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Ontology Browser
Term:
Spongiform Encephalopathy with Neuropsychiatric Features (DOID:9005780)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
Alexander disease  
Canavan disease  
Cerebral Amyloidosis with Spongiform Encephalopathy +   
Cerebrocortical Degeneration of Infancy 
childhood spinal muscular atrophy +   
Chromosome 18 Pericentric Inversion 
chronic wasting disease 
Cockayne syndrome +   
cognitive disorder +   
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
Creutzfeldt-Jakob disease +   
DEVELOPMENTAL DELAY, BEHAVIORAL ABNORMALITIES, AND NEUROPSYCHIATRIC DISORDERS  
DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES  
DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES  
developmental disorder of mental health +   
dissociative disorder +  
Distal Renal Tubular Acidosis, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies 
dysphoria 
Dystonia Musculorum Deformans +   
eating disorder +   
Elimination Disorders +   
factitious disorder +  
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
Familial Partial Lipodystrophy Type 7  
fatal familial insomnia  
Gerstmann-Straussler-Scheinker syndrome  
Gilles de la Tourette syndrome +   
Hereditary Central Nervous System Demyelinating Diseases +   
Hereditary Optic Atrophies +   
hereditary sensory neuropathy +   
Huntington's disease +   
Huntington's disease-like 1  
Huntington's disease-like 2  
Huntington's Disease-Like Syndrome  
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
impulse control disorder +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES  
internalizing disorder 
Kennedy's disease  
kuru  
Lafora disease +   
Leukoencephalomyelopathy  
mitochondrial DNA depletion syndrome 6  
Motor Disorders +   
motor peripheral neuropathy +   
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
myotonia congenita +   
myotonic dystrophy type 1 +   
neuroacanthocytosis +   
Neurodevelopmental Disorders +   
neurofibromatosis +   
neurogenic scapuloperoneal syndrome Kaeser type  
neuronal ceroid lipofuscinosis +   
Opticocochleodentate Degeneration 
pantothenate kinase-associated neurodegeneration  
PCWH syndrome  
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
personality disorder +   
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary cerebellar degeneration +   
Progressive Psychomotor Deterioration  
Schizophrenia Spectrum and Other Psychotic Disorders +   
scrapie  
sexual health disorder +   
sleep disorder +   
somatoform disorder +   
spinal muscular atrophy with lower extremity predominant +   
Spongiform Encephalopathy with Neuropsychiatric Features  
substance-related disorder +   
syndromic microphthalmia 10 
Trauma and Stressor Related Disorders +   
tuberous sclerosis +   
Unverricht-Lundborg syndrome +   
variant Creutzfeldt-Jakob disease +  
Wilson disease +   
X-linked Epilepsy 2 with or without Impaired Intellectual Development and Dysmorphic Features  
X-Linked Intellectual Developmental Disorders +   

Synonyms
Primary IDs: MESH:C564678
Alternate IDs: MIM:606688

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