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List of MeSH codes (C10)
Từ VLOS
- For other categories, see List of MeSH codes.
The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.
Source for content is here. (File "2006 MeSH Trees".)
Mục lục
-
1
MeSH
C10
---
nervous
system
diseases
-
1.1
MeSH
C10.114
---
autoimmune
diseases
of
the
nervous
system
- 1.1.1 MeSH C10.114.375 --- demyelinating autoimmune diseases, cns
- 1.1.2 MeSH C10.114.468 --- lambert-eaton myasthenic syndrome
- 1.1.3 MeSH C10.114.562 --- leukoencephalitis, acute hemorrhagic
- 1.1.4 MeSH C10.114.656 --- myasthenia gravis
- 1.1.5 MeSH C10.114.703 --- nervous system autoimmune disease, experimental
- 1.1.6 MeSH C10.114.750 --- polyradiculoneuropathy
- 1.1.7 MeSH C10.114.812 --- stiff-person syndrome
- 1.1.8 MeSH C10.114.843 --- uveomeningoencephalitic syndrome
- 1.1.9 MeSH C10.114.875 --- vasculitis, central nervous system
-
1.2
MeSH
C10.177
---
autonomic
nervous
system
diseases
- 1.2.1 MeSH C10.177.045 --- adie syndrome
- 1.2.2 MeSH C10.177.090 --- autonomic dysreflexia
- 1.2.3 MeSH C10.177.195 --- complex regional pain syndromes
- 1.2.4 MeSH C10.177.272 --- dysautonomia, familial
- 1.2.5 MeSH C10.177.350 --- horner syndrome
- 1.2.6 MeSH C10.177.800 --- shy-drager syndrome
- 1.2.7 MeSH C10.177.825 --- sweating, gustatory
-
1.3
MeSH
C10.228
---
central
nervous
system
diseases
- 1.3.1 MeSH C10.228.140 --- brain diseases
- 1.3.2 MeSH C10.228.228 --- central nervous system infections
- 1.3.3 MeSH C10.228.440 --- encephalomyelitis
- 1.3.4 MeSH C10.228.470 --- high pressure neurological syndrome
- 1.3.5 MeSH C10.228.566 --- meningitis
- 1.3.6 MeSH C10.228.662 --- movement disorders
- 1.3.7 MeSH C10.228.758 --- ocular motility disorders
- 1.3.8 MeSH C10.228.806 --- pneumocephalus
- 1.3.9 MeSH C10.228.854 --- spinal cord diseases
- 1.4 MeSH C10.281 --- chronobiology disorders
-
1.5
MeSH
C10.292
---
cranial
nerve
diseases
- 1.5.1 MeSH C10.292.150 --- abducens nerve diseases
- 1.5.2 MeSH C10.292.175 --- accessory nerve diseases
- 1.5.3 MeSH C10.292.225 --- cranial nerve neoplasms
- 1.5.4 MeSH C10.292.262 --- cranial nerve injuries
- 1.5.5 MeSH C10.292.300 --- facial nerve diseases
- 1.5.6 MeSH C10.292.375 --- facial neuralgia
- 1.5.7 MeSH C10.292.450 --- glossopharyngeal nerve diseases
- 1.5.8 MeSH C10.292.525 --- hypoglossal nerve diseases
- 1.5.9 MeSH C10.292.562 --- ocular motility disorders
- 1.5.10 MeSH C10.292.600 --- oculomotor nerve diseases
- 1.5.11 MeSH C10.292.650 --- olfactory nerve diseases
- 1.5.12 MeSH C10.292.700 --- optic nerve diseases
- 1.5.13 MeSH C10.292.775 --- trigeminal nerve diseases
- 1.5.14 MeSH C10.292.850 --- trochlear nerve diseases
- 1.5.15 MeSH C10.292.887 --- vagus nerve diseases
- 1.5.16 MeSH C10.292.910 --- vestibulocochlear nerve diseases
-
1.6
MeSH
C10.314
---
demyelinating
diseases
- 1.6.1 MeSH C10.314.350 --- demyelinating autoimmune diseases, cns
- 1.6.2 MeSH C10.314.400 --- hereditary central nervous system demyelinating diseases
- 1.6.3 MeSH C10.314.450 --- leukoencephalopathy, progressive multifocal
- 1.6.4 MeSH C10.314.500 --- myelinolysis, central pontine
- 1.6.5 MeSH C10.314.750 --- polyradiculoneuropathy
-
1.7
MeSH
C10.500
---
nervous
system
malformations
- 1.7.1 MeSH C10.500.142 --- central nervous system cysts
- 1.7.2 MeSH C10.500.190 --- central nervous system vascular malformations
- 1.7.3 MeSH C10.500.205 --- dandy-walker syndrome
- 1.7.4 MeSH C10.500.300 --- hereditary motor and sensory neuropathies
- 1.7.5 MeSH C10.500.310 --- hereditary sensory and autonomic neuropathies
- 1.7.6 MeSH C10.500.410 --- holoprosencephaly
- 1.7.7 MeSH C10.500.450 --- hydranencephaly
- 1.7.8 MeSH C10.500.460 --- intracranial arteriovenous malformations
- 1.7.9 MeSH C10.500.680 --- neural tube defects
- 1.7.10 MeSH C10.500.840 --- septo-optic dysplasia
- 1.8 MeSH C10.551 --- nervous system neoplasms
- 1.9 MeSH C10.562 --- neurocutaneous syndromes
-
1.10
MeSH
C10.574
---
neurodegenerative
diseases
- 1.10.1 MeSH C10.574.500 --- heredodegenerative disorders, nervous system
- 1.10.2 MeSH C10.574.531 --- lewy body disease
- 1.10.3 MeSH C10.574.562 --- motor neuron disease
- 1.10.4 MeSH C10.574.625 --- multiple system atrophy
- 1.10.5 MeSH C10.574.750 --- olivopontocerebellar atrophies
- 1.10.6 MeSH C10.574.781 --- paraneoplastic syndromes, nervous system
- 1.10.7 MeSH C10.574.812 --- parkinson disease
- 1.10.8 MeSH C10.574.827 --- postpoliomyelitis syndrome
- 1.10.9 MeSH C10.574.843 --- prion diseases
- 1.10.10 MeSH C10.574.875 --- shy-drager syndrome
- 1.10.11 MeSH C10.574.945 --- tauopathies
-
1.11
MeSH
C10.597
---
neurologic
manifestations
- 1.11.1 MeSH C10.597.200 --- bladder, neurogenic
- 1.11.2 MeSH C10.597.230 --- cerebrospinal fluid otorrhea
- 1.11.3 MeSH C10.597.267 --- cerebrospinal fluid rhinorrhea
- 1.11.4 MeSH C10.597.305 --- decerebrate state
- 1.11.5 MeSH C10.597.350 --- dyskinesias
- 1.11.6 MeSH C10.597.404 --- gait disorders, neurologic
- 1.11.7 MeSH C10.597.544 --- meningism
- 1.11.8 MeSH C10.597.606 --- neurobehavioral manifestations
- 1.11.9 MeSH C10.597.609 --- neurogenic inflammation
- 1.11.10 MeSH C10.597.613 --- neuromuscular manifestations
- 1.11.11 MeSH C10.597.617 --- pain
- 1.11.12 MeSH C10.597.622 --- paralysis
- 1.11.13 MeSH C10.597.636 --- paresis
- 1.11.14 MeSH C10.597.690 --- pupil disorders
- 1.11.15 MeSH C10.597.704 --- reflex, abnormal
- 1.11.16 MeSH C10.597.742 --- seizures
- 1.11.17 MeSH C10.597.751 --- sensation disorders
- 1.11.18 MeSH C10.597.951 --- vertigo
- 1.11.19 MeSH C10.597.975 --- voice disorders
-
1.12
MeSH
C10.668
---
neuromuscular
diseases
- 1.12.1 MeSH C10.668.364 --- fatigue syndrome, chronic
- 1.12.2 MeSH C10.668.402 --- isaacs syndrome
- 1.12.3 MeSH C10.668.460 --- motor neuron disease
- 1.12.4 MeSH C10.668.475 --- muscular atrophy, spinal
- 1.12.5 MeSH C10.668.491 --- muscular diseases
- 1.12.6 MeSH C10.668.550 --- muscular disorders, atrophic
- 1.12.7 MeSH C10.668.758 --- neuromuscular junction diseases
- 1.12.8 MeSH C10.668.829 --- peripheral nervous system diseases
- 1.12.9 MeSH C10.668.900 --- stiff-person syndrome
-
1.13
MeSH
C10.720
---
neurotoxicity
syndromes
- 1.13.1 MeSH C10.720.075 --- akathisia, drug-induced
- 1.13.2 MeSH C10.720.112 --- alcohol-induced disorders, nervous system
- 1.13.3 MeSH C10.720.150 --- botulism
- 1.13.4 MeSH C10.720.312 --- dyskinesia, drug-induced
- 1.13.5 MeSH C10.720.475 --- heavy metal poisoning, nervous system
- 1.13.6 MeSH C10.720.606 --- mptp poisoning
- 1.13.7 MeSH C10.720.737 --- neuroleptic malignant syndrome
- 1.14 MeSH C10.886 --- sleep disorders
- 1.15 MeSH C10.900 --- trauma, nervous system
-
1.1
MeSH
C10.114
---
autoimmune
diseases
of
the
nervous
system
MeSH C10 --- nervous system diseases[sửa]
MeSH C10.114 --- autoimmune diseases of the nervous system[sửa]
MeSH C10.114.375 --- demyelinating autoimmune diseases, cns[sửa]
- MeSH C10.114.375.112 --- diffuse cerebral sclerosis of schilder
- MeSH C10.114.375.225 --- encephalomyelitis, acute disseminated
- MeSH C10.114.375.362 --- leukoencephalitis, acute hemorrhagic
- MeSH C10.114.375.500 --- multiple sclerosis
- MeSH C10.114.375.500.200 --- multiple sclerosis, chronic progressive
- MeSH C10.114.375.500.600 --- multiple sclerosis, relapsing-remitting
- MeSH C10.114.375.500.650 --- neuromyelitis optica
- MeSH C10.114.375.600 --- myelitis, transverse
- MeSH C10.114.375.600.500 --- neuromyelitis optica
- MeSH C10.114.375.650 --- neuromyelitis optica
MeSH C10.114.468 --- lambert-eaton myasthenic syndrome[sửa]
MeSH C10.114.562 --- leukoencephalitis, acute hemorrhagic[sửa]
MeSH C10.114.656 --- myasthenia gravis[sửa]
- MeSH C10.114.656.300 --- myasthenia gravis, autoimmune, experimental
- MeSH C10.114.656.650 --- myasthenia gravis, neonatal
MeSH C10.114.703 --- nervous system autoimmune disease, experimental[sửa]
- MeSH C10.114.703.300 --- encephalomyelitis, autoimmune, experimental
- MeSH C10.114.703.350 --- myasthenia gravis, autoimmune, experimental
- MeSH C10.114.703.700 --- neuritis, autoimmune, experimental
MeSH C10.114.750 --- polyradiculoneuropathy[sửa]
- MeSH C10.114.750.100 --- guillain-barre syndrome
- MeSH C10.114.750.100.500 --- miller fisher syndrome
- MeSH C10.114.750.137 --- hereditary sensory and autonomic neuropathies
- MeSH C10.114.750.137.250 --- dysautonomia, familial
- MeSH C10.114.750.175 --- polyradiculoneuropathy, chronic inflammatory demyelinating
MeSH C10.114.812 --- stiff-person syndrome[sửa]
MeSH C10.114.843 --- uveomeningoencephalitic syndrome[sửa]
MeSH C10.114.875 --- vasculitis, central nervous system[sửa]
- MeSH C10.114.875.175 --- aids arteritis, central nervous system
- MeSH C10.114.875.350 --- lupus vasculitis, central nervous system
- MeSH C10.114.875.700 --- temporal arteritis
MeSH C10.177 --- autonomic nervous system diseases[sửa]
