Parent term(s)
brain disease
+
Term with siblings
movement disease +
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
+
Murray Valley encephalitis
neuroschistosomiasis
paragonimiasis
PEHO syndrome
polymicrogyria
+
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
Child term(s)
benign shuddering attacks
choreatic disease
+
congenital mirror movement disorder
dopamine transporter deficiency syndrome
+
dystonia
+
essential tremor
+
extrapyramidal and movement disease
infantile parkinsonism-dystonia 2
lingual-facial-buccal dyskinesia
neurodevelopmental disorder with involuntary movements
Parkinsonism
+
progressive supranuclear palsy
Stiff-Person syndrome
X-linked parkinsonism-spasticity syndrome
denotes an 'is-a' relationship