Template:Central nervous system disease

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Diseases of the nervous system, primarily CNS

Brain	* Encephalitis Viral encephalitis Herpesviral encephalitis Limbic encephalitis Encephalitis lethargica Cavernous sinus thrombosis Brain abscess Amoebic
Brain and spinal cord	* Encephalomyelitis Acute disseminated Meningitis Meningoencephalitis

Brain/
encephalopathy

Extrapyramidal and movement disorders	* Basal ganglia disease Parkinsonism PD Postencephalitic NMS NBIA PKAN Tauopathy PSP Striatonigral degeneration Hemiballismus HD OA Dyskinesia Dystonia Status dystonicus Spasmodic torticollis Meige's Blepharospasm Athetosis Chorea Choreoathetosis Myoclonus Myoclonic epilepsy Akathisia Tremor Essential tremor Intention tremor Restless legs Stiff-person
Dementia	* Tauopathy Alzheimer's Early-onset Primary progressive aphasia Frontotemporal dementia/Frontotemporal lobar degeneration Pick's Lewy bodies dementia Posterior cortical atrophy Vascular dementia
Mitochondrial disease	* Leigh syndrome

Inflammatory
Multiple sclerosis
For more detailed coverage, see Template:Demyelinating diseases of CNS

Episodic/
paroxysmal

Seizures and epilepsy	* Focal Generalised Status epilepticus For more detailed coverage, see Template:Epilepsy
Headache	* Migraine Cluster Tension For more detailed coverage, see Template:Headache
Cerebrovascular	* TIA Stroke For more detailed coverage, see Template:Cerebrovascular diseases
Other	* Sleep disorders For more detailed coverage, see Template:Sleep

* Intracranial hypertension

Other

* Brain herniation

Both/either

* Friedreich's ataxia

Ataxia–telangiectasia

* UMN only:

LMN only:
- Distal hereditary motor neuronopathies
- Spinal muscular atrophies
  - SMA
  - SMAX1
  - SMAX2
  - DSMA1
  - Congenital DSMA
  - Spinal muscular atrophy with lower extremity predominance (SMALED)
  - SMA-PCH
  - SMA-PME
- Progressive muscular atrophy
- Progressive bulbar palsy
  - Fazio–Londe
  - Infantile progressive bulbar palsy

both:
- Amyotrophic lateral sclerosis

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