MeSH C10.177.045 --- adie syndrome[sửa]
MeSH C10.177.090 --- autonomic dysreflexia[sửa]
MeSH C10.177.195 --- complex regional pain syndromes[sửa]
MeSH C10.177.272 --- dysautonomia, familial[sửa]
MeSH C10.177.350 --- horner syndrome[sửa]
MeSH C10.177.800 --- shy-drager syndrome[sửa]
MeSH C10.177.825 --- sweating, gustatory[sửa]
MeSH C10.228 --- central nervous system diseases[sửa]
MeSH C10.228.140 --- brain diseases[sửa]
- MeSH C10.228.140.042 --- akinetic mutism
- MeSH C10.228.140.055 --- amblyopia
- MeSH C10.228.140.060 --- amnesia, transient global
- MeSH C10.228.140.068 --- auditory diseases, central
- MeSH C10.228.140.068.094 --- auditory perceptual disorders
- MeSH C10.228.140.068.432 --- hearing loss, central
- MeSH C10.228.140.079 --- basal ganglia diseases
- MeSH C10.228.140.079.127 --- basal ganglia cerebrovascular disease
- MeSH C10.228.140.079.127.500 --- basal ganglia hemorrhage
- MeSH C10.228.140.079.127.500.500 --- putaminal hemorrhage
- MeSH C10.228.140.079.294 --- chorea gravidarum
- MeSH C10.228.140.079.357 --- dystonia musculorum deformans
- MeSH C10.228.140.079.493 --- hallervorden-spatz syndrome
- MeSH C10.228.140.079.501 --- hepatolenticular degeneration
- MeSH C10.228.140.079.545 --- huntington disease
- MeSH C10.228.140.079.590 --- meige syndrome
- MeSH C10.228.140.079.612 --- multiple system atrophy
- MeSH C10.228.140.079.612.600 --- olivopontocerebellar atrophies
- MeSH C10.228.140.079.612.700 --- shy-drager syndrome
- MeSH C10.228.140.079.612.800 --- striatonigral degeneration
- MeSH C10.228.140.079.737 --- neuroleptic malignant syndrome
- MeSH C10.228.140.079.862 --- parkinsonian disorders
- MeSH C10.228.140.079.862.400 --- lewy body disease
- MeSH C10.228.140.079.862.500 --- parkinson disease
- MeSH C10.228.140.079.862.800 --- parkinson disease, secondary
- MeSH C10.228.140.079.862.800.300 --- mptp poisoning
- MeSH C10.228.140.079.862.800.600 --- parkinson disease, postencephalitic
- MeSH C10.228.140.079.882 --- supranuclear palsy, progressive
- MeSH C10.228.140.079.898 --- tourette syndrome
- MeSH C10.228.140.116 --- brain abscess
- MeSH C10.228.140.116.800 --- toxoplasmosis, cerebral
- MeSH C10.228.140.140 --- brain damage, chronic
- MeSH C10.228.140.140.127 --- brain injury, chronic
- MeSH C10.228.140.140.254 --- cerebral palsy
- MeSH C10.228.140.140.627 --- persistent vegetative state
- MeSH C10.228.140.151 --- brain death
- MeSH C10.228.140.163 --- brain diseases, metabolic
- MeSH C10.228.140.163.100 --- brain diseases, metabolic, inborn
- MeSH C10.228.140.163.100.050 --- abetalipoproteinemia
- MeSH C10.228.140.163.100.162 --- carbamoyl-phosphate synthase i deficiency disease
- MeSH C10.228.140.163.100.168 --- cerebral amyloid angiopathy, familial
- MeSH C10.228.140.163.100.175 --- citrullinemia
- MeSH C10.228.140.163.100.320 --- galactosemias
- MeSH C10.228.140.163.100.355 --- hartnup disease
- MeSH C10.228.140.163.100.360 --- hepatolenticular degeneration
- MeSH C10.228.140.163.100.365 --- homocystinuria
- MeSH C10.228.140.163.100.370 --- hyperargininemia
- MeSH C10.228.140.163.100.375 --- hyperglycinemia, nonketotic
- MeSH C10.228.140.163.100.380 --- hyperlysinemias
- MeSH C10.228.140.163.100.412 --- leigh disease
- MeSH C10.228.140.163.100.425 --- lesch-nyhan syndrome
- MeSH C10.228.140.163.100.435 --- lysosomal storage diseases, nervous system
- MeSH C10.228.140.163.100.435.295 --- fucosidosis
- MeSH C10.228.140.163.100.435.340 --- glycogen storage disease type ii
- MeSH C10.228.140.163.100.435.590 --- mucolipidoses
- MeSH C10.228.140.163.100.435.810 --- sialic acid storage disease
- MeSH C10.228.140.163.100.435.825 --- sphingolipidoses
- MeSH C10.228.140.163.100.435.825.200 --- fabry disease
- MeSH C10.228.140.163.100.435.825.300 --- gangliosidoses
- MeSH C10.228.140.163.100.435.825.300.300 --- gangliosidoses gm2
- MeSH C10.228.140.163.100.435.825.300.300.249 --- sandhoff disease
- MeSH C10.228.140.163.100.435.825.300.300.500 --- tay-sachs disease
- MeSH C10.228.140.163.100.435.825.300.300.750 --- tay-sachs disease, ab variant
- MeSH C10.228.140.163.100.435.825.300.400 --- gangliosidosis gm1
- MeSH C10.228.140.163.100.435.825.300.700 --- sandhoff disease
- MeSH C10.228.140.163.100.435.825.400 --- gaucher disease
- MeSH C10.228.140.163.100.435.825.590 --- leukodystrophy, globoid cell
- MeSH C10.228.140.163.100.435.825.594 --- leukodystrophy, metachromatic
- MeSH C10.228.140.163.100.435.825.700 --- niemann-pick diseases
- MeSH C10.228.140.163.100.520 --- maple syrup urine disease
- MeSH C10.228.140.163.100.535 --- melas syndrome
- MeSH C10.228.140.163.100.540 --- menkes kinky hair syndrome
- MeSH C10.228.140.163.100.545 --- merrf syndrome
- MeSH C10.228.140.163.100.640 --- oculocerebrorenal syndrome
- MeSH C10.228.140.163.100.650 --- ornithine carbamoyltransferase deficiency disease
- MeSH C10.228.140.163.100.680 --- peroxisomal disorders
- MeSH C10.228.140.163.100.680.100 --- adrenoleukodystrophy
- MeSH C10.228.140.163.100.680.760 --- refsum disease
- MeSH C10.228.140.163.100.680.970 --- zellweger syndrome
- MeSH C10.228.140.163.100.687 --- phenylketonurias
- MeSH C10.228.140.163.100.687.500 --- phenylketonuria, maternal
- MeSH C10.228.140.163.100.725 --- pyruvate carboxylase deficiency disease
- MeSH C10.228.140.163.100.750 --- pyruvate dehydrogenase complex deficiency disease
- MeSH C10.228.140.163.100.875 --- tyrosinemias
- MeSH C10.228.140.163.360 --- hepatic encephalopathy
- MeSH C10.228.140.163.480 --- kernicterus
- MeSH C10.228.140.163.540 --- mitochondrial encephalomyopathies
- MeSH C10.228.140.163.560 --- myelinolysis, central pontine
- MeSH C10.228.140.163.780 --- reye syndrome
- MeSH C10.228.140.163.960 --- wernicke encephalopathy
- MeSH C10.228.140.187 --- brain edema
- MeSH C10.228.140.199 --- brain injuries
- MeSH C10.228.140.199.250 --- brain concussion
- MeSH C10.228.140.199.250.500 --- post-concussion syndrome
- MeSH C10.228.140.199.275 --- brain hemorrhage, traumatic
- MeSH C10.228.140.199.275.200 --- brain stem hemorrhage, traumatic
- MeSH C10.228.140.199.275.300 --- cerebral hemorrhage, traumatic
- MeSH C10.228.140.199.500 --- brain injury, chronic
- MeSH C10.228.140.199.600 --- diffuse axonal injury
- MeSH C10.228.140.199.650 --- epilepsy, post-traumatic
- MeSH C10.228.140.199.700 --- pneumocephalus
- MeSH C10.228.140.211 --- brain neoplasms
- MeSH C10.228.140.211.280 --- cerebral ventricle neoplasms
- MeSH C10.228.140.211.280.300 --- choroid plexus neoplasms
- MeSH C10.228.140.211.280.300.500 --- papilloma, choroid plexus
- MeSH C10.228.140.211.500 --- infratentorial neoplasms
- MeSH C10.228.140.211.500.100 --- brain stem neoplasms
- MeSH C10.228.140.211.500.200 --- cerebellar neoplasms
- MeSH C10.228.140.211.692 --- neurocytoma
- MeSH C10.228.140.211.788 --- pinealoma
- MeSH C10.228.140.211.885 --- supratentorial neoplasms
- MeSH C10.228.140.211.885.500 --- hypothalamic neoplasms
- MeSH C10.228.140.211.885.500.600 --- pituitary neoplasms
- MeSH C10.228.140.252 --- cerebellar diseases
- MeSH C10.228.140.252.190 --- cerebellar ataxia
- MeSH C10.228.140.252.190.530 --- spinocerebellar ataxias
- MeSH C10.228.140.252.190.530.060 --- ataxia telangiectasia
- MeSH C10.228.140.252.190.530.530 --- machado-joseph disease
- MeSH C10.228.140.252.200 --- cerebellar neoplasms
- MeSH C10.228.140.252.300 --- dandy-walker syndrome
- MeSH C10.228.140.252.500 --- miller fisher syndrome
- MeSH C10.228.140.252.620 --- paraneoplastic cerebellar degeneration
- MeSH C10.228.140.252.700 --- spinocerebellar degenerations
- MeSH C10.228.140.252.700.150 --- friedreich ataxia
- MeSH C10.228.140.252.700.250 --- myoclonic cerebellar dyssynergia
- MeSH C10.228.140.252.700.650 --- olivopontocerebellar atrophies
- MeSH C10.228.140.252.700.700 --- spinocerebellar ataxias
- MeSH C10.228.140.252.700.700.500 --- machado-joseph disease
- MeSH C10.228.140.300 --- cerebrovascular disorders
- MeSH C10.228.140.300.100 --- basal ganglia cerebrovascular disease
- MeSH C10.228.140.300.100.200 --- basal ganglia hemorrhage
- MeSH C10.228.140.300.100.200.500 --- putaminal hemorrhage
- MeSH C10.228.140.300.150 --- brain ischemia
- MeSH C10.228.140.300.150.956 --- vertebrobasilar insufficiency
- MeSH C10.228.140.300.150.956.700 --- subclavian steal syndrome
- MeSH C10.228.140.300.200 --- carotid artery diseases
- MeSH C10.228.140.300.200.331 --- carotid artery thrombosis
- MeSH C10.228.140.300.200.345 --- carotid artery injuries
- MeSH C10.228.140.300.200.345.300 --- carotid artery, internal, dissection
- MeSH C10.228.140.300.200.345.350 --- carotid-cavernous sinus fistula
- MeSH C10.228.140.300.200.353 --- carotid artery, internal, dissection
- MeSH C10.228.140.300.200.360 --- carotid stenosis
- MeSH C10.228.140.300.200.490 --- carotid-cavernous sinus fistula
