ICD-10 บท G: โรคระบบประสาท

จากวิกิพีเดีย สารานุกรมเสรี

เนื้อหา 1 G00-G99 - โรค ระบบประสาท 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 ดูเพิ่ม

[แก้] G00-G99 - โรค ระบบประสาท

[แก้] (G00-G09) Inflammatory diseases of the central nervous system

• (G00.) Bacterial meningitis, not elsewhere classified
• (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
• (G04.) Encephalitis, myelitis and encephalomyelitis
  • (G04.0) Acute disseminated encephalitis
• (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

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

• (G10.) Huntington's disease
• (G11.) Hereditary ataxia
  • (G11.1) Early-onset cerebellar ataxia
    • Friedreich's ataxia (autosomal recessive)
  • (G11.2) Late-onset cerebellar ataxia
  • (G11.3) Cerebellar ataxia with defective DNA repair
    • Ataxia telangiectasia (Louis-Bar)
  • (G11.4) Hereditary spastic paraplegia
• (G12.) Spinal muscular atrophy and related syndromes
  • (G12.0) Werdnig-Hoffman disease (Type 1)
  • (G12.1) Other inherited spinal muscular atrophy
    • Kugelberg-Welander disease (Type 3)
  • (G12.2) Motor neuron disease
• (G13.) Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere

[แก้] (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
• (G24.) Dystonia
  • (G24.5) Blepharospasm
• (G25.) Other extrapyramidal and movement disorders
  • (G25.0) Essential tremor
  • (G25.3) Myoclonus
• (G26.) Extrapyramidal and movement disorders in diseases classified elsewhere

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

• (G30.) Alzheimer's disease
• (G31.) Other degenerative diseases of nervous system, not elsewhere classified
• (G32.) Other degenerative disorders of nervous system in diseases classified elsewhere

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

• (G35.) Multiple sclerosis
• (G36.) Other acute disseminated demyelination
• (G37.) Other demyelinating diseases of central nervous system
  • (G37.2) Central pontine myelinolysis

[แก้] (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 (Kozhevnikof)
  • (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

• (G43.) Migraine
  • (G43.0) Migraine without aura (common migraine)
  • (G43.1) Migraine with aura (classical migraine)
  • (G43.2) Status migrainosus
  • (G43.3) Complicated migraine
  • (G43.4) Other migraine
  • (G43.5) 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
  • (G45.3) Amaurosis fugax
• (G46.) 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

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

• (G50.) Disorders of trigeminal nerve
  • (G50.0) Trigeminal neuralgia
• (G51.) Facial nerve disorders
  • (G51.0) Bell's palsy
• (G52.) Disorders of other cranial nerves
• (G53.) Cranial nerve disorders in diseases classified elsewhere
• (G54.) Nerve root and plexus disorders
  • (G54.0) Brachial plexus disorders
    • Thoracic outlet 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
  • (G57.5) Tarsal tunnel syndrome
• (G58.) Other mononeuropathies
• (G59.) Mononeuropathy in diseases classified elsewhere

[แก้] (G60-G64) Polyneuropathies and other disorders of the peripheral nervous system

• (G60.) Hereditary and idiopathic neuropathy
• (G61.) Inflammatory polyneuropathy
  • (G61.0) Guillain-Barré syndrome
• (G62.) Other polyneuropathies
  • (G62.1) Alcoholic polyneuropathy
• (G63.) Polyneuropathy in diseases classified elsewhere
• (G64.) Other Disorders of peripheral nervous system

[แก้] (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
    • Becker's muscular dystrophy
    • Duchenne muscular dystrophy
    • Facioscapulohumeral dystrophy
    • Fukuyama congenital muscular dystrophy (FCMD)
    • Limb-girdle muscular dystrophy
    • Myotonic muscular dystrophy
    • Oculopharyngeal muscular dystrophy
  • (G71.1) Myotonic disorders
  • (G71.2) Congenital myopathies
  • (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

[แก้] (G80-G83) Cerebral palsy and other paralytic syndromes

• (G80.) Infantile cerebral palsy
• (G81.) Hemiplegia
• (G82.) Paraplegia and tetraplegia
• (G83.) Other paralytic syndromes
  • (G83.4) Cauda equina syndrome

[แก้] (G90-G99) Other disorders of the nervous system

• (G90.) Disorders of autonomic nervous system
  • (G90.2) Horner's syndrome
• (G91.) Hydrocephalus
• (G92.) Toxic encephalopathy
• (G93.) Other disorders of brain
  • (G93.2) Benign intracranial hypertension
  • (G93.3) Postviral fatigue syndrome
  • (G93.6) Cerebral oedema
  • (G93.7) Reye's syndrome
• (G94.) Other disorders of brain in diseases classified elsewhere
• (G95.) Other diseases of spinal cord
• (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

[แก้] ดูเพิ่ม

• รายการอาการในรหัส ICD-10 (List of ICD-10 codes)
• การจำแนกประเภทของโรคตามสถิติและปัญหาสาธารณะสุขสัมพันธ์ระหว่างประเทศ (International Statistical Classification of Diseases and Related Health Problems)

ICD-10 บท G: โรคระบบประสาท เป็นบทความเกี่ยวกับ การแพทย์  ที่ยังไม่สมบูรณ์ ต้องการตรวจสอบ เพิ่มเนื้อหา หรือเพิ่มแหล่งอ้างอิง คุณสามารถช่วยเพิ่มเติมหรือแก้ไข เพื่อให้สมบูรณ์มากขึ้น ข้อมูลเกี่ยวกับ ICD-10 บท G: โรคระบบประสาท ในภาษาอื่น อาจสามารถหาอ่านได้จากเมนู ภาษาอื่น ด้านซ้ายมือ