology Disorders [C10.281]
- Cranial Nerve Diseases [C10.292]
- Abducens Nerve Diseases [C10.292.150]
- Accessory Nerve Diseases [C10.292.175]
- Cranial Nerve Neoplasms [C10.292.225]
- Cranial Nerve Injuries [C10.292.262]
- Facial Nerve Diseases [C10.292.300]
- Facial Neuralgia [C10.292.375]
- Glossopharyngeal Nerve Diseases [C10.292.450]
- Hypoglossal Nerve Diseases [C10.292.525]
- Ocular Motility Disorders [C10.292.562]
- Duane Retraction Syndrome [C10.292.562.250]
- Miller Fisher Syndrome [C10.292.562.350]
- Nystagmus, Pathologic [C10.292.562.675]
- Oculomotor Nerve Diseases [C10.292.562.700]
- Ophthalmoplegia [C10.292.562.750]
- Ophthalmoplegia, Chronic Progressive External [C10.292.562.775]
- Opsoclonus-Myoclonus Syndrome [C10.292.562.831]
- Strabismus [C10.292.562.887]
- Tolosa-Hunt Syndrome [C10.292.562.900]
- Oculomotor Nerve Diseases [C10.292.600]
- Olfactory Nerve Diseases [C10.292.650]
- Optic Nerve Diseases [C10.292.700]
- Trigeminal Nerve Diseases [C10.292.775]
- Trochlear Nerve Diseases [C10.292.850]
- Vagus Nerve Diseases [C10.292.887]
- Vestibulocochlear Nerve Diseases [C10.292.910]
- Demyelinating Diseases [C10.314]
- Demyelinating Autoimmune Diseases, CNS [C10.314.350]
- Diffuse Cerebral Sclerosis of Schilder [C10.314.350.112]
- Encephalomyelitis, Acute Disseminated [C10.314.350.225]
- Encephalomyelitis, Autoimmune, Experimental [C10.314.350.250]
- Leukoencephalitis, Acute Hemorrhagic [C10.314.350.375]
- Multiple Sclerosis [C10.314.350.500]
- Myelitis, Transverse [C10.314.350.600]
- Neuromyelitis Optica [C10.314.350.650]
- Hereditary Central Nervous System Demyelinating Diseases [C10.314.400]
- Leukoencephalopathy, Progressive Multifocal [C10.314.450]
- Marchiafava-Bignami Disease [C10.314.475]
- Myelinolysis, Central Pontine [C10.314.500]
- Polyradiculoneuropathy [C10.314.750]
- Subacute Combined Degeneration [C10.314.875]
- Demyelinating Autoimmune Diseases, CNS [C10.314.350]
- Nervous System Malformations [C10.500]
- Acrocallosal Syndrome [C10.500.070]
- Central Nervous System Cysts [C10.500.142]
- Central Nervous System Vascular Malformations [C10.500.190]
- Dandy-Walker Syndrome [C10.500.205]
- Hereditary Sensory and Motor Neuropathy [C10.500.300]
- Hereditary Sensory and Autonomic Neuropathies [C10.500.310]
- Holoprosencephaly [C10.500.410]
- Hydranencephaly [C10.500.450]
- Malformations of Cortical Development [C10.500.507]
- Neural Tube Defects [C10.500.680]
- Septo-Optic Dysplasia [C10.500.840]
- Nervous System Neoplasms [C10.551]
- Central Nervous System Neoplasms [C10.551.240]
- Brain Neoplasms [C10.551.240.250]
- Central Nervous System Cysts [C10.551.240.375]
- Meningeal Neoplasms [C10.551.240.500]
- Spinal Cord Neoplasms [C10.551.240.750]
- Cranial Nerve Neoplasms [C10.551.360]
- Neuroma, Acoustic [C10.551.525]
- Peripheral Nervous System Neoplasms [C10.551.775]
- Central Nervous System Neoplasms [C10.551.240]
- Neurocutaneous Syndromes [C10.562]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Alexander Disease [C10.574.500.024]
- Amyloid Neuropathies, Familial [C10.574.500.050]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175]
