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List of MeSH codes (C10)

Summary

The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).

This list continues the information at List of MeSH codes (C09). Codes following these are found at List of MeSH codes (C11). For other MeSH codes, see List of MeSH codes.

The source for this content is the set of 2006 MeSH Trees from the NLM.

MeSH C10 – nervous system diseases edit

MeSH C10.114 – autoimmune diseases of the nervous system edit

MeSH C10.114.375 – demyelinating autoimmune diseases, cns edit

MeSH C10.114.468 – lambert-eaton myasthenic syndrome edit

MeSH C10.114.562 – leukoencephalitis, acute hemorrhagic edit

MeSH C10.114.656 – myasthenia gravis edit

  • 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 edit

MeSH C10.114.750 – polyradiculoneuropathy edit

MeSH C10.114.812 – stiff-person syndrome edit

MeSH C10.114.843 – uveomeningoencephalitic syndrome edit

MeSH C10.114.875 – vasculitis, central nervous system edit

MeSH C10.177 – autonomic nervous system diseases edit

MeSH C10.177.045 – aide syndrome edit

MeSH C10.177.090 – autonomic dysreflexia edit

MeSH C10.177.195 – complex regional pain syndromes edit

MeSH C10.177.272 – dysautonomia, familial edit

MeSH C10.177.350 – horner syndrome edit

MeSH C10.177.800 – shy-drager syndrome edit

MeSH C10.177.825 – sweating, gustatory edit

MeSH C10.228 – central nervous system diseases edit

MeSH C10.228.140 – brain diseases edit

MeSH C10.228.228 – central nervous system infections edit

MeSH C10.228.440 – encephalomyelitis edit

MeSH C10.228.470 – high pressure neurological syndrome edit

MeSH C10.228.566 – meningitis edit

MeSH C10.228.662 – movement disorders edit

MeSH C10.228.758 – ocular motility disorders edit

MeSH C10.228.806 – pneumocephalus edit

MeSH C10.228.854 – spinal cord diseases edit

MeSH C10.281 – chronobiology disorders edit

MeSH C10.281.440 – jet lag syndrome edit

MeSH C10.281.800 – sleep disorders, circadian rhythm edit

MeSH C10.292 – cranial nerve diseases edit

MeSH C10.292.150 – abducens nerve diseases edit

MeSH C10.292.175 – accessory nerve diseases edit

MeSH C10.292.225 – cranial nerve neoplasms edit

MeSH C10.292.262 – cranial nerve injuries edit

MeSH C10.292.300 – facial nerve diseases edit

MeSH C10.292.375 – facial neuralgia edit

MeSH C10.292.450 – glossopharyngeal nerve diseases edit

MeSH C10.292.525 – hypoglossal nerve diseases edit

MeSH C10.292.562 – ocular motility disorders edit

MeSH C10.292.600 – oculomotor nerve diseases edit

  • MeSH C10.292.600.200 – aide syndrome

MeSH C10.292.650 – olfactory nerve diseases edit

MeSH C10.292.700 – optic nerve diseases edit

MeSH C10.292.775 – trigeminal nerve diseases edit

MeSH C10.292.850 – trochlear nerve diseases edit

MeSH C10.292.887 – vagus nerve diseases edit

MeSH C10.292.910 – vestibulocochlear nerve diseases edit

MeSH C10.314 – demyelinating diseases edit

MeSH C10.314.350 – demyelinating autoimmune diseases, cns edit

MeSH C10.314.400 – hereditary central nervous system demyelinating diseases edit

MeSH C10.314.450 – leukoencephalopathy, progressive multifocal edit

MeSH C10.314.500 – myelinolysis, central pontine edit

MeSH C10.314.750 – polyradiculoneuropathy edit

MeSH C10.500 – nervous system malformations edit

MeSH C10.500.142 – central nervous system cysts edit

MeSH C10.500.190 – central nervous system vascular malformations edit

MeSH C10.500.205 – dandy-walker syndrome edit

MeSH C10.500.300 – hereditary motor and sensory neuropathies edit

