ICD-10 Chapter VI: Diseases of the nervous system

From Wikipedia, the free encyclopedia

Contents 1 G00-G99 - Diseases of the nervous system 1.1 (G00-G09) Inflammatory diseases of the central nervous system 1.2 (G10-G13) Systemic atrophies primarily affecting the central nervous system 1.3 (G20-G26) Extrapyramidal and movement disorders 1.4 (G30-G32) Other degenerative diseases of the nervous system 1.5 (G35-G37) Demyelinating diseases of the central nervous system 1.6 (G40-G47) Episodic and paroxysmal disorders 1.7 (G50-G59) Nerve, nerve root and plexus disorders 1.8 (G60-G64) Polyneuropathies and other disorders of the peripheral nervous system 1.9 (G70-G73) Diseases of myoneural junction and muscle 1.10 (G80-G83) Cerebral palsy and other paralytic syndromes 1.11 (G90-G99) Other disorders of the nervous system 2 See also

[edit] G00-G99 - Diseases of the nervous system

[edit] (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

[edit] (G10-G13) Systemic atrophies primarily affecting the central nervous system

• (G10.) Huntington's disease

• (G11.) Hereditary ataxia
  • (G11.0) Congenital nonprogressive ataxia
  • (G11.1) Early-onset cerebellar ataxia
    • Early-onset cerebellar ataxia with essential tremor
    • Early-onset cerebellar ataxia with myoclonus (Hunt's ataxia)
    • Early-onset cerebellar ataxia with retained tendon reflexes
    • Friedreich's ataxia (autosomal recessive)
    • X-linked recessive spinocerebellar 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
    • Progressive bulbar palsy of childhood (Fazio-Londe)
    • Kugelberg-Welander disease (Type 3)
  • (G12.2) Motor neuron disease
    • Familial motor neuron disease
    • Amyotrophic lateral sclerosis
    • Primary lateral sclerosis
    • Progressive bulbar palsy
    • Progressive spinal muscular atrophy

• (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
    • Paraneoplastic limbic encephalopathy
  • (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

[edit] (G20-G26) Extrapyramidal and movement disorders

• (G20.) Parkinson's disease

• (G21.) Secondary parkinsonism
  • (G21.0) Malignant neuroleptic syndrome
  • (G21.3) Postencephalitic parkinsonism

• (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

• (G24.) Dystonia
  • (G24.0) Drug-induced dystonia
  • (G24.1) Idiopathic familial dystonia
  • (G24.2) Idiopathic nonfamilial dystonia
  • (G24.3) Spasmodic torticollis
  • (G24.4) Idiopathic orofacial dystonia
    • Orofacial dyskinesia
  • (G24.5) Blepharospasm
  • (G24.8) Other dystonia
  • (G24.9) Dystonia, unspecified
    • Dyskinesia NOS

• (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
    • Restless legs syndrome
    • Stiff-man syndrome
  • (G25.9) Extrapyramidal and movement disorder, unspecified

• (G26.) Extrapyramidal and movement disorders in diseases classified elsewhere

[edit] (G30-G32) Other degenerative diseases of the nervous system

• (G30.) Alzheimer's disease

• (G31.) Other degenerative diseases of nervous system, not elsewhere classified
  • (G31.0) Circumscribed brain atrophy
    • Pick's disease
  • (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
    • Grey-matter degeneration (Alpers)
    • Lewy body dementia
    • Subacute necrotizing encephalopathy (Leigh)
  • (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

[edit] (G35-G37) Demyelinating diseases of the central nervous system

• (G35.) Multiple sclerosis

• (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

[edit] (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:
      • atonic
      • clonic
      • myoclonic
      • tonic
      • tonic-clonic
  • (G40.4) Other generalized epilepsy and epileptic syndromes
    • Epilepsy with:
      • myoclonic absences
      • myoclonic-astatic seizures
    • Infantile spasms
    • Lennox-Gastaut syndrome
    • Salaam attacks
    • Symptomatic early myoclonic encephalopathy
    • West's syndrome
  • (G40.5) Special epileptic syndromes
    • Epilepsia partialis continua (Kozhevnikov)
  • (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) Vertebrobasilar 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
    • Benedikt syndrome
    • Claude syndrome
    • Foville syndrome
    • Millard-Gubler syndrome
    • Wallenberg syndrome
    • Weber 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

[edit] (G50-G59) Nerve, nerve root and plexus disorders

• (G50.) Disorders of trigeminal nerve (V)
  • (G50.0) Trigeminal neuralgia

• (G51.) Facial nerve disorders (VII)
  • (G51.0) Bell's palsy
    • Facial palsy
  • (G51.1) Geniculate ganglionitis
  • (G51.2) Melkersson's syndrome
    • Melkersson-Rosenthal 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
    • Thoracic outlet syndrome
  • (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
    • Parsonage-Aldren-Turner syndrome
  • (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
  • (G56.0) Carpal tunnel syndrome
  • (G56.4) Causalgia
• (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
    • Morton's metatarsalgia
  • (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

