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Ontology Browser

Term:
Cerebelloparenchymal Disorder VI (DOID:9001075)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Arima Syndrome 
Bannayan-Riley-Ruvalcaba syndrome  
Behrens Baumann Dust Syndrome 
Cerebellar Degeneration-Related Autoantigen 3 
Cerebellar Granule Cell Hypertrophy and Megalencephaly 
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 
Cowden syndrome +   
Cowden-Like Syndrome  
Dandy-Walker syndrome +   
Dykes Markes Harper Syndrome 
Dystonia with Cerebellar Atrophy 
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15  
Graham Boyle Troxell Syndrome 
Joubert syndrome +   
L-2-hydroxyglutaric aciduria  
Megalencephaly with Thick Corpus Callosum, Cerebellar Atrophy, and Intellectual Disability  
Miller Fisher syndrome 
Multiple Basal Cell Carcinoma 
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 +   
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Proteus syndrome +   
Sacral Hemangiomas Multiple Congenital Abnormalities 
Stevenson-Carey Syndrome 
Subacute Cerebellar Degeneration 

Synonyms
Primary IDs: MESH:C563564 ;   RDO:0012789

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