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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
aceruloplasminemia  
Acute Febrile Encephalopathy 
agenesis of the corpus callosum with peripheral neuropathy  
akinetic mutism 
alveolar echinococcosis  
amblyopia +   
Athabaskan brainstem dysgenesis syndrome  
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
borna disease  
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Central Auditory Diseases +   
Central Nervous System Bacterial Infections +   
Central Nervous System Fungal Infections +   
central nervous system origin vertigo 
Central Nervous System Parasitic Infections +   
Central Nervous System Viral Diseases +   
cerebellar disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy  
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Childhood-Onset Neurodegeneration with Brain Atrophy  
Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
Chronic Brain Damage +   
Chronic Traumatic Encephalopathy 
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
Congenital Cerebral Granulomas 
Crome Syndrome 
cystic echinococcosis  
cysticercosis +  
dementia +   
demyelinating disease +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
encephalitis +   
encephalomalacia +   
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epidural abscess 
epilepsy +   
eye degenerative disease +   
eyelid degenerative disease +  
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
Headache Disorders +   
hepatic encephalopathy +   
hereditary ataxia +   
heterophyiasis 
Huntington's disease-like 2  
hydrocephalus +   
hypoglycemic coma 
hypothalamic disease +   
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
Infectious Encephalitis +   
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
lymphocytic choriomeningitis  
meningoencephalitis +   
Metabolic Brain Diseases +   
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
motor neuron disease +   
movement disease +   
multiple system atrophy +   
myelitis +   
myoclonic cerebellar dyssynergia +  
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
Nervous System Heredodegenerative Disorders +   
Nervous System Paraneoplastic Syndromes +   
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
Neuronal Intranuclear Inclusion Disease  
neuroschistosomiasis 
Non-Lissencephalic Cortical Dysplasia 
olivopontocerebellar atrophy +   
paragonimiasis 
PEHO syndrome  
Perimeningeal Infections +  
phaeohyphomycosis +  
Pick's disease  
plexopathy 
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
prion disease +   
A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with PRIONS. These diseases are characterized by conversion of a normal protein to a prion configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these incorrectly as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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 +   
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
secondary Parkinson disease +   
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Subacute Combined Degeneration  
Subdural Effusion 
synucleinopathy +   
tauopathy +   
TDP-43 Proteinopathies +   
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  

Synonyms
Exact Synonyms: Genetic Prion Diseases ;   Inherited Human Transmissible Spongiform Encephalopathies ;   Prion Induced Disorder ;   Prion Protein Disease ;   Prion Protein Diseases ;   Prion disease pathway ;   Prion-Associated Disorders ;   Prion-Induced Disorders ;   Spongiform Encephalopathy ;   Transmissible Dementia ;   Transmissible Dementias ;   Transmissible Spongiform Encephalopathies ;   Transmissible Spongiform Encephalopathy ;   prion diseases
Related Synonyms: Prion Disease, Susceptibility To
Primary IDs: MESH:D017096 ;   RDO:0005908
Xrefs: ICD10CM:A81.9 ;   NCI:C128346
Definition Sources: http://en.wikipedia.org/wiki/Prion "DO", http://www.cdc.gov/ncidod/dvrd/prions/ "DO", MESH:D017096

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