- MeSH C10.228.140.300.200.600 --- moyamoya disease
- MeSH C10.228.140.300.301 --- cerebrovascular accident
- MeSH C10.228.140.300.301.200 --- brain infarction
- MeSH C10.228.140.300.301.200.100 --- brain stem infarctions
- MeSH C10.228.140.300.301.200.100.500 --- lateral medullary syndrome
- MeSH C10.228.140.300.301.200.200 --- cerebral infarction
- MeSH C10.228.140.300.301.200.200.400 --- infarction, anterior cerebral artery
- MeSH C10.228.140.300.301.200.200.450 --- infarction, middle cerebral artery
- MeSH C10.228.140.300.301.200.200.475 --- infarction, posterior cerebral artery
- MeSH C10.228.140.300.350 --- cerebrovascular trauma
- MeSH C10.228.140.300.350.500 --- carotid artery injuries
- MeSH C10.228.140.300.350.500.300 --- carotid artery, internal, dissection
- MeSH C10.228.140.300.350.500.350 --- carotid-cavernous sinus fistula
- MeSH C10.228.140.300.350.875 --- vertebral artery dissection
- MeSH C10.228.140.300.400 --- dementia, vascular
- MeSH C10.228.140.300.400.203 --- cadasil
- MeSH C10.228.140.300.400.408 --- dementia, multi-infarct
- MeSH C10.228.140.300.451 --- hypoxia-ischemia, brain
- MeSH C10.228.140.300.451.200 --- brain ischemia
- MeSH C10.228.140.300.451.200.400 --- ischemic attack, transient
- MeSH C10.228.140.300.451.400 --- hypoxia, brain
- MeSH C10.228.140.300.510 --- intracranial arterial diseases
- MeSH C10.228.140.300.510.200 --- cerebral arterial diseases
- MeSH C10.228.140.300.510.200.175 --- cadasil
- MeSH C10.228.140.300.510.200.200 --- cerebral amyloid angiopathy
- MeSH C10.228.140.300.510.200.200.160 --- cerebral amyloid angiopathy, familial
- MeSH C10.228.140.300.510.200.325 --- infarction, anterior cerebral artery
- MeSH C10.228.140.300.510.200.387 --- infarction, middle cerebral artery
- MeSH C10.228.140.300.510.200.418 --- infarction, posterior cerebral artery
- MeSH C10.228.140.300.510.200.450 --- intracranial aneurysm
- MeSH C10.228.140.300.510.200.475 --- intracranial arteriosclerosis
- MeSH C10.228.140.300.510.200.475.500 --- dementia, vascular
- MeSH C10.228.140.300.510.400 --- intracranial arteriovenous malformations
- MeSH C10.228.140.300.520 --- intracranial arteriovenous malformations
- MeSH C10.228.140.300.525 --- intracranial embolism and thrombosis
- MeSH C10.228.140.300.525.400 --- intracranial embolism
- MeSH C10.228.140.300.525.425 --- intracranial thrombosis
- MeSH C10.228.140.300.525.669 --- sinus thrombosis, intracranial
- MeSH C10.228.140.300.525.669.375 --- cavernous sinus thrombosis
- MeSH C10.228.140.300.525.669.562 --- lateral sinus thrombosis
- MeSH C10.228.140.300.525.669.750 --- sagittal sinus thrombosis
- MeSH C10.228.140.300.535 --- intracranial hemorrhages
- MeSH C10.228.140.300.535.200 --- cerebral hemorrhage
- MeSH C10.228.140.300.535.200.150 --- basal ganglia hemorrhage
- MeSH C10.228.140.300.535.200.150.500 --- putaminal hemorrhage
- MeSH C10.228.140.300.535.200.200 --- cerebral hemorrhage, traumatic
- MeSH C10.228.140.300.535.325 --- intracranial hemorrhage, hypertensive
- MeSH C10.228.140.300.535.450 --- intracranial hemorrhage, traumatic
- MeSH C10.228.140.300.535.450.200 --- brain hemorrhage, traumatic
- MeSH C10.228.140.300.535.450.200.500 --- brain stem hemorrhage, traumatic
- MeSH C10.228.140.300.535.450.200.750 --- cerebral hemorrhage, traumatic
- MeSH C10.228.140.300.535.450.300 --- hematoma, epidural, cranial
- MeSH C10.228.140.300.535.450.400 --- hematoma, subdural
- MeSH C10.228.140.300.535.450.400.050 --- hematoma, subdural, acute
- MeSH C10.228.140.300.535.450.400.120 --- hematoma, subdural, chronic
- MeSH C10.228.140.300.535.450.400.400 --- hematoma, subdural, intracranial
- MeSH C10.228.140.300.535.450.650 --- subarachnoid hemorrhage, traumatic
- MeSH C10.228.140.300.535.625 --- pituitary apoplexy
- MeSH C10.228.140.300.535.800 --- subarachnoid hemorrhage
- MeSH C10.228.140.300.535.800.700 --- subarachnoid hemorrhage, traumatic
- MeSH C10.228.140.300.700 --- leukomalacia, periventricular
- MeSH C10.228.140.300.750 --- sneddon syndrome
- MeSH C10.228.140.300.800 --- vascular headaches
- MeSH C10.228.140.300.850 --- vasculitis, central nervous system
- MeSH C10.228.140.300.850.125 --- aids arteritis, central nervous system
- MeSH C10.228.140.300.850.250 --- lupus vasculitis, central nervous system
- MeSH C10.228.140.300.850.500 --- temporal arteritis
- MeSH C10.228.140.300.900 --- vasospasm, intracranial
- MeSH C10.228.140.300.950 --- vertebral artery dissection
- MeSH C10.228.140.380 --- dementia
- MeSH C10.228.140.380.070 --- aids dementia complex
- MeSH C10.228.140.380.100 --- alzheimer disease
- MeSH C10.228.140.380.132 --- aphasia, primary progressive
- MeSH C10.228.140.380.165 --- creutzfeldt-jakob syndrome
- MeSH C10.228.140.380.230 --- dementia, vascular
- MeSH C10.228.140.380.230.250 --- dementia, multi-infarct
- MeSH C10.228.140.380.278 --- huntington disease
- MeSH C10.228.140.380.326 --- Klüver-Bucy syndrome
- MeSH C10.228.140.380.422 --- lewy body disease
- MeSH C10.228.140.380.615 --- pick disease of the brain
- MeSH C10.228.140.400 --- diffuse cerebral sclerosis of schilder
- MeSH C10.228.140.430 --- encephalitis
- MeSH C10.228.140.430.500 --- encephalomyelitis
- MeSH C10.228.140.430.525 --- limbic encephalitis
- MeSH C10.228.140.430.550 --- meningoencephalitis
- MeSH C10.228.140.430.550.500 --- lupus vasculitis, central nervous system
- MeSH C10.228.140.461 --- encephalomalacia
- MeSH C10.228.140.461.550 --- leukomalacia, periventricular
- MeSH C10.228.140.490 --- epilepsy
- MeSH C10.228.140.490.250 --- epilepsies, myoclonic
- MeSH C10.228.140.490.250.300 --- myoclonic epilepsy, juvenile
- MeSH C10.228.140.490.250.650 --- myoclonic epilepsies, progressive
- MeSH C10.228.140.490.250.650.500 --- lafora disease
- MeSH C10.228.140.490.250.650.700 --- merrf syndrome
- MeSH C10.228.140.490.250.650.900 --- unverricht-lundborg syndrome
- MeSH C10.228.140.490.360 --- epilepsies, partial
- MeSH C10.228.140.490.360.260 --- epilepsy, complex partial
- MeSH C10.228.140.490.360.270 --- epilepsy, frontal lobe
- MeSH C10.228.140.490.360.272 --- epilepsy, partial, motor
- MeSH C10.228.140.490.360.275 --- epilepsy, partial, sensory
- MeSH C10.228.140.490.360.280 --- epilepsy, rolandic
- MeSH C10.228.140.490.360.290 --- epilepsy, temporal lobe
- MeSH C10.228.140.490.370 --- epilepsy, benign neonatal
- MeSH C10.228.140.490.375 --- epilepsy, generalized
- MeSH C10.228.140.490.375.260 --- epilepsy, absence
- MeSH C10.228.140.490.375.290 --- epilepsy, tonic-clonic
- MeSH C10.228.140.490.375.760 --- spasms, infantile
- MeSH C10.228.140.490.380 --- epilepsy, post-traumatic
- MeSH C10.228.140.490.450 --- epilepsy, reflex
- MeSH C10.228.140.490.535 --- landau-kleffner syndrome
- MeSH C10.228.140.490.631 --- seizures
- MeSH C10.228.140.490.650 --- seizures, febrile
- MeSH C10.228.140.490.690 --- status epilepticus
- MeSH C10.228.140.490.690.260 --- epilepsia partialis continua
- MeSH C10.228.140.546 --- headache disorders
- MeSH C10.228.140.546.399 --- headache disorders, primary
- MeSH C10.228.140.546.399.750 --- migraine disorders
- MeSH C10.228.140.546.399.750.250 --- migraine with aura
- MeSH C10.228.140.546.399.750.450 --- migraine without aura
- MeSH C10.228.140.546.399.875 --- tension-type headache
- MeSH C10.228.140.546.399.937 --- trigeminal autonomic cephalalgias
- MeSH C10.228.140.546.399.937.500 --- cluster headache
- MeSH C10.228.140.546.399.937.750 --- paroxysmal hemicrania
- MeSH C10.228.140.546.399.937.875 --- sunct syndrome
- MeSH C10.228.140.546.699 --- headache disorders, secondary
- MeSH C10.228.140.546.699.124 --- post-dural puncture headache
- MeSH C10.228.140.546.699.249 --- post-traumatic headache
- MeSH C10.228.140.546.699.500 --- vascular headaches
- MeSH C10.228.140.602 --- hydrocephalus
- MeSH C10.228.140.602.288 --- dandy-walker syndrome
- MeSH C10.228.140.602.559 --- hydrocephalus, normal pressure
- MeSH C10.228.140.617 --- hypothalamic diseases
- MeSH C10.228.140.617.200 --- bardet-biedl syndrome
- MeSH C10.228.140.617.477 --- hypothalamic neoplasms
- MeSH C10.228.140.617.477.600 --- pituitary neoplasms
- MeSH C10.228.140.617.500 --- laurence-moon syndrome
- MeSH C10.228.140.617.738 --- pituitary diseases
- MeSH C10.228.140.617.738.200 --- empty sella syndrome
- MeSH C10.228.140.617.738.250 --- hyperpituitarism
- MeSH C10.228.140.617.738.250.100 --- acromegaly
- MeSH C10.228.140.617.738.250.450 --- hyperprolactinemia
- MeSH C10.228.140.617.738.250.725 --- pituitary acth hypersecretion
- MeSH C10.228.140.617.738.300 --- hypopituitarism
- MeSH C10.228.140.617.738.300.300 --- dwarfism, pituitary
- MeSH C10.228.140.617.738.320 --- inappropriate adh syndrome
- MeSH C10.228.140.617.738.350 --- pituitary apoplexy
- MeSH C10.228.140.617.738.675 --- pituitary neoplasms
- MeSH C10.228.140.617.738.675.149 --- acth-secreting pituitary adenoma
