Parent term(s)
Term with siblings
akinetic mutism
alveolar echinococcosis
Athabaskan brainstem dysgenesis syndrome
basal ganglia disease +
baylisascariasis
brain cancer +
brain compression
brain edema
brain small vessel disease +
central nervous system origin vertigo
cerebellar disease +
cerebral degeneration +
cerebral palsy +
cerebritis
cerebrovascular disease +
complex cortical dysplasia with other brain malformations +
cortical dysplasia-focal epilepsy syndrome
cystic echinococcosis
diabetic encephalopathy
Eastern equine encephalitis
encephalitis +
encephalomalacia +
epilepsy +
familial febrile seizures +
frontotemporal dementia +
granulomatous amebic encephalitis
hepatic encephalopathy +
heterophyiasis
homocarnosinosis
hypoglycemic coma
hypothalamic disease +
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
intracranial hypertension +
intracranial hypotension
Japanese encephalitis
Joubert syndrome +
kernicterus
La Crosse encephalitis
low grade glioma +
lymphocytic choriomeningitis
MASA syndrome
migraine +
movement disease +
Murray Valley encephalitis
neuroschistosomiasis
paragonimiasis
PEHO syndrome
porencephaly
prion disease +
pseudobulbar palsy
severe congenital encephalopathy due to MECP2 mutation
sparganosis
tertiary neurosyphilis +
thalamic disease
toxocariasis
traumatic brain injury
Wernicke encephalopathy
West Nile encephalitis +
Western equine encephalitis
polymicrogyria +
akinetic mutism
alveolar echinococcosis
Athabaskan brainstem dysgenesis syndrome
basal ganglia disease +
baylisascariasis
brain cancer +
brain compression
brain edema
brain small vessel disease +
central nervous system origin vertigo
cerebellar disease +
cerebral degeneration +
cerebral palsy +
cerebritis
cerebrovascular disease +
complex cortical dysplasia with other brain malformations +
cortical dysplasia-focal epilepsy syndrome
cystic echinococcosis
diabetic encephalopathy
Eastern equine encephalitis
encephalitis +
encephalomalacia +
epilepsy +
familial febrile seizures +
frontotemporal dementia +
granulomatous amebic encephalitis
hepatic encephalopathy +
heterophyiasis
homocarnosinosis
hypoglycemic coma
hypothalamic disease +
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
intracranial hypertension +
intracranial hypotension
Japanese encephalitis
Joubert syndrome +
kernicterus
La Crosse encephalitis
low grade glioma +
lymphocytic choriomeningitis
MASA syndrome
migraine +
movement disease +
Murray Valley encephalitis
neuroschistosomiasis
paragonimiasis
PEHO syndrome
porencephaly
prion disease +
pseudobulbar palsy
severe congenital encephalopathy due to MECP2 mutation
sparganosis
tertiary neurosyphilis +
thalamic disease
toxocariasis
traumatic brain injury
Wernicke encephalopathy
West Nile encephalitis +
Western equine encephalitis
denotes an 'is-a' relationship