[edit] (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
    • Morvan's disease
    • Nelaton's syndrome
    • Sensory neuropathy
  • (G60.9) Hereditary and idiopathic neuropathy, unspecified

• (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

[edit] (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:
    • Central core disease
    • Congenital muscular dystrophy
    • Centronuclear myopathy
    • Fibre-type disproportion
    • Minicore disease
    • Multicore disease
    • Myotubular myopathy
    • Nemaline myopathy
  • (G71.3) Mitochondrial myopathy, not elsewhere classified
• (G72.) Other myopathies
  • (G72.0) Drug-induced myopathy
  • (G72.1) Alcoholic myopathy
  • (G72.2) Myopathy due to other toxic agents
  • (G72.3) Periodic paralysis
    • Hypokalemic periodic paralysis
    • Hyperkalemic periodic paralysis
• (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

[edit] (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

[edit] (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

• (G91.) Hydrocephalus
• (G92.) Toxic encephalopathy

• (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
    • Postradiation encephalopathy
  • (G93.9) Disorder of brain, unspecified

• (G94.) Other disorders of brain in diseases classified elsewhere

• (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
  • (G96.0) Cerebrospinal fluid leak
  • (G96.1) Disorders of meninges, not elsewhere classified
    • Meningeal adhesions (cerebral)(spinal)
  • (G96.8) Other specified disorders of central nervous system
  • (G96.9) Disorder of central nervous system, unspecified

• (G97.) Postprocedural disorders of nervous system, not elsewhere classified
  • (G97.0) Cerebrospinal fluid leak from spinal puncture
  • (G97.1) Other reaction to spinal and lumbar puncture
  • (G97.2) Intracranial hypotension following ventricular shunting
  • (G97.8) Other postprocedural disorders of nervous system
  • (G97.9) Postprocedural disorder of nervous system, unspecified

• (G98.) Other disorders of nervous system, not elsewhere classified

• (G99.) Other disorders of nervous system in diseases classified elsewhere

[edit] See also

• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems

v • d • e Pathology: Medical conditions (Diseases/Disorders/Illness, Syndromes/Sequences, Symptoms/Signs, Injuries, etc.) (A/B, 001-139) Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease (Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis (C/D, 140-239 & 280-289) Cancer (C00-D48, 140-239) Tumor Myeloid hematologic (D50-D77, 280-289) Anemia · Coagulopathy Lymphoid immune (D80-D89, 279) Immunodeficiency · Immunoproliferative disorder · Hypersensitivity (E, 240-278) Endocrine disease · Nutrition disorder · Inborn error of metabolism (F, 290-319) Mental disorder (G, 320-359) Nervous system disease (CNS, PNS) · Neuromuscular disease (H, 360-389) Eye disease · Ear disease (I, 390-459) Cardiovascular disease (Heart disease, Vascular disease) (J, 460-519) Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia) (K, 520-579) Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach, Enteropathy, Liver, Pancreatic) (L, 680-709) Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease) (M, 710-739) Musculoskeletal disorders · Osteochondropathy (Osteopathy, Chondropathy) (N, 580-629) Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast disease · Female genital disease (O, 630-679) Complications of pregnancy (P, 760-779) Fetal disease (Q, 740-759) Congenital disorder (R, 780-799) Syndromes · Medical signs (Eponymous) (S/T, 800-999) Bone fracture · Dislocations/subluxation · Sprain · Strain · Head injury · Chest trauma · Poisoning