- MeSH C10.228.140.617.738.675.149.500 --- nelson syndrome
- MeSH C10.228.140.617.738.675.299 --- growth hormone-secreting pituitary adenoma
- MeSH C10.228.140.617.738.675.800 --- prolactinoma
- MeSH C10.228.140.631 --- intracranial hypertension
- MeSH C10.228.140.631.450 --- hydrocephalus
- MeSH C10.228.140.631.450.500 --- dandy-walker syndrome
- MeSH C10.228.140.631.500 --- hypertensive encephalopathy
- MeSH C10.228.140.631.750 --- pseudotumor cerebri
- MeSH C10.228.140.638 --- intracranial hypotension
- MeSH C10.228.140.646 --- kluver-Bucy syndrome
- MeSH C10.228.140.744 --- neuroaxonal dystrophies
- MeSH C10.228.140.744.320 --- hallervorden-spatz syndrome
- MeSH C10.228.140.870 --- subdural effusion
- MeSH C10.228.140.915 --- thalamic diseases
MeSH C10.228.228 --- central nervous system infections[sửa]
- MeSH C10.228.228.090 --- brain abscess
- MeSH C10.228.228.090.800 --- toxoplasmosis, cerebral
- MeSH C10.228.228.180 --- central nervous system bacterial infections
- MeSH C10.228.228.180.100 --- brain abscess
- MeSH C10.228.228.180.350 --- empyema, subdural
- MeSH C10.228.228.180.375 --- epidural abscess
- MeSH C10.228.228.180.437 --- lyme neuroborreliosis
- MeSH C10.228.228.180.500 --- meningitis, bacterial
- MeSH C10.228.228.180.500.350 --- meningitis, escherichia coli
- MeSH C10.228.228.180.500.425 --- meningitis, haemophilus
- MeSH C10.228.228.180.500.500 --- meningitis, listeria
- MeSH C10.228.228.180.500.750 --- meningitis, meningococcal
- MeSH C10.228.228.180.500.750.500 --- waterhouse-friderichsen syndrome
- MeSH C10.228.228.180.500.875 --- meningitis, pneumococcal
- MeSH C10.228.228.180.500.937 --- tuberculosis, meningeal
- MeSH C10.228.228.180.600 --- neurosyphilis
- MeSH C10.228.228.180.600.800 --- tabes dorsalis
- MeSH C10.228.228.180.850 --- tuberculosis, central nervous system
- MeSH C10.228.228.180.850.400 --- tuberculoma, intracranial
- MeSH C10.228.228.180.850.800 --- tuberculosis, meningeal
- MeSH C10.228.228.198 --- central nervous system fungal infections
- MeSH C10.228.228.198.500 --- meningitis, fungal
- MeSH C10.228.228.198.500.500 --- meningitis, cryptococcal
- MeSH C10.228.228.198.750 --- neuroaspergillosis
- MeSH C10.228.228.205 --- central nervous system parasitic infections
- MeSH C10.228.228.205.250 --- central nervous system helminthiasis
- MeSH C10.228.228.205.250.550 --- neurocysticercosis
- MeSH C10.228.228.205.250.600 --- neuroschistosomiasis
- MeSH C10.228.228.205.300 --- central nervous system protozoal infections
- MeSH C10.228.228.205.300.500 --- malaria, cerebral
- MeSH C10.228.228.205.300.800 --- toxoplasmosis, cerebral
- MeSH C10.228.228.205.300.900 --- toxoplasmosis, congenital
- MeSH C10.228.228.210 --- central nervous system viral diseases
- MeSH C10.228.228.210.150 --- encephalitis
- MeSH C10.228.228.210.150.300 --- encephalitis, viral
- MeSH C10.228.228.210.150.300.300 --- encephalitis, arbovirus
- MeSH C10.228.228.210.150.300.300.200 --- encephalitis, california
- MeSH C10.228.228.210.150.300.300.400 --- encephalitis, japanese
- MeSH C10.228.228.210.150.300.300.550 --- encephalitis, st. louis
- MeSH C10.228.228.210.150.300.300.775 --- encephalitis, tick-borne
- MeSH C10.228.228.210.150.300.300.887 --- west nile fever
- MeSH C10.228.228.210.150.300.350 --- encephalitis, herpes simplex
- MeSH C10.228.228.210.150.300.400 --- encephalitis, varicella zoster
- MeSH C10.228.228.210.150.300.450 --- encephalomyelitis, equine
- MeSH C10.228.228.210.150.300.450.200 --- encephalomyelitis, eastern equine
- MeSH C10.228.228.210.150.300.450.600 --- encephalomyelitis, venezuelan equine
- MeSH C10.228.228.210.150.300.450.800 --- encephalomyelitis, western equine
- MeSH C10.228.228.210.150.300.500 --- leukoencephalopathy, progressive multifocal
- MeSH C10.228.228.210.150.300.600 --- subacute sclerosing panencephalitis
- MeSH C10.228.228.210.500 --- meningitis, viral
- MeSH C10.228.228.210.500.500 --- lymphocytic choriomeningitis
- MeSH C10.228.228.210.500.600 --- meningitis, aseptic
- MeSH C10.228.228.210.575 --- myelitis
- MeSH C10.228.228.210.575.500 --- paraparesis, tropical spastic
- MeSH C10.228.228.210.575.750 --- poliomyelitis
- MeSH C10.228.228.210.650 --- poliomyelitis
- MeSH C10.228.228.210.650.600 --- poliomyelitis, bulbar
- MeSH C10.228.228.210.650.800 --- postpoliomyelitis syndrome
- MeSH C10.228.228.210.710 --- pseudorabies
- MeSH C10.228.228.227 --- empyema, subdural
- MeSH C10.228.228.245 --- encephalitis
- MeSH C10.228.228.245.340 --- encephalitis, viral
- MeSH C10.228.228.245.340.310 --- encephalitis, arbovirus
- MeSH C10.228.228.245.340.310.140 --- encephalitis, california
- MeSH C10.228.228.245.340.310.280 --- encephalitis, japanese
- MeSH C10.228.228.245.340.310.406 --- encephalitis, st. louis
- MeSH C10.228.228.245.340.310.500 --- encephalitis, tick-borne
- MeSH C10.228.228.245.340.310.950 --- west nile fever
- MeSH C10.228.228.245.340.332 --- encephalitis, herpes simplex
- MeSH C10.228.228.245.340.355 --- encephalitis, varicella zoster
- MeSH C10.228.228.245.340.450 --- encephalomyelitis, equine
- MeSH C10.228.228.245.340.450.200 --- encephalomyelitis, eastern equine
- MeSH C10.228.228.245.340.450.225 --- encephalomyelitis, venezuelan equine
- MeSH C10.228.228.245.340.450.250 --- encephalomyelitis, western equine
- MeSH C10.228.228.245.340.575 --- leukoencephalopathy, progressive multifocal
- MeSH C10.228.228.245.340.700 --- subacute sclerosing panencephalitis
- MeSH C10.228.228.245.550 --- meningoencephalitis
- MeSH C10.228.228.245.550.500 --- lupus vasculitis, central nervous system
- MeSH C10.228.228.245.670 --- leukoencephalitis, acute hemorrhagic
- MeSH C10.228.228.245.700 --- limbic encephalitis
- MeSH C10.228.228.291 --- encephalomyelitis
- MeSH C10.228.228.291.323 --- encephalomyelitis, equine
- MeSH C10.228.228.291.323.162 --- encephalomyelitis, eastern equine
- MeSH C10.228.228.291.323.325 --- encephalomyelitis, venezuelan equine
- MeSH C10.228.228.291.323.662 --- encephalomyelitis, western equine
- MeSH C10.228.228.300 --- epidural abscess
- MeSH C10.228.228.507 --- meningitis
- MeSH C10.228.228.507.097 --- arachnoiditis
- MeSH C10.228.228.507.220 --- meningitis, aseptic
- MeSH C10.228.228.507.280 --- meningitis, bacterial
- MeSH C10.228.228.507.280.350 --- meningitis, escherichia coli
- MeSH C10.228.228.507.280.393 --- meningitis, haemophilus
- MeSH C10.228.228.507.280.449 --- meningitis, listeria
- MeSH C10.228.228.507.280.505 --- meningitis, meningococcal
- MeSH C10.228.228.507.280.505.904 --- waterhouse-friderichsen syndrome
- MeSH C10.228.228.507.280.560 --- meningitis, pneumococcal
- MeSH C10.228.228.507.280.915 --- tuberculosis, meningeal
- MeSH C10.228.228.507.400 --- meningitis, fungal
- MeSH C10.228.228.507.400.500 --- meningitis, cryptococcal
- MeSH C10.228.228.507.700 --- meningitis, viral
- MeSH C10.228.228.507.700.500 --- lymphocytic choriomeningitis
- MeSH C10.228.228.507.700.600 --- meningitis, aseptic
- MeSH C10.228.228.507.850 --- meningoencephalitis
- MeSH C10.228.228.507.850.500 --- lupus vasculitis, central nervous system
- MeSH C10.228.228.553 --- meningoencephalitis
- MeSH C10.228.228.553.450 --- lupus vasculitis, central nervous system
- MeSH C10.228.228.553.900 --- uveomeningoencephalitic syndrome
- MeSH C10.228.228.618 --- myelitis
- MeSH C10.228.228.618.700 --- paraparesis, tropical spastic
- MeSH C10.228.228.618.850 --- poliomyelitis
- MeSH C10.228.228.709 --- perimeningeal infections
- MeSH C10.228.228.709.300 --- empyema, subdural
- MeSH C10.228.228.709.350 --- epidural abscess
- MeSH C10.228.228.709.675 --- subdural effusion
- MeSH C10.228.228.800 --- prion diseases
- MeSH C10.228.228.800.230 --- creutzfeldt-jakob syndrome
- MeSH C10.228.228.800.260 --- encephalopathy, bovine spongiform
- MeSH C10.228.228.800.350 --- gerstmann-straussler-scheinker disease
- MeSH C10.228.228.800.392 --- insomnia, fatal familial
- MeSH C10.228.228.800.435 --- kuru
- MeSH C10.228.228.800.717 --- scrapie
- MeSH C10.228.228.800.858 --- wasting disease, chronic
MeSH C10.228.440 --- encephalomyelitis[sửa]
- MeSH C10.228.440.406 --- encephalomyelitis, equine
- MeSH C10.228.440.406.200 --- encephalomyelitis, eastern equine
- MeSH C10.228.440.406.225 --- encephalomyelitis, venezuelan equine
- MeSH C10.228.440.406.250 --- encephalomyelitis, western equine
- MeSH C10.228.440.600 --- fatigue syndrome, chronic
- MeSH C10.228.440.650 --- leukoencephalitis, acute hemorrhagic
MeSH C10.228.470 --- high pressure neurological syndrome[sửa]
MeSH C10.228.566 --- meningitis[sửa]
- MeSH C10.228.566.500 --- meningoencephalitis
- MeSH C10.228.566.500.500 --- lupus vasculitis, central nervous system
MeSH C10.228.662 --- movement disorders[sửa]
- MeSH C10.228.662.075 --- angelman syndrome
- MeSH C10.228.662.150 --- choreatic disorders
