ICD-10 Chapter VI: Diseases of the nervous system
G00-G99 – Diseases of the nervous system
G00-G99 – Diseases of the nervous system
(G00-G09) Inflammatory diseases of the central nervous system
- (G00) Bacterial meningitis, not elsewhere classified
- (G00.0) Haemophilus meningitis
- (G00.1) Pneumococcal meningitis
- (G00.2) Streptococcal meningitis
- (G00.3) Staphylococcal meningitis
- (G00.8) Other bacterial meningitis
- Meningitis due to Escherichia coli
- Meningitis due to Friedländer bacillus
- Meningitis due to Klebsiella
- (G00.9) Bacterial meningitis, unspecified
- (G01) Meningitis in bacterial diseases classified elsewhere
- (G02) Meningitis in other infectious and parasitic diseases classified elsewhere
- (G03) Meningitis due to other and unspecified causes
- (G03.0) Nonpyogenic meningitis
- (G03.1) Chronic meningitis
- (G03.2) Benign recurrent meningitis (Mollaret)
- (G03.8) Meningitis due to other specified causes
- (G03.9) Meningitis, unspecified
- Arachnoiditis (spinal) NOS
- (G04) Encephalitis, myelitis and encephalomyelitis
- (G04.0) Acute disseminated encephalitis
- (G04.1) Tropical spastic paraplegia
- (G04.2) Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
- (G04.8) Other encephalitis, myelitis and encephalomyelitis
- (G04.9) Encephalitis, myelitis and encephalomyelitis, unspecified
- (G05) Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere
- (G06) Intracranial and intraspinal abscess and granuloma
- (G07) Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
- (G08) Intracranial and intraspinal phlebitis and thrombophlebitis
- (G09) Sequelae of inflammatory diseases of central nervous system
(G10-G13) Systemic atrophies primarily affecting the central nervous system
- (G11) Hereditary ataxia
- (G11.0) Congenital nonprogressive ataxia
- (G11.1) Early-onset cerebellar ataxia
- (G11.2) Late-onset cerebellar ataxia
- (G11.3) Cerebellar ataxia with defective DNA repair
- Ataxia telangiectasia (Louis-Bar)
- (G11.4) Hereditary spastic paraplegia
- (G11.8) Other hereditary ataxias
- (G11.9) Hereditary ataxia, unspecified
- (G12) Spinal muscular atrophy and related syndromes
- (G12.0) Werdnig-Hoffman disease (Type 1)
- (G12.1) Other inherited spinal muscular atrophy
- (G12.2) Motor neuron disease
- (G13) Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
- (G13.0) Paraneoplastic neuromyopathy and neuropathy
- (G13.1) Other systemic atrophy primarily affecting central nervous system in neoplastic disease
- (G13.2) Systemic atrophy primarily affecting central nervous system in myxoedema
- (G13.8) Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
(G20-G26) Extrapyramidal and movement disorders
- (G22) Parkinsonism in diseases classified elsewhere
- (G23) Other degenerative diseases of basal ganglia
- (G23.0) Hallervorden-Spatz disease
- (G23.1) Progressive supranuclear ophthalmoplegia (Steele-Richardson-Olszewski)
- (G23.2) Striatonigral degeneration
- (G23.8) Other specified degenerative diseases of basal ganglia
- (G23.9) Degenerative disease of basal ganglia, unspecified
- (G25) Other extrapyramidal and movement disorders
- (G25.0) Essential tremor
- (G25.1) Drug-induced tremor
- (G25.2) Other specified forms of tremor
- (G25.3) Myoclonus
- (G25.4) Drug-induced chorea
- (G25.5) Other chorea
- (G25.6) Drug-induced tics and other tics of organic origin
- (G25.8) Other specified extrapyramidal and movement disorders
- (G25.9) Extrapyramidal and movement disorder, unspecified
- (G26) Extrapyramidal and movement disorders in diseases classified elsewhere
(G30-G32) Other degenerative diseases of the nervous system
- (G31) Other degenerative diseases of nervous system, not elsewhere classified
- (G31.0) Circumscribed brain atrophy
- (G31.1) Senile degeneration of brain, not elsewhere classified
- (G31.2) Degeneration of nervous system due to alcohol
- (G31.8) Other specified degenerative diseases of nervous system
- (G31.9) Degenerative disease of nervous system, unspecified