- Canavan Disease [C10.574.500.300]
- Cockayne Syndrome [C10.574.500.362]
- Dystonia Musculorum Deformans [C10.574.500.393]
- Gerstmann-Straussler-Scheinker Disease [C10.574.500.425]
- Hepatolenticular Degeneration [C10.574.500.487]
- Pantothenate Kinase-Associated Neurodegeneration [C10.574.500.492]
- Hereditary Central Nervous System Demyelinating Diseases [C10.574.500.494]
- Hereditary Sensory and Motor Neuropathy [C10.574.500.495]
- Hereditary Sensory and Autonomic Neuropathies [C10.574.500.496]
- Huntington Disease [C10.574.500.497]
- Lafora Disease [C10.574.500.529]
- Lesch-Nyhan Syndrome [C10.574.500.536]
- Menkes Kinky Hair Syndrome [C10.574.500.540]
- Myotonia Congenita [C10.574.500.545]
- Myotonic Dystrophy [C10.574.500.547]
- Neurofibromatoses [C10.574.500.549]
- Neuronal Ceroid-Lipofuscinoses [C10.574.500.550]
- Optic Atrophies, Hereditary [C10.574.500.662]
- Rett Syndrome [C10.574.500.775]
- Spinal Muscular Atrophies of Childhood [C10.574.500.812]
- Spinocerebellar Degenerations [C10.574.500.825]
- Tourette Syndrome [C10.574.500.850]
- Tuberous Sclerosis [C10.574.500.865]
- Unverricht-Lundborg Syndrome [C10.574.500.875]
- Lewy Body Disease [C10.574.531]
- Motor Neuron Disease [C10.574.562]
- Multiple System Atrophy [C10.574.625]
- Olivopontocerebellar Atrophies [C10.574.750]
- Paraneoplastic Syndromes, Nervous System [C10.574.781]
- Parkinson Disease [C10.574.812]
- Postpoliomyelitis Syndrome [C10.574.827]
- Prion Diseases [C10.574.843]
- Shy-Drager Syndrome [C10.574.875]
- Subacute Combined Degeneration [C10.574.910]
- Tauopathies [C10.574.945]
- TDP-43 Proteinopathies [C10.574.950]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Neurologic Manifestations [C10.597]
- Cerebrospinal Fluid Otorrhea [C10.597.230]
- Cerebrospinal Fluid Rhinorrhea [C10.597.267]
- Decerebrate State [C10.597.305]
- Dyskinesias [C10.597.350]
- Ataxia [C10.597.350.090]
- Athetosis [C10.597.350.110]
- Catalepsy [C10.597.350.200]
- Chorea [C10.597.350.250]
- Dystonia [C10.597.350.300]
- Hyperkinesis [C10.597.350.350]
- Hypokinesia [C10.597.350.400]
- Myoclonus [C10.597.350.500]
- Psychomotor Agitation [C10.597.350.600]
- Synkinesis [C10.597.350.675]
- Tics [C10.597.350.700]
- Tremor [C10.597.350.850]
- Gait Disorders, Neurologic [C10.597.404]
- Meningism [C10.597.544]
- Neurobehavioral Manifestations [C10.597.606]
- Catatonia [C10.597.606.115]
- Communication Disorders [C10.597.606.150]
- Language Disorders [C10.597.606.150.500]
- Agraphia [C10.597.606.150.500.050]
- Anomia [C10.597.606.150.500.090]
- Dyslexia [C10.597.606.150.500.300]
- Language Development Disorders [C10.597.606.150.500.550]
- Speech Disorders [C10.597.606.150.500.800]
- Learning Disorders [C10.597.606.150.550]
- Language Disorders [C10.597.606.150.500]
- Confusion [C10.597.606.337]
- Consciousness Disorders [C10.597.606.358]
- Lethargy [C10.597.606.441]
- Memory Disorders [C10.597.606.525]
- Mental Retardation [C10.597.606.643]
- Cri-du-Chat Syndrome [C10.597.606.643.180]
- De Lange Syndrome [C10.597.606.643.210]
- Down Syndrome [C10.597.606.643.220]
- Mental Retardation, X-Linked [C10.597.606.643.455]