- MeSH C10.228.662.150.500 --- chorea gravidarum
- MeSH C10.228.662.150.550 --- huntington disease
- MeSH C10.228.662.300 --- dystonic disorders
- MeSH C10.228.662.300.200 --- dystonia musculorum deformans
- MeSH C10.228.662.300.500 --- meige syndrome
- MeSH C10.228.662.300.750 --- torticollis
- MeSH C10.228.662.350 --- essential tremor
- MeSH C10.228.662.400 --- hallervorden-spatz syndrome
- MeSH C10.228.662.425 --- hepatolenticular degeneration
- MeSH C10.228.662.550 --- multiple system atrophy
- MeSH C10.228.662.550.600 --- olivopontocerebellar atrophies
- MeSH C10.228.662.550.700 --- shy-drager syndrome
- MeSH C10.228.662.550.800 --- striatonigral degeneration
- MeSH C10.228.662.600 --- parkinsonian disorders
- MeSH C10.228.662.600.200 --- lewy body disease
- MeSH C10.228.662.600.400 --- parkinson disease
- MeSH C10.228.662.600.700 --- parkinson disease, secondary
- MeSH C10.228.662.600.700.250 --- mptp poisoning
- MeSH C10.228.662.600.700.500 --- parkinson disease, postencephalitic
- MeSH C10.228.662.700 --- supranuclear palsy, progressive
- MeSH C10.228.662.825 --- Tic disorders
- MeSH C10.228.662.825.800 --- Tourette syndrome
MeSH C10.228.758 --- ocular motility disorders[sửa]
MeSH C10.228.806 --- pneumocephalus[sửa]
MeSH C10.228.854 --- spinal cord diseases[sửa]
- MeSH C10.228.854.139 --- amyotrophic lateral sclerosis
- MeSH C10.228.854.303 --- epidural abscess
- MeSH C10.228.854.468 --- muscular atrophy, spinal
- MeSH C10.228.854.468.800 --- spinal muscular atrophies of childhood
- MeSH C10.228.854.525 --- myelitis
- MeSH C10.228.854.525.553 --- myelitis, transverse
- MeSH C10.228.854.525.700 --- paraparesis, tropical spastic
- MeSH C10.228.854.525.850 --- poliomyelitis
- MeSH C10.228.854.641 --- poliomyelitis
- MeSH C10.228.854.641.650 --- postpoliomyelitis syndrome
- MeSH C10.228.854.761 --- spinal cord compression
- MeSH C10.228.854.765 --- spinal cord neoplasms
- MeSH C10.228.854.765.342 --- epidural neoplasms
- MeSH C10.228.854.770 --- spinal cord injuries
- MeSH C10.228.854.770.500 --- central cord syndrome
- MeSH C10.228.854.785 --- spinal cord vascular diseases
- MeSH C10.228.854.785.100 --- anterior spinal artery syndrome
- MeSH C10.228.854.785.650 --- spinal cord ischemia
- MeSH C10.228.854.785.650.100 --- anterior spinal artery syndrome
- MeSH C10.228.854.787 --- spinocerebellar degenerations
- MeSH C10.228.854.787.200 --- friedreich ataxia
- MeSH C10.228.854.787.500 --- myoclonic cerebellar dyssynergia
- MeSH C10.228.854.787.750 --- olivopontocerebellar atrophies
- MeSH C10.228.854.787.875 --- spinocerebellar ataxias
- MeSH C10.228.854.787.875.500 --- machado-joseph disease
- MeSH C10.228.854.790 --- stiff-person syndrome
- MeSH C10.228.854.833 --- syringomyelia
- MeSH C10.228.854.889 --- tabes dorsalis
MeSH C10.281 --- chronobiology disorders[sửa]
MeSH C10.281.440 --- jet lag syndrome[sửa]
MeSH C10.281.800 --- sleep disorders, circadian rhythm[sửa]
MeSH C10.292 --- cranial nerve diseases[sửa]
MeSH C10.292.150 --- abducens nerve diseases[sửa]
MeSH C10.292.175 --- accessory nerve diseases[sửa]
MeSH C10.292.225 --- cranial nerve neoplasms[sửa]
- MeSH C10.292.225.750 --- neuroma, acoustic
- MeSH C10.292.225.750.500 --- neurofibromatosis 2
- MeSH C10.292.225.800 --- optic nerve neoplasms
- MeSH C10.292.225.800.500 --- optic nerve glioma
MeSH C10.292.262 --- cranial nerve injuries[sửa]
- MeSH C10.292.262.200 --- abducens nerve injury
- MeSH C10.292.262.500 --- facial nerve injuries
- MeSH C10.292.262.750 --- optic nerve injuries
MeSH C10.292.300 --- facial nerve diseases[sửa]
- MeSH C10.292.300.250 --- bell palsy
- MeSH C10.292.300.375 --- facial hemiatrophy
- MeSH C10.292.300.500 --- facial nerve injuries
- MeSH C10.292.300.625 --- facial neuralgia
- MeSH C10.292.300.750 --- herpes zoster oticus
- MeSH C10.292.300.800 --- melkersson-rosenthal syndrome
- MeSH C10.292.300.825 --- mobius syndrome
MeSH C10.292.375 --- facial neuralgia[sửa]
MeSH C10.292.450 --- glossopharyngeal nerve diseases[sửa]
MeSH C10.292.525 --- hypoglossal nerve diseases[sửa]
MeSH C10.292.562 --- ocular motility disorders[sửa]
- MeSH C10.292.562.250 --- duane retraction syndrome
- MeSH C10.292.562.350 --- miller fisher syndrome
- MeSH C10.292.562.675 --- nystagmus, pathologic
- MeSH C10.292.562.675.300 --- nystagmus, congenital
- MeSH C10.292.562.700 --- oculomotor nerve diseases
- MeSH C10.292.562.750 --- ophthalmoplegia
- MeSH C10.292.562.750.250 --- ophthalmoplegia, chronic progressive external
- MeSH C10.292.562.750.500 --- supranuclear palsy, progressive
- MeSH C10.292.562.775 --- ophthalmoplegia, chronic progressive external
- MeSH C10.292.562.775.500 --- kearns-sayer syndrome
- MeSH C10.292.562.887 --- strabismus
- MeSH C10.292.562.887.300 --- esotropia
- MeSH C10.292.562.887.650 --- exotropia
- MeSH C10.292.562.900 --- tolosa-hunt syndrome
MeSH C10.292.600 --- oculomotor nerve diseases[sửa]
MeSH C10.292.650 --- olfactory nerve diseases[sửa]
MeSH C10.292.700 --- optic nerve diseases[sửa]
- MeSH C10.292.700.225 --- optic atrophy
- MeSH C10.292.700.225.500 --- optic atrophies, hereditary
- MeSH C10.292.700.225.500.400 --- optic atrophy, hereditary, leber
- MeSH C10.292.700.225.500.500 --- optic atrophy, autosomal dominant
- MeSH C10.292.700.225.500.980 --- wolfram syndrome
- MeSH C10.292.700.450 --- optic disk drusen
- MeSH C10.292.700.475 --- optic nerve injuries
- MeSH C10.292.700.500 --- optic nerve neoplasms
- MeSH C10.292.700.500.500 --- optic nerve glioma
- MeSH C10.292.700.550 --- optic neuritis
- MeSH C10.292.700.550.500 --- neuromyelitis optica
- MeSH C10.292.700.600 --- optic neuropathy, ischemic
- MeSH C10.292.700.900 --- papilledema
MeSH C10.292.775 --- trigeminal nerve diseases[sửa]
MeSH C10.292.850 --- trochlear nerve diseases[sửa]
MeSH C10.292.887 --- vagus nerve diseases[sửa]
MeSH C10.292.910 --- vestibulocochlear nerve diseases[sửa]
- MeSH C10.292.910.600 --- neuroma, acoustic
- MeSH C10.292.910.600.500 --- neurofibromatosis 2
- MeSH C10.292.910.850 --- vestibular neuronitis
MeSH C10.314 --- demyelinating diseases[sửa]
MeSH C10.314.350 --- demyelinating autoimmune diseases, cns[sửa]
- MeSH C10.314.350.112 --- diffuse cerebral sclerosis of schilder
- MeSH C10.314.350.225 --- encephalomyelitis, acute disseminated
- MeSH C10.314.350.250 --- encephalomyelitis, autoimmune, experimental
- MeSH C10.314.350.375 --- leukoencephalitis, acute hemorrhagic
- MeSH C10.314.350.500 --- multiple sclerosis
- MeSH C10.314.350.500.200 --- multiple sclerosis, chronic progressive
- MeSH C10.314.350.500.600 --- multiple sclerosis, relapsing-remitting
- MeSH C10.314.350.500.650 --- neuromyelitis optica
- MeSH C10.314.350.600 --- myelitis, transverse
- MeSH C10.314.350.600.500 --- neuromyelitis optica
- MeSH C10.314.350.650 --- neuromyelitis optica
MeSH C10.314.400 --- hereditary central nervous system demyelinating diseases[sửa]
- MeSH C10.314.400.250 --- adrenoleukodystrophy
- MeSH C10.314.400.312 --- alexander disease
- MeSH C10.314.400.375 --- canavan disease
- MeSH C10.314.400.500 --- leukodystrophy, globoid cell
- MeSH C10.314.400.550 --- leukodystrophy, metachromatic
- MeSH C10.314.400.775 --- pelizaeus-merzbacher disease
MeSH C10.314.450 --- leukoencephalopathy, progressive multifocal[sửa]
MeSH C10.314.500 --- myelinolysis, central pontine[sửa]
MeSH C10.314.750 --- polyradiculoneuropathy[sửa]
- MeSH C10.314.750.300 --- polyradiculoneuropathy, chronic inflammatory demyelinating
- MeSH C10.314.750.450 --- guillain-barre syndrome
- MeSH C10.314.750.450.500 --- miller fisher syndrome
- MeSH C10.314.750.600 --- hereditary sensory and autonomic neuropathies
- MeSH C10.314.750.600.250 --- dysautonomia, familial
MeSH C10.500 --- nervous system malformations[sửa]
MeSH C10.500.142 --- central nervous system cysts[sửa]
MeSH C10.500.190 --- central nervous system vascular malformations[sửa]
- MeSH C10.500.190.200 --- hemangioma, cavernous, central nervous system
- MeSH C10.500.190.600 --- central nervous system venous angioma
- MeSH C10.500.190.800 --- sinus pericranii
MeSH C10.500.205 --- dandy-walker syndrome[sửa]
MeSH C10.500.300 --- hereditary motor and sensory neuropathies[sửa]
- MeSH C10.500.300.200 --- charcot-marie-tooth disease
- MeSH C10.500.300.780 --- refsum disease
- MeSH C10.500.300.820 --- spastic paraplegia, hereditary
MeSH C10.500.310 --- hereditary sensory and autonomic neuropathies[sửa]
MeSH C10.500.410 --- holoprosencephaly[sửa]
MeSH C10.500.450 --- hydranencephaly[sửa]
MeSH C10.500.460 --- intracranial arteriovenous malformations[sửa]
MeSH C10.500.680 --- neural tube defects[sửa]
- MeSH C10.500.680.196 --- anencephaly
- MeSH C10.500.680.291 --- arnold-chiari malformation
- MeSH C10.500.680.488 --- encephalocele
- MeSH C10.500.680.598 --- meningocele
- MeSH C10.500.680.610 --- meningomyelocele
