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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)
Parent Terms Term With Siblings Child Terms
adjustment disorder  
Alexander disease  
anxiety disorder +   
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 disorder of mental health +   
dissociative disorder +  
Distal Renal Tubular Acidosis, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies 
Dystonia Musculorum Deformans +   
eating disorder +   
Elimination Disorders +   
factitious disorder +  
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
fatal familial insomnia  
Fragile Site 16p12 
gender identity disorder +  
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 Abnormal Behavior, Microcephaly, and Short Stature  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES  
Kennedy's disease  
kuru  
Lafora disease  
Leukoencephalomyelopathy  
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
Luscan-Lumish syndrome  
Mental Retardation, X-Linked +   
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 +   
paraphilia disorder +  
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 disorder +   
sleep disorder +   
somatoform disorder +   
spinal muscular atrophy with lower extremity predominance +   
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, with Variable Learning Disabilities and Behavior Disorders  

Synonyms
Primary IDs: MESH:C564678 ;   RDO:0013552
Alternate IDs: OMIM:606688

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