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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
cerebellar disease +     
Nerve Degeneration +     
Arima Syndrome 
Behrens Baumann Dust Syndrome 
Cerebellar Degeneration-Related Autoantigen 3 
cerebellar hypoplasia +   
Cerebellar Neoplasms +   
Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
Cerebelloparenchymal Disorder VI 
Dandy-Walker syndrome +   
Dykes Markes Harper Syndrome 
Dystonia with Cerebellar Atrophy 
Glycosylphosphatidylinositol Biosynthesis Defect 15  
Joubert syndrome +   
L-2-hydroxyglutaric aciduria  
Megalencephaly with Thick Corpus Callosum, Cerebellar Atrophy, and Intellectual Disability  
Miller Fisher syndrome 
Neurodevelopmental Disorder with Hypotonia and Cerebellar Atrophy, with or without Seizures  
Paraneoplastic Cerebellar Degeneration 
pontocerebellar hypoplasia +   
Porencephaly Cerebellar Hypoplasia Malformations 
PORETTI-BOLTSHAUSER SYNDROME  
primary cerebellar degeneration +   
Retrograde Degeneration  
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal  
Stevenson-Carey Syndrome 
Striatal Degeneration, Autosomal Dominant +   
Subacute Cerebellar Degeneration 
Subacute Combined Degeneration  
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)  
Wallerian Degeneration +   

Synonyms
Primary IDs: MESH:C535352

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