- Adrenoleukodystrophy [C10.597.606.643.455.124]
- Coffin-Lowry Syndrome [C10.597.606.643.455.249]
- Fragile X Syndrome [C10.597.606.643.455.500]
- Glycogen Storage Disease Type IIb [C10.597.606.643.455.562]
- Lesch-Nyhan Syndrome [C10.597.606.643.455.625]
- Menkes Kinky Hair Syndrome [C10.597.606.643.455.687]
- Mucopolysaccharidosis II [C10.597.606.643.455.750]
- Pyruvate Dehydrogenase Complex Deficiency Disease [C10.597.606.643.455.875]
- Rett Syndrome [C10.597.606.643.455.937]
- Prader-Willi Syndrome [C10.597.606.643.690]
- Rubinstein-Taybi Syndrome [C10.597.606.643.700]
- WAGR Syndrome [C10.597.606.643.969]
- Williams Syndrome [C10.597.606.643.970]
- Perceptual Disorders [C10.597.606.762]
- Psychomotor Disorders [C10.597.606.881]
- Neurogenic Inflammation [C10.597.609]
- Neuromuscular Manifestations [C10.597.613]
- Pain [C10.597.617]
- Back Pain [C10.597.617.152]
- Facial Pain [C10.597.617.364]
- Headache [C10.597.617.470]
- Labor Pain [C10.597.617.515]
- Metatarsalgia [C10.597.617.560]
- Neck Pain [C10.597.617.576]
- Neuralgia [C10.597.617.682]
- Pain, Intractable [C10.597.617.788]
- Pain, Referred [C10.597.617.894]
- Slit Ventricle Syndrome [C10.597.617.947]
- Paralysis [C10.597.622]
- Paresis [C10.597.636]
- Pupil Disorders [C10.597.690]
- Reflex, Abnormal [C10.597.704]
- Seizures [C10.597.742]
- Sensation Disorders [C10.597.751]
- Dizziness [C10.597.751.237]
- Hearing Disorders [C10.597.751.418]
- Hearing Loss [C10.597.751.418.341]
- Deafness [C10.597.751.418.341.186]
- Hearing Loss, Bilateral [C10.597.751.418.341.374]
- Hearing Loss, Conductive [C10.597.751.418.341.562]
- Hearing Loss, Functional [C10.597.751.418.341.750]
- Hearing Loss, High-Frequency [C10.597.751.418.341.812]
- Hearing Loss, Mixed Conductive-Sensorineural [C10.597.751.418.341.849]
- Hearing Loss, Sensorineural [C10.597.751.418.341.887]
- Hearing Loss, Sudden [C10.597.751.418.341.900]
- Hearing Loss, Unilateral [C10.597.751.418.341.950]
- Hyperacusis [C10.597.751.418.505]
- Tinnitus [C10.597.751.418.670]
- Hearing Loss [C10.597.751.418.341]
- Olfaction Disorders [C10.597.751.600]
- Somatosensory Disorders [C10.597.751.791]
- Taste Disorders [C10.597.751.861]
- Vision Disorders [C10.597.751.941]
- Susac Syndrome [C10.597.825]
- Urinary Bladder, Neurogenic [C10.597.900]
- Vertigo [C10.597.951]
- Voice Disorders [C10.597.975]
- Neuromuscular Diseases [C10.668]
- Fatigue Syndrome, Chronic [C10.668.364]
- Isaacs Syndrome [C10.668.402]
- Motor Neuron Disease [C10.668.460]
- Muscular Atrophy, Spinal [C10.668.475]
- Muscular Diseases [C10.668.491]
- Muscular Disorders, Atrophic [C10.668.491.175]
- Muscular Dystrophies [C10.668.491.175.500]
- Distal Myopathies [C10.668.491.175.500.074]
- Muscular Dystrophies, Limb-Girdle [C10.668.491.175.500.149]
- Muscular Dystrophy, Duchenne [C10.668.491.175.500.300]
- Muscular Dystrophy, Emery-Dreifuss [C10.668.491.175.500.350]
- Muscular Dystrophy, Facioscapulohumeral [C10.668.491.175.500.400]
- Muscular Dystrophy, Oculopharyngeal [C10.668.491.175.500.450]
- Myotonic Dystrophy [C10.668.491.175.500.500]
- Postpoliomyelitis Syndrome [C10.668.491.175.750]
