Category:Neurological disorders
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 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes G00-G99 should be included in this category. |
 | Pages in this category should be moved to subcategories where applicable. This category may require frequent maintenance to avoid becoming too large. It should directly contain very few, if any, pages and should mainly contain subcategories. |
This category encompasses all disorders of the nervous system. The major meta-categories is Category:Neurological disorders by disease category. A disorder can be categorized in both systems simultaneously (for example, glioma under "Nervous system neoplasia" AND "Brain disorders").
Please sort articles into these sub-categories and avoid categorizing them simply with the parent category Neurological disorders.
If an article is about a symptom or finding on neurologic examination (for example, alexia without agraphia), please sort it into Category:Symptoms and signs: Nervous system.
Subcategories
This category has the following 7 subcategories, out of 7 total.
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Pages in category "Neurological disorders"
The following 200 pages are in this category, out of 1,262 total.
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- Abdallat–Davis–Farrage syndrome
- Abdominal epilepsy
- Abetalipoproteinemia
- Ablative brain surgery
- Absent-mindedness
- Abulia
- Acalculia
- Acalvaria
- Accessory nerve disorder
- Acephalgic migraine
- Aceruloplasminemia
- Achalasia microcephaly
- Achiria
- Acute motor axonal neuropathy
- Adaptive deep brain stimulation
- Adie
- Adie syndrome
- ADNP syndrome
- Adrenoleukodystrophy
- Adult polyglucosan body disease
- Afu
- Agnosia
- Agraphesthesia
- Agraphia
- Aicardi
- Aicardi syndrome
- Aicardi–Goutières syndrome
- Akinetic mutism
- Akinetopsia
- Alcohol-related dementia
- Alcoholic polyneuropathy
- Alice
- Alien hand syndrome
- Allodynia
- ALS
- ALS Association
- ALS2
- Alternating hemiplegia
- Alternating hemiplegia of childhood
- Alzheimer Disease and Associated Disorders
- Alzheimer's disease
- Amaurosis
- Amnesia
- Amnesic shellfish poisoning
- Amorphosynthesis
- Amyotrophic lateral sclerosis research
- Anaphia
- Anarthria
- Andermann syndrome
- Anesthesia dolorosa
- Aneurysm
- Angelman syndrome
- Angiolathyrism
- Anomic aphasia
- Anopsia
- Anosodiaphoria
- Anoxia
- Anterior cutaneous nerve entrapment syndrome
- Anterior horn disease
- Anterior interosseous syndrome
- Anterior ischemic optic neuropathy
- Anti-AQP4 disease
- Anti-IgLON5 disease
- Anti-neurofascin demyelinating diseases
- Antiganglioside antibodies
- Antiphospholipid syndrome
- Anton syndrome
- Ape hand deformity
- Aphantasia
- Apolipoprotein E
- Apperceptive agnosia
- Apraxia
- Apraxia of speech
- Aprosodia
- Aquadynia
- Arachnoid cyst
- Intracranial cysts
- Araf
- Arakawa's syndrome II
- Argentine tea culture
- Argonaute
- Aromatic L-amino acid decarboxylase deficiency
- Arts syndrome
- Arylsulfatase A
- ASD
- Aspartylglucosaminuria
- Asperger syndrome
- Astasis
- Asterixis
- Ataxia
- Ataxia with vitamin E deficiency
- Ataxia-pancytopenia syndrome
- Ataxia–telangiectasia
- Ataxic cerebral palsy
- Ataxic respiration
- Athetoid cerebral palsy
- Athetosis
- Athymhormia
- Atlanto-occipital dislocation
- Atonic seizure
- ATP13A2
- ATP1A2
- ATPAF2
- ATR-X syndrome
- Atypical trigeminal neuralgia
- Auditory agnosia
- Auh
- Aura (symptom)
- Autoimmune autonomic ganglionopathy
- Autoimmune optic neuropathy
- Autonomic neuropathy
- Autosomal dominant cerebellar ataxia
- Autosomal dominant GTP cyclohydrolase I deficiency
- Autosomal dominant porencephaly type I
- Autosomal recessive cerebellar ataxia type 1
- Autosomal recessive spastic ataxia of Charlevoix-Saguenay
- Autotopagnosia
- Avellis syndrome
- AVM
- Axillary nerve dysfunction
- Axillary nerve palsy
B
- Balance disorder
- Balo concentric sclerosis
- Basal ganglia disease
- Basilar invagination
- Batten
- Behr syndrome
- Belper Hirn
- Benedikt syndrome
- Benign familial infantile epilepsy
- Benign familial neonatal seizures
- Benign fasciculation syndrome
- Benign infantile epilepsy
- Benign paroxysmal torticollis
- Benign paroxysmal vertigo of childhood
- Berm
- BICD2
- Bickerstaff brainstem encephalitis
- Bignami
- Bilateral frontoparietal polymicrogyria
- Binasal hemianopsia
- Binswanger's disease
- Black out
- Bladder sphincter dyssynergia
- Blocq's disease
- Bobath concept
- Bok
- Borna disease
- Bosch–Boonstra–Schaaf optic atrophy syndrome
- Brachial plexus injury
- Bradyesthesia
- Brain damage
- Brain fever
- Brain stem tumor
- Brain-lung-thyroid syndrome
- Brainstem stroke syndrome
- Breath-holding spell
- Brewer infarcts
- Bromism
- Brown-Séquard syndrome
- Riboflavin transporter deficiency
- Brown–Vialetto–Van Laere syndrome
- Bruns apraxia
- Bulbar palsy
- Burning mouth syndrome
- Bálint
- Bálint's syndrome
C
- CAA
- CACNG1
- Calloso genital dysplasia
- Camel spongiform encephalopathy
- Camptocormia
- Candidate
- CARASIL
- Carpal spasm
- Carpal tunnel
- Carphologia
- Cataplexy
- Cauda equina syndrome
- Caudal pontine reticular nucleus
- Causes and origins of Tourette syndrome
- Causes of Parkinson's disease
- CCM
- CDKL5 deficiency disorder
- CEDNIK syndrome
- Celeste Imperio
- Cennamo–Gangemi syndrome
- Central chromatolysis
- Central facial palsy
- Central hypoventilation syndrome
- Central nervous system cyst
- Central nervous system tumor
- Central neurogenic hyperventilation
- Cephalic disorder
- Cerebellar agenesis