- (G32) Other degenerative disorders of nervous system in diseases classified elsewhere
- (G32.0) Subacute combined degeneration of spinal cord in diseases classified elsewhere
- (G32.8) Other specified degenerative disorders of nervous system in diseases classified elsewhere
(G35-G37) Demyelinating diseases of the central nervous system
- (G36) Other acute disseminated demyelination
- (G36.0) Neuromyelitis optica (Devic)
- (G36.1) Acute and subacute haemorrhagic leukoencephalitis (Hurst)
- (G36.8) Other specified acute disseminated demyelination
- (G36.9) Acute disseminated demyelination, unspecified
- (G37) Other demyelinating diseases of central nervous system
- (G37.0) Diffuse sclerosis
- (G37.1) Central demyelination of corpus callosum
- (G37.2) Central pontine myelinolysis
- (G37.3) Acute transverse myelitis in demyelinating disease of central nervous system
- (G37.4) Subacute necrotizing myelitis
- (G37.5) Concentric sclerosis (Baló)
- (G37.8) Other specified demyelinating diseases of central nervous system
- (G37.9) Demyelinating disease of central nervous system, unspecified
(G40-G47) Episodic and paroxysmal disorders
- (G40) Epilepsy
- (G40.0) Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
- (G40.1) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
- (G40.2) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
- (G40.3) Generalized idiopathic epilepsy and epileptic syndromes
- Benign:
- myoclonic epilepsy in infancy
- neonatal convulsions (familial)
- Childhood absence epilepsy (pyknolepsy)
- Epilepsy with grand mal seizures on awakening
- Juvenile:
- absence epilepsy
- myoclonic epilepsy (impulsive petit mal)
- Nonspecific epileptic seizures:
- Benign:
- (G40.4) Other generalized epilepsy and epileptic syndromes
- (G40.5) Special epileptic syndromes
- (G40.6) Grand mal seizures, unspecified (with or without petit mal)
- (G40.7) Petit mal, unspecified, without grand mal seizures
- (G40.8) Other epilepsy
- Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized
- (G40.9) Epilepsy, unspecified
- (G41) Status epilepticus
- (G41.0) Grand mal status epilepticus
- (G41.1) Petit mal status epilepticus
- (G41.2) Complex partial status epilepticus
- (G41.8) Other status epilepticus
- (G41.9) Status epilepticus, unspecified
- (G43) Migraine
- (G43.0) Migraine without aura (common migraine)
- (G43.1) Migraine with aura (classical migraine)
- (G43.2) Status migrainosus
- (G43.3) Complicated migraine
- (G43.8) Other migraine
- (G43.9) Migraine, unspecified
- (G44) Other headache syndromes
- (G44.0) Cluster headache syndrome
- (G44.1) Vascular headache, not elsewhere classified
- (G44.2) Tension-type headache
- (G44.3) Chronic post-traumatic headache
- (G44.4) Drug-induced headache, not elsewhere classified
- (G44.8) Other specified headache syndromes
- (G45) Transient cerebral ischaemic attacks and related syndromes
- (G45.0) Vertebro-basilar artery syndrome
- (G45.1) Carotid artery syndrome (hemispheric)
- (G45.2) Multiple and bilateral precerebral artery syndromes
- (G45.3) Amaurosis fugax
- (G45.4) Transient global amnesia
- (G45.8) Other transient cerebral ischaemic attacks and related syndromes
- (G45.9) Transient cerebral ischaemic attack, unspecified
- (G46) Vascular syndromes of brain in cerebrovascular diseases
- (G46.0) Middle cerebral artery syndrome
- (G46.1) Anterior cerebral artery syndrome
- (G46.2) Posterior cerebral artery syndrome
- (G46.3) Brain stem stroke syndrome
- (G46.4) Cerebellar stroke syndrome
- (G46.5) Pure motor lacunar syndrome
- (G46.6) Pure sensory lacunar syndrome
- (G46.7) Other lacunar syndromes
- (G46.8) Other vascular syndromes of brain in cerebrovascular diseases
- (G47) Sleep disorders
- (G47.0) Disorders of initiating and maintaining sleep (insomnias)
- (G47.1) Disorders of excessive somnolence (hypersomnias)
- (G47.2) Disruptions in circadian rhythm including jet lag
- (G47.3) Sleep apnoea
- (G47.4) Narcolepsy and cataplexy