- MeSH C10.500.680.800 --- spinal dysraphism
- MeSH C10.500.680.800.730 --- spina bifida cystica
- MeSH C10.500.680.800.750 --- spina bifida occulta
MeSH C10.500.840 --- septo-optic dysplasia[sửa]
MeSH C10.551 --- nervous system neoplasms[sửa]
MeSH C10.551.240 --- central nervous system neoplasms[sửa]
- MeSH C10.551.240.250 --- brain neoplasms
- MeSH C10.551.240.250.200 --- cerebral ventricle neoplasms
- MeSH C10.551.240.250.200.200 --- choroid plexus neoplasms
- MeSH C10.551.240.250.200.200.500 --- papilloma, choroid plexus
- MeSH C10.551.240.250.400 --- infratentorial neoplasms
- MeSH C10.551.240.250.400.200 --- brain stem neoplasms
- MeSH C10.551.240.250.400.300 --- cerebellar neoplasms
- MeSH C10.551.240.250.550 --- neurocytoma
- MeSH C10.551.240.250.625 --- pinealoma
- MeSH C10.551.240.250.700 --- supratentorial neoplasms
- MeSH C10.551.240.250.700.500 --- hypothalamic neoplasms
- MeSH C10.551.240.250.700.500.500 --- pituitary neoplasms
- MeSH C10.551.240.375 --- central nervous system cysts
- MeSH C10.551.240.375.500 --- arachnoid cysts
- MeSH C10.551.240.500 --- meningeal neoplasms
- MeSH C10.551.240.500.500 --- meningioma
- MeSH C10.551.240.750 --- spinal cord neoplasms
- MeSH C10.551.240.750.200 --- epidural neoplasms
MeSH C10.551.360 --- cranial nerve neoplasms[sửa]
MeSH C10.551.525 --- neuroma, acoustic[sửa]
MeSH C10.551.775 --- peripheral nervous system neoplasms[sửa]
- MeSH C10.551.775.500 --- nerve sheath neoplasms
- MeSH C10.551.775.500.500 --- neurilemmoma
- MeSH C10.551.775.500.750 --- neurofibroma
- MeSH C10.551.775.500.750.500 --- neurofibroma, plexiform
- MeSH C10.551.775.500.750.750 --- neurofibrosarcoma
MeSH C10.562 --- neurocutaneous syndromes[sửa]
MeSH C10.562.100 --- ataxia telangiectasia[sửa]
MeSH C10.562.400 --- hippel-lindau disease[sửa]
MeSH C10.562.600 --- neurofibromatosis[sửa]
MeSH C10.562.800 --- sturge-weber syndrome[sửa]
MeSH C10.562.850 --- tuberous sclerosis[sửa]
MeSH C10.574 --- neurodegenerative diseases[sửa]
MeSH C10.574.500 --- heredodegenerative disorders, nervous system[sửa]
- MeSH C10.574.500.024 --- alexander disease
- MeSH C10.574.500.050 --- amyloid neuropathies, familial
- MeSH C10.574.500.300 --- canavan disease
- MeSH C10.574.500.362 --- cockayne syndrome
- MeSH C10.574.500.393 --- dystonia musculorum deformans
- MeSH C10.574.500.425 --- gerstmann-straussler-scheinker disease
- MeSH C10.574.500.487 --- hallervorden-spatz syndrome
- MeSH C10.574.500.492 --- hepatolenticular degeneration
- MeSH C10.574.500.494 --- hereditary central nervous system demyelinating diseases
- MeSH C10.574.500.495 --- hereditary motor and sensory neuropathies
- MeSH C10.574.500.495.200 --- charcot-marie-tooth disease
- MeSH C10.574.500.495.780 --- refsum disease
- MeSH C10.574.500.495.820 --- spastic paraplegia, hereditary
- MeSH C10.574.500.496 --- hereditary sensory and autonomic neuropathies
- MeSH C10.574.500.496.250 --- dysautonomia, familial
- MeSH C10.574.500.497 --- huntington disease
- MeSH C10.574.500.529 --- lafora disease
- MeSH C10.574.500.536 --- lesch-nyhan syndrome
- MeSH C10.574.500.540 --- menkes kinky hair syndrome
- MeSH C10.574.500.545 --- myotonia congenita
- MeSH C10.574.500.547 --- myotonic dystrophy
- MeSH C10.574.500.549 --- neurofibromatosis
- MeSH C10.574.500.549.400 --- neurofibromatosis 1
- MeSH C10.574.500.549.700 --- neurofibromatosis 2
- MeSH C10.574.500.550 --- neuronal ceroid-lipofuscinosis
- MeSH C10.574.500.662 --- optic atrophies, hereditary
- MeSH C10.574.500.662.400 --- optic atrophy, hereditary, leber
- MeSH C10.574.500.662.500 --- optic atrophy, autosomal dominant
- MeSH C10.574.500.662.980 --- wolfram syndrome
- MeSH C10.574.500.775 --- rett syndrome
- MeSH C10.574.500.812 --- spinal muscular atrophies of childhood
- MeSH C10.574.500.825 --- spinocerebellar degenerations
- MeSH C10.574.500.825.200 --- friedreich ataxia
- MeSH C10.574.500.825.250 --- myoclonic cerebellar dyssynergia
- MeSH C10.574.500.825.650 --- olivopontocerebellar atrophies
- MeSH C10.574.500.825.700 --- spinocerebellar ataxias
- MeSH C10.574.500.825.700.500 --- machado-joseph disease
- MeSH C10.574.500.850 --- tourette syndrome
- MeSH C10.574.500.865 --- tuberous sclerosis
- MeSH C10.574.500.875 --- unverricht-lundborg syndrome
MeSH C10.574.531 --- lewy body disease[sửa]
MeSH C10.574.562 --- motor neuron disease[sửa]
- MeSH C10.574.562.250 --- amyotrophic lateral sclerosis
- MeSH C10.574.562.300 --- bulbar palsy, progressive
- MeSH C10.574.562.500 --- muscular atrophy, spinal
- MeSH C10.574.562.500.750 --- spinal muscular atrophies of childhood
MeSH C10.574.625 --- multiple system atrophy[sửa]
- MeSH C10.574.625.600 --- olivopontocerebellar atrophies
- MeSH C10.574.625.700 --- shy-drager syndrome
- MeSH C10.574.625.800 --- striatonigral degeneration
MeSH C10.574.750 --- olivopontocerebellar atrophies[sửa]
MeSH C10.574.781 --- paraneoplastic syndromes, nervous system[sửa]
- MeSH C10.574.781.500 --- lambert-eaton myasthenic syndrome
- MeSH C10.574.781.550 --- limbic encephalitis
- MeSH C10.574.781.625 --- myelitis, transverse
- MeSH C10.574.781.700 --- paraneoplastic cerebellar degeneration
- MeSH C10.574.781.850 --- paraneoplastic polyneuropathy
MeSH C10.574.812 --- parkinson disease[sửa]
MeSH C10.574.827 --- postpoliomyelitis syndrome[sửa]
MeSH C10.574.843 --- prion diseases[sửa]
- MeSH C10.574.843.300 --- encephalopathy, bovine spongiform
- MeSH C10.574.843.400 --- gerstmann-straussler-scheinker disease
- MeSH C10.574.843.512 --- insomnia, fatal familial
- MeSH C10.574.843.625 --- kuru
- MeSH C10.574.843.850 --- scrapie
- MeSH C10.574.843.925 --- wasting disease, chronic
MeSH C10.574.875 --- shy-drager syndrome[sửa]
MeSH C10.574.945 --- tauopathies[sửa]
MeSH C10.597 --- neurologic manifestations[sửa]
MeSH C10.597.200 --- bladder, neurogenic[sửa]
MeSH C10.597.230 --- cerebrospinal fluid otorrhea[sửa]
MeSH C10.597.267 --- cerebrospinal fluid rhinorrhea[sửa]
MeSH C10.597.305 --- decerebrate state[sửa]
MeSH C10.597.350 --- dyskinesias[sửa]
- MeSH C10.597.350.090 --- ataxia
- MeSH C10.597.350.090.500 --- cerebellar ataxia
- MeSH C10.597.350.090.500.530 --- spinocerebellar ataxias
- MeSH C10.597.350.090.500.530.060 --- ataxia telangiectasia
- MeSH C10.597.350.090.500.530.530 --- machado-joseph disease
- MeSH C10.597.350.090.750 --- gait ataxia
- MeSH C10.597.350.110 --- athetosis
- MeSH C10.597.350.200 --- catalepsy
- MeSH C10.597.350.250 --- chorea
- MeSH C10.597.350.300 --- dystonia
- MeSH C10.597.350.300.800 --- torticollis
- MeSH C10.597.350.350 --- hyperkinesis
- MeSH C10.597.350.400 --- hypokinesia
- MeSH C10.597.350.500 --- myoclonus
- MeSH C10.597.350.600 --- psychomotor agitation
- MeSH C10.597.350.675 --- synkinesis
- MeSH C10.597.350.700 --- tics
- MeSH C10.597.350.850 --- tremor
MeSH C10.597.404 --- gait disorders, neurologic[sửa]
MeSH C10.597.544 --- meningism[sửa]
MeSH C10.597.606 --- neurobehavioral manifestations[sửa]
- MeSH C10.597.606.115 --- catatonia
- MeSH C10.597.606.150 --- communication disorders
- MeSH C10.597.606.150.500 --- language disorders
- MeSH C10.597.606.150.500.050 --- agraphia
- MeSH C10.597.606.150.500.090 --- anomia
- MeSH C10.597.606.150.500.300 --- dyslexia
- MeSH C10.597.606.150.500.300.200 --- dyslexia, acquired
- MeSH C10.597.606.150.500.300.200.100 --- alexia, pure
- MeSH C10.597.606.150.500.550 --- language development disorders
- MeSH C10.597.606.150.500.800 --- speech disorders
- MeSH C10.597.606.150.500.800.100 --- aphasia
- MeSH C10.597.606.150.500.800.100.100 --- aphasia, broca
- MeSH C10.597.606.150.500.800.100.111 --- aphasia, conduction
- MeSH C10.597.606.150.500.800.100.155 --- aphasia, primary progressive
- MeSH C10.597.606.150.500.800.100.166 --- aphasia, wernicke
- MeSH C10.597.606.150.500.800.150 --- articulation disorders
- MeSH C10.597.606.150.500.800.150.200 --- dysarthria
- MeSH C10.597.606.150.500.800.300 --- echolalia
- MeSH C10.597.606.150.500.800.500 --- mutism
- MeSH C10.597.606.150.500.800.750 --- stuttering
- MeSH C10.597.606.150.550 --- learning disorders
- MeSH C10.597.606.150.550.200 --- dyslexia
- MeSH C10.597.606.150.550.200.500 --- dyslexia, acquired
- MeSH C10.597.606.337 --- confusion
- MeSH C10.597.606.337.500 --- delirium
- MeSH C10.597.606.358 --- consciousness disorders
- MeSH C10.597.606.358.800 --- unconsciousness
- MeSH C10.597.606.358.800.200 --- coma
- MeSH C10.597.606.358.800.200.100 --- brain death
- MeSH C10.597.606.358.800.200.200 --- coma, post-head injury
- MeSH C10.597.606.358.800.200.600 --- insulin coma
- MeSH C10.597.606.358.800.400 --- persistent vegetative state
- MeSH C10.597.606.358.800.600 --- syncope
- MeSH C10.597.606.358.800.600.500 --- syncope, vasovagal
- MeSH C10.597.606.525 --- memory disorders
- MeSH C10.597.606.525.100 --- amnesia
