Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
brain disease +     
thalamic disease +     
Acute Febrile Encephalopathy 
akinetic mutism 
alveolar echinococcosis 
amblyopia +   
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Central Auditory Diseases +   
central nervous system origin vertigo 
cerebellar disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
chromosome 1p32-p31 deletion syndrome  
Chronic Brain Damage +   
Colpocephaly  
complex cortical dysplasia with other brain malformations +   
Crome Syndrome 
cystic echinococcosis 
dementia +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
encephalitis +   
encephalomalacia +   
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epilepsy +   
Granulomas, Congenital Cerebral 
Headache Disorders +   
hepatic encephalopathy +   
heterophyiasis 
hydrocephalus +   
hypoglycemic coma 
hypothalamic disease +   
Neoplastic, inflammatory, infectious, and other diseases of the hypothalamus. Clinical manifestations include appetite disorders; AUTONOMIC NERVOUS SYSTEM DISEASES; SLEEP DISORDERS; behavioral symptoms related to dysfunction of the LIMBIC SYSTEM; and neuroendocrine disorders.
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
lymphocytic choriomeningitis  
Metabolic Brain Diseases +   
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
movement disease +   
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
neuroschistosomiasis 
Non-Lissencephalic Cortical Dysplasia 
olfactory nerve disease +   
paragonimiasis 
phaeohyphomycosis +  
Postnatal Progressive Microcephaly with Seizures and Brain Atrophy  
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +  
Rajab Syndrome  
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
tertiary neurosyphilis +  
Thalamic Degeneration Symmetrical Infantile 
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  

Synonyms
Exact Synonyms: Hypothalamic Adenohypophyseal Disorders ;   Hypothalamic Diseases ;   Hypothalamic Dysfunction Syndrome ;   Hypothalamic Dysfunction Syndromes ;   Hypothalamic Dysinhibition Syndrome ;   Hypothalamic Dysinhibition Syndromes ;   Hypothalamic Neurohypophyseal Disorders ;   Hypothalamic Overactivity Syndrome ;   Hypothalamic Overactivity Syndromes ;   Hypothalamic Pseudopuberties ;   Hypothalamic Pseudopuberty ;   Hypothalamic-Adenohypophyseal Disorder ;   Hypothalamic-Neurohypophyseal Disorder ;   Pituitary Diencephalic Syndrome ;   Pituitary Diencephalic Syndromes
Primary IDs: MESH:D007027
Alternate IDs: RDO:0002940

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.