- Muscular Dystrophies [C10.668.491.175.500]
- Eosinophilia-Myalgia Syndrome [C10.668.491.387]
- Fibromyalgia [C10.668.491.425]
- Mitochondrial Myopathies [C10.668.491.500]
- Myopathies, Structural, Congenital [C10.668.491.550]
- Myositis [C10.668.491.562]
- Myotonic Disorders [C10.668.491.606]
- Paralyses, Familial Periodic [C10.668.491.650]
- Muscular Disorders, Atrophic [C10.668.491.175]
- Muscular Disorders, Atrophic [C10.668.550]
- Neuromuscular Junction Diseases [C10.668.758]
- Peripheral Nervous System Diseases [C10.668.829]
- Acrodynia [C10.668.829.025]
- Amyloid Neuropathies [C10.668.829.050]
- Brachial Plexus Neuropathies [C10.668.829.100]
- Complex Regional Pain Syndromes [C10.668.829.250]
- Diabetic Neuropathies [C10.668.829.300]
- Giant Axonal Neuropathy [C10.668.829.325]
- Guillain-Barre Syndrome [C10.668.829.350]
- Hand-Arm Vibration Syndrome [C10.668.829.380]
- Isaacs Syndrome [C10.668.829.425]
- Mononeuropathies [C10.668.829.500]
- Nerve Compression Syndromes [C10.668.829.550]
- Neuralgia [C10.668.829.600]
- Neuritis [C10.668.829.650]
- Neurofibromatosis 1 [C10.668.829.675]
- Pain Insensitivity, Congenital [C10.668.829.700]
- Peripheral Nervous System Neoplasms [C10.668.829.725]
- Polyneuropathies [C10.668.829.800]
- Alcoholic Neuropathy [C10.668.829.800.050]
- Hereditary Sensory and Motor Neuropathy [C10.668.829.800.300]
- Hereditary Sensory and Autonomic Neuropathies [C10.668.829.800.625]
- Paraneoplastic Polyneuropathy [C10.668.829.800.662]
- POEMS Syndrome [C10.668.829.800.700]
- Polyradiculoneuropathy [C10.668.829.800.750]
- Tangier Disease [C10.668.829.800.875]
- Radiculopathy [C10.668.829.820]
- Tarlov Cysts [C10.668.829.900]
- Stiff-Person Syndrome [C10.668.900]
- Neurotoxicity Syndromes [C10.720]
- Akathisia, Drug-Induced [C10.720.075]
- Alcohol-Induced Disorders, Nervous System [C10.720.112]
- Botulism [C10.720.150]
- Dyskinesia, Drug-Induced [C10.720.312]
- Heavy Metal Poisoning, Nervous System [C10.720.475]
- MPTP Poisoning [C10.720.606]
- Neuroleptic Malignant Syndrome [C10.720.737]
- Sleep Disorders [C10.886]
- Dyssomnias [C10.886.425]
- Sleep Deprivation [C10.886.425.175]
- Sleep Disorders, Circadian Rhythm [C10.886.425.200]
- Sleep Disorders, Intrinsic [C10.886.425.800]
- Parasomnias [C10.886.659]
- Dyssomnias [C10.886.425]
- Trauma, Nervous System [C10.900]
- Cerebrovascular Trauma [C10.900.250]
- Craniocerebral Trauma [C10.900.300]
- Brain Injuries [C10.900.300.087]
- Cerebrospinal Fluid Otorrhea [C10.900.300.131]
- Cerebrospinal Fluid Rhinorrhea [C10.900.300.153]
- Coma, Post-Head Injury [C10.900.300.175]
- Cranial Nerve Injuries [C10.900.300.218]
- Head Injuries, Closed [C10.900.300.350]
- Head Injuries, Penetrating [C10.900.300.675]
- Intracranial Hemorrhage, Traumatic [C10.900.300.837]
- Skull Fractures [C10.900.300.918]
- Spinal Cord Injuries [C10.900.850]
- Autoimmune Diseases of the Nervous System [C10.114]
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U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894
National Institutes of Health, Health & Human Services
Freedom of Information Act, NLM Customer Support