v • d • e Pathology of the nervous system, primarily CNS (G00–G47, 320–349) Brain/ encephalopathy Inflammatory Encephalitis (Viral encephalitis, Herpesviral encephalitis) · Cavernous sinus thrombosis · Brain abscess (Amoebic) Degenerative Extrapyramidal and movement disorders Basal ganglia disease: Parkinsonism (Parkinson's disease, Postencephalitic parkinsonism)  · Neuroleptic malignant syndrome  · Pantothenate kinase-associated neurodegeneration · Progressive supranuclear palsy · Striatonigral degeneration · Hemiballismus · Huntington's disease · Olivopontocerebellar atrophy Dyskinesia: Dystonia (Spasmodic torticollis, Meige's, Blepharospasm) · Chorea (Choreoathetosis)  · Myoclonus (Myoclonic epilepsy) Essential tremor  · Restless legs  · Stiff person Dementia Alzheimer's (Early-onset)  · Frontotemporal dementia/Frontotemporal lobar degeneration (Pick's, Dementia with Lewy bodies) · Multi-infarct dementia Mitochondrial disease Leigh's Demyelinating autoimmune (Multiple sclerosis, Neuromyelitis optica, Schilder's disease) · hereditary (Adrenoleukodystrophy, Alexander, Canavan, Krabbe, ML, Pelizaeus-Merzbacher, VWM, MFC, CAMFAK syndrome) · Central pontine myelinolysis · Marchiafava-Bignami disease  · Alpers' Episodic/ paroxysmal Seizure/epilepsy Focal  · Generalised  · Status epilepticus  · Myoclonic epilepsy Headache Migraine (Familial hemiplegic)  · Cluster  · Vascular  · Tension Vascular Transient ischemic attack (Amaurosis fugax, Transient global amnesia) Cerebrovascular disease  · Stroke (MCA, ACA, PCA, Foville's, Millard-Gubler, Lateral medullary, Weber's, Lacunar stroke) Sleep disorders Insomnia  · Hypersomnia  · Sleep apnea (Obstructive, Ondine's curse)  · Narcolepsy  · Cataplexy  · Kleine-Levin  · Circadian rhythm sleep  · Delayed sleep phase  · Advanced sleep phase CSF Intracranial hypertension (Hydrocephalus/Normal pressure, Idiopathic intracranial hypertension) · Cerebral edema · Intracranial hypotension Other Brain herniation · Reye's  · Hepatic encephalopathy  · Toxic encephalopathy Spinal cord/ myelopathy Inflammatory Myelitis: Poliomyelitis · Demyelinating disease (Transverse myelitis) · Tropical spastic paraparesis Other Syringomyelia · Syringobulbia · Morvan's syndrome · Vascular myelopathy (Foix-Alajouanine syndrome) · Spinal cord compression Both/either Inflammatory Encephalomyelitis (Acute disseminated) Meningitis/Arachnoiditis: Bacterial (Tuberculous, Haemophilus, Pneumococcal) · Viral (Herpesviral) · Fungal (Cryptococcal) · Aseptic (Drug-induced) Meningoencephalitis Systemic atrophies SA Friedreich's ataxia · Ataxia telangiectasia MND UMN only: PLS · PP · HSP LMN only: PMA · PBP (Fazio-Londe, Infantile progressive bulbar palsy) · SMA (SMN-linked, Kennedy disease, SMAX2, DSMA1) both: ALS see also congenital, tumors

v • d • e Nervous system pathology, PNS (G50-G64, 350-357) Somatic Nerve, nerve root, plexus Cranial nerve disease V (Trigeminal neuralgia) · VII (Facial nerve paralysis, Bell's palsy, Melkersson-Rosenthal syndrome, Central seven) · XI (Accessory nerve disorder) Radiculopathy, plexopathy brachial plexus (Brachial plexus lesion, Thoracic outlet syndrome) · Phantom limb Mono- neuropathy Upper limb median nerve (Carpal tunnel syndrome) ulnar nerve (Ulnar nerve entrapment, Froment's sign, Guyon's canal syndrome, Ulnar claw) radial nerve (Radial neuropathy, Wrist drop) long thoracic nerve (Winged scapula) Lower limb lateral cutaneous nerve of thigh (Meralgia paraesthetica) · tibial nerve (Tarsal tunnel syndrome) · plantar nerve (Morton's neuroma) superior gluteal nerve (Trendelenburg's sign) General Causalgia · Mononeuritis multiplex Polyneuropathies/ Polyradiculoneuropathy HMSN Charcot-Marie-Tooth disease · Dejerine Sottas syndrome · Refsum's disease · Hereditary spastic paraplegia Autoimmune/demyelinating Guillain-Barré syndrome · Chronic inflammatory demyelinating polyneuropathy Other Alcoholic polyneuropathy Dysautonomia, autonomic- neuropathy HSAN (I, II, III/Familial dysautonomia, IV/Congenital insensitivity to pain with anhidrosis, V) · Horner's syndrome · Multiple system atrophy

v • d • e Diseases of myoneural junction and muscle / neuromuscular disease (G70-G73, 358-359) Neuromuscular- junction disease autoimmune (Myasthenia gravis, Lambert-Eaton myasthenic syndrome) Myopathy Muscular dystrophy (DAPC) AD Limb-girdle muscular dystrophy 1 · Oculopharyngeal · Facioscapulohumeral · Myotonic · Distal (most) AR Limb-girdle muscular dystrophy 2 · Congenital (Fukuyama, Ullrich) XR dystrophin (Becker's, Duchenne) · Emerin Emery-Dreifuss Channelopathy Myotonia Myotonia congenita · Thomsen disease · Neuromyotonia/Isaacs syndrome · Paramyotonia congenita Periodic paralysis Hypokalemic · Hyperkalemic Congenital myopathy Bethlem myopathy · Central core disease · Centronuclear myopathy · Nemaline myopathy · Zaspopathy Mitochondrial myopathy MELAS · MERRF · KSS · PEO Other Inflammatory myopathy

v • d • e Cerebral palsy and other paralytic syndromes (G80-G83, 342-344) Paresis and plegia NOS Paralysis - Quadriplegia - Triplegia - Hemiplegia/Hemiparesis - Paraplegia/Diplegia - Monoplegia Flaccid vs. spastic Upper motor neuron lesion: Spastic diplegia - Spastic paraplegia (Hereditary spastic paraplegia) Lower motor neuron lesion: Flaccid paralysis Specific types Cerebral palsy - Cauda equina syndrome - Locked-in syndrome