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Ontology Browser

Parent Terms Term With Siblings Child Terms
cerebellar disease +     
ciliopathy +     
Alstrom syndrome  
Arima Syndrome 
Bardet-Biedl syndrome +   
Behrens Baumann Dust Syndrome 
Caroli disease +   
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 
Ciliary Motility Disorders +   
Dandy-Walker syndrome +   
Dykes Markes Harper Syndrome 
Dystonia with Cerebellar Atrophy 
Joubert syndrome +   
A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. (DO)
L-2-hydroxyglutaric aciduria  
Meckel syndrome +   
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 
primary cerebellar degeneration +   
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Stevenson-Carey Syndrome 
Subacute Cerebellar Degeneration 


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