encephalopathy
central nervous system diseases located in the brain
cerebrovascular disease
artery disease that is characterized by dysfunction of the blood vessels supplying the brain
central nervous system cyst
human disease
hypothalamic disease
human disease
subarachnoid hemorrhage
bleeding into the subarachnoid space
bulbar syndrome
disease
Wernicke encephalopathy
presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves,
epilepsy
human neurological disease causing seizures
brain compression
Human disease
basal ganglia disease
brain disease that is characterized by dysfunction of the basal ganglia which help start and control movement
pituitary gland disease
endocrine disease
intracranial hypotension
human disease
Eastern equine encephalitis
horse disease
thalamic disease
class of human diseases involving the thalamus
intracranial hypertension
Human disease
transmissible spongiform encephalopathy
group of brain diseases induced by prion proteins
Japanese encephalitis
infection of the brain caused by the Japanese encephalitis virus
brainstem disease
disease
brain cancer
central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain
migraine
disorder resulting in recurrent moderate-severe headaches
cerebral palsy
group of permanent movement disorders that appear in early childhood
cerebellar disease
human disease
cerebral degeneration
human disease
cerebritis
Human disease
toxic encephalopathy
nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems
Disconnection syndrome
collection of neurological symptoms
Western equine encephalitis
Human disease
hepatic encephalopathy
brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood
encephalomalacia
Human disease
cerebral edema
human disease
movement disorders
clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
cerebral arteriovenous malformation
arteriovenous malformation that is located in the brain
akinetic mutism
brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness
hypoglycemic coma
human disease
cerebral toxoplasmosis
parasitic brain disease affecting humans
encephalitis
acute inflammation of the brain with flu-like symptoms
Murray Valley encephalitis
Human disease
Joubert syndrome
Joubert syndrome (JS) is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones
viral encephalitis transmitted by tick
any encephalitis transmited by tick
La Crosse encephalitis
Human disease
granulomatous amebic encephalitis
Human disease