(G50-G59) Nerve, nerve root and plexus disorders
- (G50) Disorders of trigeminal nerve (V)
- (G51) Facial nerve disorders (VII)
- (G51.0) Bell’s palsy
- (G51.1) Geniculate ganglionitis
- (G51.2) Melkersson’s syndrome
- (G51.3) Clonic hemifacial spasm
- (G51.4) Facial myokymia
- (G51.8) Other disorders of facial nerve
- (G51.8) Disorder of facial nerve, unspecified
- (G52) Disorders of other cranial nerves
- (G52.0) Disorders of olfactory nerve (I)
- (G52.1) Disorders of glossopharyngeal nerve (IX)
- (G52.2) Disorders of vagus nerve (X)
- (G52.3) Disorders of hypoglossal nerve (XII)
- (G52.7) Disorders of multiple cranial nerves
- (G52.8) Disorders of other specified cranial nerves
- (G52.9) Cranial nerve disorder, unspecified
- (G53) Cranial nerve disorders in diseases classified elsewhere
- (G54) Nerve root and plexus disorders
- (G54.0) Brachial plexus disorders
- (G54.1) Lumbosacral plexus disorders
- (G54.2) Cervical root disorders, not elsewhere classified
- (G54.3) Thoracic root disorders, not elsewhere classified
- (G54.4) Lumbosacral root disorders, not elsewhere classified
- (G54.5) Neuralgic amyotrophy
- (G54.6) Phantom limb syndrome with pain
- (G54.7) Phantom limb syndrome without pain
- (G55) Nerve root and plexus compressions in diseases classified elsewhere
- (G56) Mononeuropathies of upper limb
- (G57) Mononeuropathies of lower limb
- (G57.0) Lesion of sciatic nerve
- (G57.1) Meralgia paraesthetica
- (G57.2) Lesion of femoral nerve
- (G57.3) Lesion of lateral popliteal nerve
- (G57.4) Lesion of medial popliteal nerve
- (G57.5) Tarsal tunnel syndrome
- (G57.6) Lesion of plantar nerve
- (G57.8) Other mononeuropathies of lower limb
- (G57.9) Mononeuropathy of lower limb, unspecified
- (G58) Other mononeuropathies
- (G58.0) Intercostal neuropathy
- (G58.7) Mononeuritis multiplex
- (G58.8) Other specified mononeuropathies
- (G58.9) Mononeuropathy, unspecified
- (G59) Mononeuropathy in diseases classified elsewhere
(G60-G64) Polyneuropathies and other disorders of the peripheral nervous system
- (G60) Hereditary and idiopathic neuropathy
- (G60.0) Hereditary motor and sensory neuropathy
- Charcot-Marie-Tooth disease
- Déjerine-Sottas disease
- Hereditary motor and sensory neuropathy, types I-IV
- Hypertrophic neuropathy of infancy
- Peroneal muscular atrophy (axonal type)(hypertrophic type)
- Roussy-Lévy syndrome
- (G60.1) Refsum’s disease
- (G60.2) Neuropathy in association with hereditary ataxia
- (G60.3) Idiopathic progressive neuropathy
- (G60.8) Other hereditary and idiopathic neuropathies
- (G60.9) Hereditary and idiopathic neuropathy, unspecified
- (G60.0) Hereditary motor and sensory neuropathy
- (G61) Inflammatory polyneuropathy
- (G61.0) Guillain-Barré syndrome
- (G61.1) Serum neuropathy
- (G61.8) Other inflammatory polyneuropathies
- (G61.9) Inflammatory polyneuropathy, unspecified
- (G62) Other polyneuropathies
- (G62.0) Drug-induced polyneuropathy
- (G62.1) Alcoholic polyneuropathy
- (G62.2) Polyneuropathy due to other toxic agents
- (G62.8) Other specified polyneuropathies
- (G62.9) Polyneuropathy, unspecified
- Neuropathy NOS
- (G63) Polyneuropathy in diseases classified elsewhere
- (G64) Other Disorders of peripheral nervous system
(G70-G73) Diseases of myoneural junction and muscle
- (G70) Myasthenia gravis and other myoneural disorders
- (G70.0) Myasthenia gravis
- (G70.1) Toxic myoneural disorders
- (G70.2) Congenital and developmental myasthenia
- (G71) Primary disorders of muscles
- (G71.0) Muscular dystrophy
- benign muscular dystrophy (Becker muscular dystrophy)
- benign scapuloperoneal muscular dystrophy with early contractures (Emery-Dreifuss muscular dystrophy)
- distal muscular dystrophy
- facioscapulohumeral muscular dystrophy
- limb-girdle muscular dystrophy
- ocular muscular dystrophy
- oculopharyngeal muscular dystrophy
- scapuloperoneal muscular dystrophy
- severe muscular dystrophy (Duchenne muscular dystrophy)
