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:
Central nervous system disease
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v
t
e
Diseases of the
nervous system
, primarily
CNS
Inflammation
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
Degenerative
Extrapyramidal
and
movement disorders
Basal ganglia disease
Parkinsonism
PD
Postencephalitic
NMS
PSP
CBD
NBIA
PKAN
Striatonigral degeneration
Hemiballismus
Huntington's disease
Olivopontocerebellar atrophy
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
Alzheimer's
Early-onset
Primary progressive aphasia
Frontotemporal dementia
/
Frontotemporal lobar degeneration
Lewy body dementia
Posterior cortical atrophy
Creutzfeldt–Jakob disease
Vascular dementia
Mitochondrial disease
Leigh syndrome
Demyelinating
Autoimmune
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
CSF
Intracranial hypertension
Hydrocephalus
Normal pressure hydrocephalus
Choroid plexus papilloma
Idiopathic intracranial hypertension
Cerebral edema
Intracranial hypotension
Other
Brain herniation
Reye syndrome
Hepatic encephalopathy
Toxic encephalopathy
Hashimoto's encephalopathy
Static encephalopathy
Both/either
Degenerative
SA
Friedreich's ataxia
Ataxia–telangiectasia
MND
UMN
only:
Primary lateral sclerosis
Pseudobulbar palsy
Hereditary spastic paraplegia
LMN
only:
Distal hereditary motor neuronopathies
Spinal muscular atrophies
SMA
SMAX1
SMAX2
DSMA1
Congenital DSMA
Spinal muscular atrophy with lower extremity predominance (SMALED)
SMALED1
SMALED2A
SMALED2B
SMA-PCH
SMA-PME
Progressive muscular atrophy
Progressive bulbar palsy
Fazio–Londe
Infantile progressive bulbar palsy
both:
Amyotrophic lateral sclerosis
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