- MeSH C10.597.606.525.100.075 --- amnesia, anterograde
- MeSH C10.597.606.525.100.150 --- amnesia, retrograde
- MeSH C10.597.606.525.100.800 --- amnesia, transient global
- MeSH C10.597.606.525.400 --- korsakoff syndrome
- MeSH C10.597.606.643 --- mental retardation
- MeSH C10.597.606.643.180 --- cri-du-chat syndrome
- MeSH C10.597.606.643.210 --- de lange syndrome
- MeSH C10.597.606.643.220 --- down syndrome
- MeSH C10.597.606.643.455 --- mental retardation, x-linked
- MeSH C10.597.606.643.455.124 --- adrenoleukodystrophy
- MeSH C10.597.606.643.455.249 --- coffin-lowry syndrome
- MeSH C10.597.606.643.455.500 --- fragile x syndrome
- MeSH C10.597.606.643.455.562 --- glycogen storage disease type iib
- MeSH C10.597.606.643.455.625 --- lesch-nyhan syndrome
- MeSH C10.597.606.643.455.687 --- menkes kinky hair syndrome
- MeSH C10.597.606.643.455.750 --- mucopolysaccharidosis ii
- MeSH C10.597.606.643.455.875 --- pyruvate dehydrogenase complex deficiency disease
- MeSH C10.597.606.643.455.937 --- rett syndrome
- MeSH C10.597.606.643.690 --- prader-willi syndrome
- MeSH C10.597.606.643.700 --- rubinstein-taybi syndrome
- MeSH C10.597.606.643.969 --- wagr syndrome
- MeSH C10.597.606.643.970 --- williams syndrome
- MeSH C10.597.606.762 --- perceptual disorders
- MeSH C10.597.606.762.100 --- agnosia
- MeSH C10.597.606.762.100.300 --- gerstmann syndrome
- MeSH C10.597.606.762.100.650 --- prosopagnosia
- MeSH C10.597.606.762.200 --- auditory perceptual disorders
- MeSH C10.597.606.762.300 --- hallucinations
- MeSH C10.597.606.762.400 --- illusions
- MeSH C10.597.606.762.700 --- phantom limb
- MeSH C10.597.606.881 --- psychomotor disorders
- MeSH C10.597.606.881.350 --- apraxias
- MeSH C10.597.606.881.350.200 --- apraxia, ideomotor
- MeSH C10.597.606.881.350.600 --- gait apraxia
- MeSH C10.597.606.881.700 --- psychomotor agitation
MeSH C10.597.609 --- neurogenic inflammation[sửa]
MeSH C10.597.613 --- neuromuscular manifestations[sửa]
- MeSH C10.597.613.250 --- fasciculation
- MeSH C10.597.613.500 --- muscle cramp
- MeSH C10.597.613.550 --- muscle hypertonia
- MeSH C10.597.613.550.500 --- muscle rigidity
- MeSH C10.597.613.550.550 --- muscle spasticity
- MeSH C10.597.613.575 --- muscle hypotonia
- MeSH C10.597.613.593 --- muscle weakness
- MeSH C10.597.613.612 --- muscular atrophy
- MeSH C10.597.613.650 --- myokymia
- MeSH C10.597.613.700 --- myotonia
- MeSH C10.597.613.750 --- spasm
- MeSH C10.597.613.750.400 --- hemifacial spasm
- MeSH C10.597.613.750.700 --- trismus
- MeSH C10.597.613.875 --- tetany
MeSH C10.597.617 --- pain[sửa]
- MeSH C10.597.617.152 --- back pain
- MeSH C10.597.617.152.400 --- low back pain
- MeSH C10.597.617.364 --- facial pain
- MeSH C10.597.617.470 --- headache
- MeSH C10.597.617.515 --- labor pain
- MeSH C10.597.617.560 --- metatarsalgia
- MeSH C10.597.617.576 --- neck pain
- MeSH C10.597.617.682 --- neuralgia
- MeSH C10.597.617.682.550 --- neuralgia, postherpetic
- MeSH C10.597.617.682.800 --- sciatica
- MeSH C10.597.617.788 --- pain, intractable
MeSH C10.597.622 --- paralysis[sửa]
- MeSH C10.597.622.214 --- facial paralysis
- MeSH C10.597.622.295 --- hemiplegia
- MeSH C10.597.622.447 --- ophthalmoplegia
- MeSH C10.597.622.447.511 --- ophthalmoplegia, chronic progressive external
- MeSH C10.597.622.447.690 --- supranuclear palsy, progressive
- MeSH C10.597.622.669 --- paraplegia
- MeSH C10.597.622.669.300 --- brown-sequard syndrome
- MeSH C10.597.622.714 --- pseudobulbar palsy
- MeSH C10.597.622.760 --- quadriplegia
- MeSH C10.597.622.812 --- respiratory paralysis
- MeSH C10.597.622.943 --- vocal cord paralysis
MeSH C10.597.636 --- paresis[sửa]
MeSH C10.597.690 --- pupil disorders[sửa]
- MeSH C10.597.690.150 --- anisocoria
- MeSH C10.597.690.362 --- miosis
- MeSH C10.597.690.362.500 --- horner syndrome
- MeSH C10.597.690.575 --- tonic pupil
MeSH C10.597.704 --- reflex, abnormal[sửa]
MeSH C10.597.742 --- seizures[sửa]
MeSH C10.597.751 --- sensation disorders[sửa]
- MeSH C10.597.751.237 --- dizziness
- MeSH C10.597.751.418 --- hearing disorders
- MeSH C10.597.751.418.341 --- hearing loss
- MeSH C10.597.751.418.341.186 --- deafness
- MeSH C10.597.751.418.341.374 --- hearing loss, bilateral
- MeSH C10.597.751.418.341.562 --- hearing loss, conductive
- MeSH C10.597.751.418.341.750 --- hearing loss, functional
- MeSH C10.597.751.418.341.812 --- hearing loss, high-frequency
- MeSH C10.597.751.418.341.849 --- hearing loss, mixed conductive-sensorineural
- MeSH C10.597.751.418.341.887 --- hearing loss, sensorineural
- MeSH C10.597.751.418.341.887.432 --- hearing loss, central
- MeSH C10.597.751.418.341.887.460 --- hearing loss, noise-induced
- MeSH C10.597.751.418.341.887.772 --- presbycusis
- MeSH C10.597.751.418.341.887.886 --- usher syndromes
- MeSH C10.597.751.418.341.900 --- hearing loss, sudden
- MeSH C10.597.751.418.341.950 --- hearing loss, unilateral
- MeSH C10.597.751.418.505 --- hyperacusis
- MeSH C10.597.751.418.670 --- tinnitus
- MeSH C10.597.751.600 --- olfaction disorders
- MeSH C10.597.751.791 --- somatosensory disorders
- MeSH C10.597.751.791.400 --- hyperalgesia
- MeSH C10.597.751.791.450 --- hyperesthesia
- MeSH C10.597.751.791.500 --- hypesthesia
- MeSH C10.597.751.791.875 --- paresthesia
- MeSH C10.597.751.861 --- taste disorders
- MeSH C10.597.751.861.184 --- ageusia
- MeSH C10.597.751.861.479 --- dysgeusia
- MeSH C10.597.751.941 --- vision disorders
- MeSH C10.597.751.941.073 --- amblyopia
- MeSH C10.597.751.941.162 --- blindness
- MeSH C10.597.751.941.162.125 --- amaurosis fugax
- MeSH C10.597.751.941.162.250 --- blindness, cortical
- MeSH C10.597.751.941.256 --- color vision defects
- MeSH C10.597.751.941.339 --- diplopia
- MeSH C10.597.751.941.512 --- hemianopsia
- MeSH C10.597.751.941.661 --- photophobia
- MeSH C10.597.751.941.811 --- scotoma
- MeSH C10.597.751.941.905 --- vision, low
MeSH C10.597.951 --- vertigo[sửa]
MeSH C10.597.975 --- voice disorders[sửa]
MeSH C10.668 --- neuromuscular diseases[sửa]
MeSH C10.668.364 --- fatigue syndrome, chronic[sửa]
MeSH C10.668.402 --- isaacs syndrome[sửa]
MeSH C10.668.460 --- motor neuron disease[sửa]
- MeSH C10.668.460.250 --- amyotrophic lateral sclerosis
- MeSH C10.668.460.300 --- bulbar palsy, progressive
- MeSH C10.668.460.500 --- muscular atrophy, spinal
- MeSH C10.668.460.500.750 --- spinal muscular atrophies of childhood
- MeSH C10.668.460.600 --- poliomyelitis
- MeSH C10.668.460.600.500 --- postpoliomyelitis syndrome
MeSH C10.668.475 --- muscular atrophy, spinal[sửa]
MeSH C10.668.491 --- muscular diseases[sửa]
- MeSH C10.668.491.175 --- muscular disorders, atrophic
- MeSH C10.668.491.175.500 --- muscular dystrophies
- MeSH C10.668.491.175.500.074 --- distal myopathies
- MeSH C10.668.491.175.500.149 --- muscular dystrophies, limb-girdle
- MeSH C10.668.491.175.500.300 --- muscular dystrophy, duchenne
- MeSH C10.668.491.175.500.350 --- muscular dystrophy, emery-dreifuss
- MeSH C10.668.491.175.500.400 --- muscular dystrophy, facioscapulohumeral
- MeSH C10.668.491.175.500.450 --- muscular dystrophy, oculopharyngeal
- MeSH C10.668.491.175.500.500 --- myotonic dystrophy
- MeSH C10.668.491.175.750 --- postpoliomyelitis syndrome
- MeSH C10.668.491.387 --- eosinophilia-myalgia syndrome
- MeSH C10.668.491.425 --- fibromyalgia
- MeSH C10.668.491.500 --- mitochondrial myopathies
- MeSH C10.668.491.500.500 --- mitochondrial encephalomyopathies
- MeSH C10.668.491.500.500.500 --- melas syndrome
- MeSH C10.668.491.500.500.550 --- merrf syndrome
- MeSH C10.668.491.500.700 --- ophthalmoplegia, chronic progressive external
- MeSH C10.668.491.500.700.500 --- kearns-sayer syndrome
- MeSH C10.668.491.550 --- myopathies, structural, congenital
- MeSH C10.668.491.550.290 --- myopathies, nemaline
- MeSH C10.668.491.550.300 --- myopathy, central core
- MeSH C10.668.491.562 --- myositis
- MeSH C10.668.491.562.150 --- dermatomyositis
- MeSH C10.668.491.562.500 --- myositis, inclusion body
- MeSH C10.668.491.562.575 --- polymyositis
- MeSH C10.668.491.562.575.500 --- dermatomyositis
- MeSH C10.668.491.606 --- myotonic disorders
- MeSH C10.668.491.606.500 --- myotonia congenita
- MeSH C10.668.491.606.750 --- myotonic dystrophy
- MeSH C10.668.491.650 --- paralyses, familial periodic
- MeSH C10.668.491.650.450 --- hypokalemic periodic paralysis
- MeSH C10.668.491.650.600 --- paralysis, hyperkalemic periodic
MeSH C10.668.550 --- muscular disorders, atrophic[sửa]
MeSH C10.668.758 --- neuromuscular junction diseases[sửa]
- MeSH C10.668.758.200 --- botulism
- MeSH C10.668.758.450 --- lambert-eaton myasthenic syndrome
- MeSH C10.668.758.725 --- myasthenia gravis
- MeSH C10.668.758.725.300 --- myasthenia gravis, autoimmune, experimental
- MeSH C10.668.758.725.650 --- myasthenia gravis, neonatal
- MeSH C10.668.758.800 --- myasthenic syndromes, congenital