- (G71.1) Myotonic disorders
- Dystrophia myotonica (Steinert)
- chondrodystrophic myotonia
- drug-induced myotonia
- symptomatic myotonia
- Myotonia congenita – NOS:
- Myotonia congenita – dominant (Thomsen)
- Myotonia congenita – recessive (Becker)
- Neuromyotonia (Isaacs)
- Paramyotonia congenita
- Pseudomyotonia
- (G71.2) Congenital myopathies, including:
- (G71.3) Mitochondrial myopathy, not elsewhere classified
- (G71.0) Muscular dystrophy
- (G72) Other myopathies
- (G73) Disorders of myoneural junction and muscle in diseases classified elsewhere
- (G73.0) Myasthenic syndromes in endocrine diseases
- (G73.1) Eaton-Lambert syndrome
- (G73.2) Other myasthenic syndromes in neoplastic disease
- (G73.3) Myasthenic syndromes in other diseases classified elsewhere
- (G73.4) Myopathy in infectious and parasitic diseases classified elsewhere
- (G73.5) Myopathy in endocrine diseases
- (G73.6) Myopathy in metabolic diseases
- (G73.7) Myopathy in other diseases classified elsewhere
(G80-G83) Cerebral palsy and other paralytic syndromes
- (G80) Cerebral palsy
- (G80.0) Spastic quadriplegic cerebral palsy
- (G80.1) Spastic diplegic cerebral palsy
- (G80.2) Spastic hemiplegic cerebral palsy
- (G80.3) Dyskinetic cerebral palsy
- (G80.4) Ataxic cerebral palsy
- (G80.8) Other cerebral palsy
- (G80.9) Cerebral palsy, unspecified
- (G81) Hemiplegia
- (G81.0) Flaccid hemiplegia
- (G81.1) Spastic hemiplegia
- (G81.9) Hemiplegia, unspecified
- (G82) Paraplegia and tetraplegia
- (G82.0) Flaccid paraplegia
- (G82.1) Spastic paraplegia
- (G82.2) Paraplegia, unspecified
- Paralysis of both lower limbs NOS
- Paraplegia (lower) NOS
- (G82.3) Flaccid tetraplegia
- (G82.4) Spastic tetraplegia
- (G82.5) Tetraplegia, unspecified
- Quadriplegia NOS
- (G83) Other paralytic syndromes
- (G83.0) Diplegia of upper limbs
- (G83.1) Monoplegia of lower limb
- (G83.2) Monoplegia of upper limb
- (G83.3) Monoplegia, unspecified
- (G83.4) Cauda equina syndrome
- (G83.8) Other specified paralytic syndromes
- Todd’s paralysis (postepileptic)
- (G83.9) Paralytic syndrome, unspecified
(G90-G99) Other disorders of the nervous system
- (G90) Disorders of autonomic nervous system
- (G90.0) Idiopathic peripheral autonomic neuropathy
- (G90.1) Familial dysautonomia (Riley-Day)
- (G90.2) Horner’s syndrome
- (G90.3) Multi-system degeneration
- (G90.8) Other disorders of autonomic nervous system
- (G90.9) Disorder of autonomic nervous system, unspecified
- (G93) Other disorders of brain
- (G93.0) Cerebral cysts
- (G93.1) Anoxic brain damage, not elsewhere classified
- (G93.2) Benign intracranial hypertension
- (G93.3) Postviral fatigue syndrome
- (G93.4) Encephalopathy, unspecified
- (G93.5) Compression of brain
- (G93.6) Cerebral oedema
- (G93.7) Reye’s syndrome
- (G93.8) Other specified disorders of brain
- (G93.9) Disorder of brain, unspecified
- (G95) Other diseases of spinal cord
- (G95.0) Syringomyelia and syringobulbia
- (G95.1) Vascular myelopathies
- (G95.2) Cord compression, unspecified
- (G95.8) Other specified diseases of spinal cord
- (G95.9) Disease of spinal cord, unspecified
- Myelopathy NOS
- (G96) Other disorders of central nervous system
- (G97) Postprocedural disorders of nervous system, not elsewhere classified
- (G98) Other disorders of nervous system, not elsewhere classified
- (G99) Other disorders of nervous system in diseases classified elsewhere
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
The nervous system is a highly specialized network whose principal components are nerves called neurons. Neurons are interconnected to each other in complex arrangements, and have the property of conducting, using electrochemical signals, a great variety of stimuli both within the nervous tissue as well as from and towards most of the other tissues. Thus, neurons coordinate multiple functions in organisms. Nervous systems are found in many multicellular animals but differ greatly in complexity between species.

