• • disease
    • human disease
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      • nervous system disorder
        • Angelman syndrome
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        • atactic disorder
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        • ATP1A3-associated neurological disorder
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        • autoimmune disorder of the nervous system
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        • Balint syndrome
        • Barre-Lieou syndrome
        • Behr syndrome
        • central nervous system disorder
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        • central nervous system malformation
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        • cerebellar hypoplasia-tapetoretinal degeneration syndrome
        • chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
        • congenital nervous system disorder
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        • cranial nerve neuropathy
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        • developmental disability
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        • diplegia of upper limb
        • drug-induced akathisia
        • drug-induced dyskinesia
        • exercise-induced malignant hyperthermia
        • FOXG1 syndrome
        • Gerstmann syndrome
        • idiopathic recurrent stupor
        • infectious disorder of the nervous system
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        • inherited nervous system cancer-predisposing syndrome
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        • KIF1A related neurological disorder
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        • locked-in syndrome
        • Minamata disease
        • movement disorder
          • arthrogryposis
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          • behavioral variant of frontotemporal dementia
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          • benign paroxysmal tonic upgaze of childhood with ataxia
          • benign shuddering attacks
          • brain-lung-thyroid syndrome
          • cerebellar ataxia
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          • childhood-onset benign chorea with striatal involvement
          • childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
          • choreatic disease
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          • chronic tic disorder
          • corticobasal syndrome
          • dyskinesia with orofacial involvement, autosomal dominant
          • dystonic disorder
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          • epilepsy with myoclonic absences
          • essential tremor
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          • extrapyramidal and movement disease
          • familial congenital mirror movements
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          • frontotemporal dementia with motor neuron disease
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          • hereditary geniospasm
          • Huntington disease
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          • Huntington disease-like 3
          • Huntington disease-like syndrome due to C9ORF72 expansions
          • hyperekplexia
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          • infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
          • inherited Creutzfeldt-Jakob disease
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          • intellectual disability-hyperkinetic movement-truncal ataxia syndrome
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          • juvenile myoclonic epilepsy
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          • kuru
          • Lafora disease
          • lingual-facial-buccal dyskinesia
          • motor stereotypies
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          • multiple system atrophy
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          • neuroacanthocytosis
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          • neurodegeneration with brain iron accumulation
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          • neuronal intranuclear inclusion disease
          • opsoclonus-myoclonus syndrome
          • primary myoclonus
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          • primary orthostatic tremor
          • progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
          • progressive myoclonic epilepsy type 7
          • progressive non-fluent aphasia
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          • progressive supranuclear palsy
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          • proximal myopathy with extrapyramidal signs
          • psychogenic movement disorders
          • Sandifer syndrome
          • sensorineural hearing loss-early graying-essential tremor syndrome
          • SLC6A3-related dopamine transporter deficiency syndrome
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          • spinal muscular atrophy-progressive myoclonic epilepsy syndrome
          • Tourette syndrome
          • transient tic disorder
          • tremor-nystagmus-duodenal ulcer syndrome
          • Unverricht-Lundborg syndrome
          • variably protease-sensitive prionopathy
        • multiple sclerosis variant
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        • myalgic encephalomeyelitis/chronic fatigue syndrome
        • neonatal brainstem dysfunction
        • nervous system injury
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        • nervous system neoplasm
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        • neurocutaneous syndrome
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        • neurodevelopmental disorder
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        • neuroendocrine disorder
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        • neuroleptic malignant syndrome
        • neurological pain disorder
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        • neuromuscular disease
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        • neuromyelitis optica
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        • neuronitis
        • neuroocular syndrome
        • neurosarcoidosis
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        • neurovascular disorder
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        • neurovascular malformation
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        • oculocerebrocutaneous syndrome
        • pachygyria-intellectual disability-epilepsy syndrome
        • paraneoplastic neurologic syndrome
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        • PEHO-like syndrome
        • perceptual disorders
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        • perineural cyst
        • periodic paralysis
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        • peripheral nervous system disorder
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        • persistent idiopathic facial pain
        • porencephaly-cerebellar hypoplasia-internal malformations syndrome
        • prepubertal anorexia nervosa
        • primary orthostatic disorder
        • primary orthostatic hypotension
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        • qualitative or quantitative protein defects in neuromuscular diseases
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        • radiculitis
        • restless legs syndrome
        • retinal disorder
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        • sensory ganglionopathy
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        • serotonin syndrome
        • sleep disorder
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        • specific learning disability
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        • spontaneous periodic hypothermia
        • stiff-person syndrome
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        • Sydenham chorea
        • symmetrical thalamic calcifications
        • synaptopathy
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        • toxic encephalopathy
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        • tubulinopathy
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        • Wallerian degeneration
        • wet beriberi
        • Worster-Drought syndrome
      • nutritional disorder
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      • obstetric disorder
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      • occupational disorder
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      • otorhinolaryngologic disease
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      • perinatal disease
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      • poisoning
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      • post-bacterial disorder
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      • post-COVID-19 disorder
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      • post-infectious disorder
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      • post-viral disorder
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      • psychiatric disorder
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      • radiation-induced disorder
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      • reproductive system disorder
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      • respiratory system disorder
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      • syndromic disease
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      • ulcer disease
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      • upper digestive tract disorder
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      • urinary system disorder
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    • non-human animal disease
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  • injury
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