MeSH C10.668.829 --- peripheral nervous system diseases[sửa]
- MeSH C10.668.829.025 --- acrodynia
- MeSH C10.668.829.050 --- amyloid neuropathies
- MeSH C10.668.829.050.050 --- amyloid neuropathies, familial
- MeSH C10.668.829.100 --- brachial plexus neuropathies
- MeSH C10.668.829.100.500 --- brachial plexus neuritis
- MeSH C10.668.829.250 --- complex regional pain syndromes
- MeSH C10.668.829.250.200 --- causalgia
- MeSH C10.668.829.250.800 --- reflex sympathetic dystrophy
- MeSH C10.668.829.300 --- diabetic neuropathies
- MeSH C10.668.829.350 --- guillain-barre syndrome
- MeSH C10.668.829.350.500 --- miller fisher syndrome
- MeSH C10.668.829.425 --- isaacs syndrome
- MeSH C10.668.829.500 --- mononeuropathies
- MeSH C10.668.829.500.200 --- femoral neuropathy
- MeSH C10.668.829.500.500 --- median neuropathy
- MeSH C10.668.829.500.500.200 --- carpal tunnel syndrome
- MeSH C10.668.829.500.600 --- peroneal neuropathies
- MeSH C10.668.829.500.650 --- radial neuropathy
- MeSH C10.668.829.500.675 --- sciatic neuropathy
- MeSH C10.668.829.500.675.800 --- sciatica
- MeSH C10.668.829.500.700 --- tibial neuropathy
- MeSH C10.668.829.500.700.800 --- tarsal tunnel syndrome
- MeSH C10.668.829.500.850 --- ulnar neuropathies
- MeSH C10.668.829.500.850.200 --- cubital tunnel syndrome
- MeSH C10.668.829.500.850.600 --- ulnar nerve compression syndromes
- MeSH C10.668.829.550 --- nerve compression syndromes
- MeSH C10.668.829.550.200 --- carpal tunnel syndrome
- MeSH C10.668.829.550.800 --- tarsal tunnel syndrome
- MeSH C10.668.829.550.850 --- thoracic outlet syndrome
- MeSH C10.668.829.550.850.200 --- cervical rib syndrome
- MeSH C10.668.829.550.925 --- ulnar nerve compression syndromes
- MeSH C10.668.829.550.925.200 --- cubital tunnel syndrome
- MeSH C10.668.829.600 --- neuralgia
- MeSH C10.668.829.600.200 --- causalgia
- MeSH C10.668.829.600.550 --- neuralgia, postherpetic
- MeSH C10.668.829.600.800 --- sciatica
- MeSH C10.668.829.650 --- neuritis
- MeSH C10.668.829.650.250 --- brachial plexus neuritis
- MeSH C10.668.829.650.500 --- neuritis, autoimmune, experimental
- MeSH C10.668.829.675 --- neurofibromatosis 1
- MeSH C10.668.829.700 --- pain insensitivity, congenital
- MeSH C10.668.829.725 --- peripheral nervous system neoplasms
- MeSH C10.668.829.725.500 --- nerve sheath neoplasms
- MeSH C10.668.829.725.500.500 --- neurilemmoma
- MeSH C10.668.829.725.500.600 --- neurofibroma
- MeSH C10.668.829.725.500.600.500 --- neurofibroma, plexiform
- MeSH C10.668.829.725.500.600.600 --- neurofibrosarcoma
- MeSH C10.668.829.800 --- polyneuropathies
- MeSH C10.668.829.800.050 --- alcoholic neuropathy
- MeSH C10.668.829.800.300 --- hereditary motor and sensory neuropathies
- MeSH C10.668.829.800.300.200 --- charcot-marie-tooth disease
- MeSH C10.668.829.800.300.780 --- refsum disease
- MeSH C10.668.829.800.300.820 --- spastic paraplegia, hereditary
- MeSH C10.668.829.800.625 --- hereditary sensory and autonomic neuropathies
- MeSH C10.668.829.800.625.200 --- dysautonomia, familial
- MeSH C10.668.829.800.662 --- paraneoplastic polyneuropathy
- MeSH C10.668.829.800.700 --- poems syndrome
- MeSH C10.668.829.800.750 --- polyradiculoneuropathy
- MeSH C10.668.829.800.750.300 --- guillain-barre syndrome
- MeSH C10.668.829.800.750.300.500 --- miller fisher syndrome
- MeSH C10.668.829.800.750.450 --- hereditary sensory and autonomic neuropathies
- MeSH C10.668.829.800.750.450.250 --- dysautonomia, familial
- MeSH C10.668.829.800.750.600 --- polyradiculoneuropathy, chronic inflammatory demyelinating
- MeSH C10.668.829.800.750.700 --- polyradiculopathy
- MeSH C10.668.829.800.750.700.700 --- radiculopathy
- MeSH C10.668.829.800.875 --- tangier disease
MeSH C10.668.900 --- stiff-person syndrome[sửa]
MeSH C10.720 --- neurotoxicity syndromes[sửa]
MeSH C10.720.075 --- akathisia, drug-induced[sửa]
MeSH C10.720.112 --- alcohol-induced disorders, nervous system[sửa]
- MeSH C10.720.112.100 --- alcohol amnestic disorder
- MeSH C10.720.112.100.500 --- korsakoff syndrome
- MeSH C10.720.112.200 --- alcohol withdrawal delirium
- MeSH C10.720.112.300 --- alcohol withdrawal seizures
- MeSH C10.720.112.400 --- alcoholic neuropathy
MeSH C10.720.150 --- botulism[sửa]
MeSH C10.720.312 --- dyskinesia, drug-induced[sửa]
MeSH C10.720.475 --- heavy metal poisoning, nervous system[sửa]
- MeSH C10.720.475.150 --- arsenic poisoning
- MeSH C10.720.475.400 --- lead poisoning, nervous system
- MeSH C10.720.475.400.350 --- lead poisoning, nervous system, adult
- MeSH C10.720.475.400.700 --- lead poisoning, nervous system, childhood
- MeSH C10.720.475.500 --- manganese poisoning
- MeSH C10.720.475.600 --- mercury poisoning, nervous system
- MeSH C10.720.475.600.150 --- acrodynia
MeSH C10.720.606 --- mptp poisoning[sửa]
MeSH C10.720.737 --- neuroleptic malignant syndrome[sửa]
MeSH C10.886 --- sleep disorders[sửa]
MeSH C10.886.425 --- dyssomnias[sửa]
- MeSH C10.886.425.175 --- sleep deprivation
- MeSH C10.886.425.200 --- sleep disorders, circadian rhythm
- MeSH C10.886.425.200.500 --- jet lag syndrome
- MeSH C10.886.425.800 --- sleep disorders, intrinsic
- MeSH C10.886.425.800.200 --- disorders of excessive somnolence
- MeSH C10.886.425.800.200.400 --- hypersomnolence, idiopathic
- MeSH C10.886.425.800.200.500 --- kleine-levin syndrome
- MeSH C10.886.425.800.200.750 --- narcolepsy
- MeSH C10.886.425.800.200.750.500 --- cataplexy
- MeSH C10.886.425.800.600 --- nocturnal myoclonus syndrome
- MeSH C10.886.425.800.700 --- restless legs syndrome
- MeSH C10.886.425.800.750 --- sleep apnea syndromes
- MeSH C10.886.425.800.750.800 --- sleep apnea, central
- MeSH C10.886.425.800.750.850 --- sleep apnea, obstructive
- MeSH C10.886.425.800.750.850.500 --- obesity hypoventilation syndrome
- MeSH C10.886.425.800.800 --- sleep initiation and maintenance disorders
- MeSH C10.886.425.800.800.400 --- insomnia, fatal familial
MeSH C10.886.659 --- parasomnias[sửa]
- MeSH C10.886.659.618 --- nocturnal myoclonus syndrome
- MeSH C10.886.659.627 --- nocturnal paroxysmal dystonia
- MeSH C10.886.659.633 --- rem sleep parasomnias
- MeSH C10.886.659.633.700 --- rem sleep behavior disorder
- MeSH C10.886.659.633.800 --- sleep paralysis
- MeSH C10.886.659.634 --- restless legs syndrome
- MeSH C10.886.659.635 --- sleep arousal disorders
- MeSH C10.886.659.635.600 --- night terrors
- MeSH C10.886.659.635.700 --- somnambulism
- MeSH C10.886.659.637 --- sleep bruxism
- MeSH C10.886.659.700 --- sleep-wake transition disorders
MeSH C10.900 --- trauma, nervous system[sửa]
MeSH C10.900.250 --- cerebrovascular trauma[sửa]
- MeSH C10.900.250.300 --- carotid artery injuries
- MeSH C10.900.250.300.300 --- carotid artery, internal, dissection
- MeSH C10.900.250.300.400 --- carotid-cavernous sinus fistula
- MeSH C10.900.250.650 --- vertebral artery dissection
MeSH C10.900.300 --- craniocerebral trauma[sửa]
- MeSH C10.900.300.087 --- brain injuries
- MeSH C10.900.300.087.125 --- brain concussion
- MeSH C10.900.300.087.125.500 --- post-concussion syndrome
- MeSH C10.900.300.087.187 --- brain hemorrhage, traumatic
- MeSH C10.900.300.087.187.200 --- brain stem hemorrhage, traumatic
- MeSH C10.900.300.087.187.300 --- cerebral hemorrhage, traumatic
- MeSH C10.900.300.087.250 --- brain injury, chronic
- MeSH C10.900.300.087.500 --- diffuse axonal injury
- MeSH C10.900.300.087.600 --- epilepsy, post-traumatic
- MeSH C10.900.300.087.700 --- pneumocephalus
- MeSH C10.900.300.087.850 --- shaken baby syndrome
- MeSH C10.900.300.131 --- cerebrospinal fluid otorrhea
- MeSH C10.900.300.153 --- cerebrospinal fluid rhinorrhea
- MeSH C10.900.300.175 --- coma, post-head injury
- MeSH C10.900.300.218 --- cranial nerve injuries
- MeSH C10.900.300.218.150 --- abducens nerve injury
- MeSH C10.900.300.218.300 --- facial nerve injuries
- MeSH C10.900.300.218.550 --- optic nerve injuries
- MeSH C10.900.300.350 --- head injuries, closed
- MeSH C10.900.300.350.300 --- brain concussion
- MeSH C10.900.300.350.300.500 --- post-concussion syndrome
- MeSH C10.900.300.675 --- head injuries, penetrating
- MeSH C10.900.300.837 --- intracranial hemorrhage, traumatic
- MeSH C10.900.300.837.150 --- brain hemorrhage, traumatic
- MeSH C10.900.300.837.150.300 --- brain stem hemorrhage, traumatic
- MeSH C10.900.300.837.150.650 --- cerebral hemorrhage, traumatic
- MeSH C10.900.300.837.300 --- hematoma, epidural, cranial
- MeSH C10.900.300.837.600 --- hematoma, subdural
- MeSH C10.900.300.837.600.050 --- hematoma, subdural, acute
- MeSH C10.900.300.837.600.120 --- hematoma, subdural, chronic
- MeSH C10.900.300.837.600.400 --- hematoma, subdural, intracranial
- MeSH C10.900.300.837.800 --- subarachnoid hemorrhage, traumatic
- MeSH C10.900.300.918 --- skull fractures
- MeSH C10.900.300.918.150 --- skull fracture, basilar
- MeSH C10.900.300.918.300 --- skull fracture, depressed