Nervous system in humans
The human nervous system can be observed both with gross anatomy, (which describes the parts that are large enough to be seen with the plain eye,) and microanatomy, (which describes the system at a cellular level.) At gross anatomy, the nervous system can be grouped in distinct organs, these being actually stations which the neural pathways cross through. Thus, with a didactical purpose, these organs, according to their ubication, can be divided in two parts: the central nervous system (CNS) and the peripheral nervous system (PNS).
Central nervous system
The central nervous system (CNS) represents the largest part of the nervous system, including the brain and the spinal cord. The CNS is contained within the dorsal cavity, with the brain within the cranial cavity, and the spinal cord in the spinal cavity. The CNS is covered by the meninges. The brain is also protected by the skull, and the spinal cord is also protected by the vertebrae. The nervous system can be connected into many systems that can function together. The two systems are central nervous system (CNS)and the peripheral nervous system (PNS).
Peripheral nervous system
The PNS consists of all the other nervous structures that do not lie within it. The large majority of what are commonly called nerves (which are actually axonal processes of nerve cells) are considered to be PNS.
Microanatomy
The nervous system is, on a small scale, primarily made up of neurons. However, glial cells also play a major role.
Neurons
They are the core components of both the central nervous system & peripheral nervous system. Neurons are sensors that send electric messages to the Central Nervous System which send the electric messages back to the neurons telling them how to react, where the messages are finally sent back directly to the brain. These messages travel at a usual pace of 100 meters per second.
Glial cells
Glial cells are non-neuronal cells that provide support and nutrition, maintain homeostasis, form myelin, and participate in signal transmission in the nervous system. In the human brain, glia are estimated to outnumber neurons by about 10 to 1.[1]
Glial cells provide support and protection for neurons. They are thus known as the “glue” of the nervous system. The four main functions of glial cells are to surround neurons and hold them in place, to supply nutrients and oxygen to neurons, to insulate one neuron from another, and to destroy pathogens and remove dead neurons.
Physiological division
A less anatomical but much more functional division of the human nervous system is that classifying it according to the role that the different neural pathways play, regardless whether these cross through the CNS or the PNS:
The somatic nervous system is responsible for coordinating the body’s movements, and also for receiving external stimuli. It is the system that regulates activities that are under conscious control.
The autonomic nervous system is then split into the sympathetic division, parasympathetic division, and enteric division. The sympathetic nervous system responds to impending danger or stress, and is responsible for the increase of one’s heartbeat and blood pressure, among other physiological changes, along with the sense of excitement one feels due to the increase of adrenaline in the system. The parasympathetic nervous system, on the other hand, is evident when a person is resting and feels relaxed, and is responsible for such things as the constriction of the pupil, the slowing of the heart, the dilation of the blood vessels, and the stimulation of the digestive and genitourinary systems. The role of the enteric nervous system is to manage every aspect of digestion, from the esophagus to the stomach, small intestine and colon.
In turn, these pathways can be divided according to the direction in which they conduct stimuli:
- Afferent system by sensory neurons, which carry impulses from a receptor to the CNS
- Efferent system by motor neurons, which carry impulses from the CNS to an effector
- Relay system by relay neurons (also called interneurons), which transmit impulses between the sensory and motor neurones.
A useful mnemonic to remember the nature of Afferent vs Efferent is SAME DAVE: Sensory Afferent, Motor Efferent; Dorsal Afferent, Ventral Efferent
However, there are relay neurons in the CNS as well.
