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Ontology Browser
Term:
Spastic Pseudosclerosis (DOID:9004579)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
brain disease +     
neurodegenerative disease +     
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  
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 origin vertigo 
CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS  
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  
demyelinating disease +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
encephalitis +   
encephalomalacia +   
Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission +   
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, 9  
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  
epilepsy +   
eye degenerative disease +   
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
Headache Disorders +   
hepatic encephalopathy +   
hereditary ataxia +   
heterophyiasis 
Huntington's disease-like 2  
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  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES  
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
lymphocytic choriomeningitis  
Metabolic Brain Diseases +   
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
motor neuron disease +   
movement disease +   
multiple system atrophy +   
myoclonic cerebellar dyssynergia +  
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
Nervous System Heredodegenerative Disorders +   
Nervous System Paraneoplastic Syndromes +   
Neurodegeneration with Ataxia and Late-Onset Optic Atrophy  
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE  
NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
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  
phaeohyphomycosis +  
plexopathy 
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
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 +   
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: Corticopallidodegeneration ;   Disseminated Encephalomyelopathy
Primary IDs: MESH:C563024
Alternate IDs: OMIM:270900

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