MeSH C10.500.310 – hereditary sensory and autonomic neuropathies edit

MeSH C10.500.410 – holoprosencephaly edit

MeSH C10.500.450 – hydranencephaly edit

MeSH C10.500.460 – intracranial arteriovenous malformations edit

MeSH C10.500.680 – neural tube defects edit

MeSH C10.500.840 – septo-optic dysplasia edit

MeSH C10.551 – nervous system neoplasms edit

MeSH C10.551.240 – central nervous system neoplasms edit

MeSH C10.551.360 – cranial nerve neoplasms edit

MeSH C10.551.525 – neuroma, acoustic edit

MeSH C10.551.775 – peripheral nervous system neoplasms edit

MeSH C10.562 – neurocutaneous syndromes edit

MeSH C10.562.100 – ataxia telangiectasia edit

MeSH C10.562.400 – hippel-lindau disease edit

MeSH C10.562.600 – neurofibromatosis edit

MeSH C10.562.800 – sturge-weber syndrome edit

MeSH C10.562.850 – tuberous sclerosis edit

MeSH C10.574 – neurodegenerative diseases edit

MeSH C10.574.500 – heredodegenerative disorders, nervous system edit

MeSH C10.574.531 – lewy body disease edit

MeSH C10.574.562 – motor neuron disease edit

MeSH C10.574.625 – multiple system atrophy edit

MeSH C10.574.750 – olivopontocerebellar atrophies edit

MeSH C10.574.781 – paraneoplastic syndromes, nervous system edit

MeSH C10.574.812 – parkinson disease edit

MeSH C10.574.827 – postpoliomyelitis syndrome edit

MeSH C10.574.843 – prion diseases edit

MeSH C10.574.875 – shy-drager syndrome edit

MeSH C10.574.945 – tauopathies edit

MeSH C10.597 – neurologic manifestations edit

MeSH C10.597.200 – bladder, neurogenic edit

MeSH C10.597.230 – cerebrospinal fluid otorrhea edit

MeSH C10.597.267 – cerebrospinal fluid rhinorrhea edit

MeSH C10.597.305 – decerebrate state edit

MeSH C10.597.350 – dyskinesias edit

MeSH C10.597.404 – gait disorders, neurologic edit

MeSH C10.597.544 – meningism edit

MeSH C10.597.606 – neurobehavioral manifestations edit

MeSH C10.597.609 – neurogenic inflammation edit

MeSH C10.597.613 – neuromuscular manifestations edit

MeSH C10.597.617 – pain edit

MeSH C10.597.622 – paralysis edit

MeSH C10.597.636 – paresis edit

MeSH C10.597.690 – pupil disorders edit

MeSH C10.597.704 – reflex, abnormal edit

MeSH C10.597.742 – seizures edit

MeSH C10.597.751 – sensation disorders edit

MeSH C10.597.951 – vertigo edit

MeSH C10.597.975 – voice disorders edit

MeSH C10.668 – neuromuscular diseases edit

MeSH C10.668.364 – fatigue syndrome, chronic edit

MeSH C10.668.402 – isaacs syndrome edit

MeSH C10.668.460 – motor neuron disease edit

MeSH C10.668.475 – muscular atrophy, spinal edit

MeSH C10.668.491 – muscular diseases edit

MeSH C10.668.550 – muscular disorders, atrophic edit

MeSH C10.668.758 – neuromuscular junction diseases edit

MeSH C10.668.829 – peripheral nervous system diseases edit

MeSH C10.668.900 – stiff-person syndrome edit

MeSH C10.720 – neurotoxicity syndromes edit

MeSH C10.720.075 – akathisia, drug-induced edit

MeSH C10.720.112 – alcohol-induced disorders, nervous system edit

MeSH C10.720.150 – botulism edit

MeSH C10.720.312 – dyskinesia, drug-induced edit

MeSH C10.720.475 – heavy metal poisoning, nervous system edit

MeSH C10.720.606 – mptp poisoning edit

MeSH C10.720.737 – neuroleptic malignant syndrome edit

MeSH C10.886 – sleep disorders edit

MeSH C10.886.425 – dyssomnias edit

MeSH C10.886.659 – parasomnias edit

MeSH C10.900 – trauma, nervous system edit

MeSH C10.900.250 – cerebrovascular trauma edit

MeSH C10.900.300 – craniocerebral trauma edit

MeSH C10.900.850 – spinal cord injuries edit

The list continues at List of MeSH codes (C11).

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