The junction between two neurones is called a synapse. There is a very narrow gap (about 20nm in width) between the neurons – the synaptic cleft, where an action potential is transmitted from one neuron to a neighboring one. They do this by relaying the message with the use of neurotransmitters which the next neuron then receives the electrical signal, known as a nerve impulse. The nerve impulse is determined by the neurotransmitter to then carry the message to its appropriate destination. These nerve impulses are a change in ion balance in the nerve cell, which the central nervous system can then interpret. The fact that the nervous system uses a mixture of electrical and chemical signals makes it incredibly fast, which is necessary to acknowledge the presence of danger. For example, a hand touching a hot stove. If the nervous system was only comprised of chemical signals, the body would not tell the arm to move fast enough to escape dangerous burns. So the speed of the nervous system is a necessity for life.
| Physiological division | Somatic nervous system | Afferent system | ||
| Efferent system | ||||
| Autonomic nervous system | Sympathetic | Afferent system | ||
| Efferent system | ||||
| Parasympathetic | Afferent system | |||
| Efferent system | ||||
Development
Some landmarks of embryonic neural development include the birth and differentiation of neurons from stem cell precursors, the migration of immature neurons from their birthplaces in the embryo to their final positions, outgrowth of axons from neurons and guidance of the motile growth cone through the embryo towards postsynaptic partners, the generation of synapses between these axons and their postsynaptic partners, and finally the lifelong changes in synapses which are thought to underlie learning and memory.
Importance
Many people have lost basic motor skills and other skills because of spinal chord injuries. If this portion is damaged, the biggest nerve and the most important one gets damaged. This leads to paralysis or other permanent damages.
Abilities
The nervous system is able to make basic motor skills and other skills possible. The basic 5 senses of texture, taste, sight, smell,and hearing are powered by the nervous system. If disabled, basic motor skills may be lost.
Non-humans
Vertebrates
The nervous system of all vertebrate animals, is often divided into the central nervous system (CNS) and the peripheral nervous system (PNS). The CNS consists of the brain and spinal cord.
Worms
Planaria, a type of flatworm, have dual nerve cords running along the length of the body and merging at the tail and the mouth. These nerve cords are connected by transverse nerves like the rungs of a ladder. These transverse nerves help coordinate the two sides of the animal. Two large ganglia at the head end function similar to a simple brain. Photoreceptors on the animal’s eyespots provide sensory information on light and dark.
The nervous system of the roundworm Caenorhabditis elegans has been mapped out to the cellular level. Every neuron and its cellular lineage has been recorded and most, if not all, of the neural connections are known. In this species, the nervous system is sexually dimorphic; the nervous systems of the two sexes, males and hermaphrodites, have different numbers of neurons and groups of neurons that perform sex-specific functions. In C. elegans, males have exactly 383 neurons, while hermaphrodites have exactly 302 neurons [2]
Arthropoda
Arthropods, such as insects and crustaceans, have a nervous system made up of a series of ganglia, connected by a ventral nerve cord made up of two parallel connectives running along the length of the belly [3]. Typically, each body segment has one ganglion on each side, though some ganglia are fused to form the brain and other large ganglia [4].
The head segment contains the brain, also known as the supraesophageal ganglion. In the insect nervous system, the brain is anatomically divided into the protocerebrum, deutocerebrum, and tritocerebrum. Immediately behind the brain is the subesophageal ganglion, which is composed of three pairs of fused ganglia. It controls the mouthparts, the salivary glands and certain muscles.
Many arthropods have well-developed sensory organs, including compound eyes for vision and antennae for olfaction and pheromone sensation. The sensory information from these organs is processed by the brain.
Development
Neural development in most species have many similarities neural development in humans.
External links
- Neuroscience for Kids
- The Human Brain Project Homepage
- Kimball’s Biology Pages, CNS
- Kimball’s Biology Pages, PNS
Template:Organ systems Template:Nervous system Template:Somatosensory system
Template:Nervous system physiology Template:Diseases of the nervous system Template:Development of nervous system Template:Neurosurgical procedures
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See also
See also
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
Template:CNS diseases of the nervous system Template:PNS diseases of the nervous system Template:Cerebral palsy and other paralytic syndromes
hu:BNO-10-06 – Az idegrendszer betegségei nl:ICD10 Hoofdstuk VI te:ICD-10 అధ్యాయము 6: నాడీ వ్యవస్థకు సంబంధించిన వ్యాధులు th:ICD-10 บท G: โรคระบบประสาท Template:WH Template:WS Template:Jb1
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