neurodegeneration
central nervous system disease
Facial Onset Sensory Motor Neuropathy syndrome
medical condition
hereditary ataxia
neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
multiple system atrophy
neurodegenerative disorder characterized by autonomic failure, parkinsonism, cerebellar impairment and corticospinal signs, with a median survival of 6-9 years
amyotrophic neuralgia
human disease
Pick disease
rare neurodegenerative disorder, characterized by formation of Pick bodies
Huntington's disease-like syndrome
human disease
cerebral degeneration
human disease
motor neuron disease
group of neurological disorders affecting motor neurons
infantile cerebellar-retinal degeneration
neurodegenerative disease that is characterized by onset between ages 2 and 6 months of truncal hypotonia, athetosis, seizures, and ophthalmologic abnormalities, particularly optic atrophy and retinal degeneration
bovine spongiform encephalopathy
counterpart in cattle to variant Creutzfeldt-Jakob disease
amyotrophic lateral sclerosis
rare neurodegenerative disease with amyotrophy and progressive paralysis
Huntington's disease
rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
chronic traumatic encephalopathy
neurodegenerative disease caused by head injury