Category:Neurological disorders
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 within Chapter VI: Diseases of the nervous system 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 8 subcategories, out of 14 total.
(previous page) (next page)Pages in category "Neurological disorders"
The following 200 pages are in this category, out of approximately 329 total. This list may not reflect recent changes.
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H
- Heavy legs
- Hemimegalencephaly
- Hemimotor neglect
- Hereditary cystatin C amyloid angiopathy
- Hereditary hemorrhagic telangiectasia
- Hereditary motor and sensory neuropathy
- Hereditary neuralgic amyotrophy
- Hereditary neuropathy with liability to pressure palsy
- Holmes tremor
- Hopkins syndrome
- Hyperekplexia
- Hyperkinesia
- Hypokalemic sensory overstimulation
- Hypsarrhythmia
I
- Ideational apraxia
- Ideomotor apraxia
- Impact of the COVID-19 pandemic on neurological, psychological and other mental health outcomes
- Infantile convulsions and choreoathetosis
- Integrative agnosia
- Intention tremor
- Intracranial hypertension syndrome
- Involuntary crying
- Involuntary emotional expression disorder
- Involuntary laughter
- Ischemic monomelic neuropathy
L
M
- Macropsia
- Management of multiple sclerosis
- Manganism
- Marche à petit pas
- McDonald criteria
- Meralgia paraesthetica
- Mevalonate kinase deficiency
- Microphthalmia, syndromic 12 (MCOPS12)
- Micropsia
- Migraine-associated vertigo
- Migralepsy
- Moebius syndrome
- Motion sickness
- Motor disorder
- Motor speech disorders
- Movement disorder
- Muenke syndrome
- Multifocal motor neuropathy
- Muscle fatigue
- Muscle weakness
- Myalgic encephalomyelitis/chronic fatigue syndrome
N
- Neuralgia
- Neurasthenia
- Neurodegenerative disease
- Neurodevelopmental disorder
- Neuroferritinopathy
- Neurofibromatosis type I
- Neurofibromatosis type II
- Neurogenic shock
- Neuroglycopenia
- Neurological deficit
- Neuroma
- Neuromodulation (medicine)
- Neuronal migration disorder
- Neuropsychiatric systemic lupus erythematosus
- Neurosarcoidosis
- Neurotoxicity
- NIH Toolbox
- Norman–Roberts syndrome
- Notalgia paresthetica
- Nystagmus
O
P
- Paradoxical embolism
- Paragraphia
- Paresthesia
- Parkinson-plus syndrome
- Paroxysmal attack
- Paroxysmal dyskinesia
- Paroxysmal exercise-induced dystonia
- Paroxysmal extreme pain disorder
- Paroxysmal kinesigenic choreoathetosis
- Paroxysmal nonkinesigenic dyskinesia
- Peduncular hallucinosis
- Perisylvian syndrome
- Peroneal nerve paralysis
- Phantom eye syndrome
- Phantom limb
- Phantosmia
- Phonagnosia
- Phonological dyslexia
- Photophobia
- Pleurothotonus
- Pneumocephalus
- POEMS syndrome
- Poser criteria
- Post-chemotherapy cognitive impairment
- Postherpetic neuralgia
- Postperfusion syndrome
- Preherpetic neuralgia
- Progressive inflammatory neuropathy
- Protein aggregation
- Proteinopathy
- PRRT2
- Psychoorganic syndrome
- Pusher syndrome
R
- Rabbit syndrome
- Rabies
- Radial nerve dysfunction
- Radiologically isolated syndrome
- Rage syndrome
- Ramsay Hunt syndrome
- Ramsay Hunt syndrome type 1
- Ramsay Hunt syndrome type 3
- Ramsay Hunt syndrome type 2
- Raymond–Céstan syndrome
- Recurrent painful ophthalmoplegic neuropathy
- Retinal migraine
- Revesz syndrome
- Rhythmic movement disorder
- Rich focus
S
- Scanning speech
- Schumacher criteria
- Scintillating scotoma
- Sensory neuronopathy
- Sensory processing disorder
- Sensory Processing Disorder Foundation
- Shapiro syndrome
- Simulated presence therapy
- SLC13A5 citrate transporter disorder
- Social-emotional agnosia
- Sopite syndrome
- Spasmodic torticollis
- Spastic diplegia
- Spastic quadriplegia
- Spinal muscular atrophies
- Spinocerebellar ataxia type 6
- Stereotypic movement disorder
- Strephosymbolia
- Subacute myelo-optic neuropathy
- Subclavian steal syndrome
- Subdural effusion
- Subdural hygroma
- Subgaleal hemorrhage
- Suboccipital puncture
- Supernumerary phantom limb
- Surfer's myelopathy
- Susac's syndrome
- Sydenham's chorea
- Synaptopathy
- SYNGAP1-related intellectual disability
- Synkinesis
- Synucleinopathy
- SYT1-associated neurodevelopmental disorder