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Ontology Browser

Term:
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM (DOID:9000707)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Atrophy +     
brain disease +     
Acute Febrile Encephalopathy 
Agenesis of Corpus Callosum +   
Aicardi-Goutieres syndrome +   
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 Cysts +   
central nervous system origin vertigo 
Central Nervous System Vascular Malformations +   
cerebellar disease +   
cerebellar hypoplasia +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
chromosome 17p13.3 duplication syndrome  
Chronic Brain Damage +   
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
Congenital Cerebral Granulomas 
Crome Syndrome 
cystic echinococcosis  
Dandy-Walker syndrome +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
Drachtman Weinblatt Sitarz Syndrome 
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  
An autosomal recessive neurodevelopmental disorder characterized by severely delayed psychomotor development apparent soon after birth or in infancy, profound intellectual disability, poor or absent speech, and seizures. (OMIM)
epilepsy +   
GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME  
Headache Disorders +   
HEART AND BRAIN MALFORMATION SYNDROME  
hepatic encephalopathy +   
hereditary sensory neuropathy +   
heterophyiasis 
hypoglycemic coma 
hypothalamic disease +   
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 +   
lymphocytic choriomeningitis  
Median-Ulnar Nerve Communications 
Metabolic Brain Diseases +   
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
movement disease +   
muscular atrophy +   
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
neural tube defect +   
Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
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 Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY  
neurodevelopmental disorder with midbrain and hindbrain malformations  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
Neurodevelopmental Disorder with or without Autistic Features and/or Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
neuroschistosomiasis 
NFIA-related disorder  
Non-Lissencephalic Cortical Dysplasia 
paragonimiasis 
phaeohyphomycosis +  
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +   
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Schisis Association 
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
septooptic dysplasia +   
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
syndromic microphthalmia 3  
syndromic microphthalmia 6  
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  

Synonyms
Exact Synonyms: PEBAT
Primary IDs: OMIM:617193 ;   RDO:9001701

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