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Ontology Browser

Term:
spinocerebellar ataxia type 2 (DOID:0050955)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant cerebellar ataxia, deafness and narcolepsy  
dentatorubral-pallidoluysian atrophy  
GRID2-related spinocerebellar ataxia 
hypomyelinating leukoencephalopathy 
Machado-Joseph disease +   
Microcephaly Pontocerebellar Hypoplasia Dyskinesia 
Olivopontocerebellar Atrophy 1 
Olivopontocerebellar Atrophy 3 
Olivopontocerebellar Atrophy II, Autosomal Recessive 
Olivopontocerebellar Atrophy V 
Spinocerebellar Ataxia 32 
Spinocerebellar Ataxia 41  
Spinocerebellar Ataxia 42  
Spinocerebellar Ataxia 42, Early-Onset, Severe, with Neurodevelopmental Deficits  
Spinocerebellar Ataxia 43  
spinocerebellar ataxia 44  
spinocerebellar ataxia 45  
spinocerebellar ataxia 46  
Spinocerebellar Ataxia 47  
Spinocerebellar Ataxia 48  
spinocerebellar ataxia type 1  
spinocerebellar ataxia type 10  
spinocerebellar ataxia type 11  
spinocerebellar ataxia type 12  
spinocerebellar ataxia type 13  
spinocerebellar ataxia type 14  
spinocerebellar ataxia type 15  
spinocerebellar ataxia type 17  
spinocerebellar ataxia type 18 
spinocerebellar ataxia type 19/22  
spinocerebellar ataxia type 2  
An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene. (DO)
spinocerebellar ataxia type 20 
spinocerebellar ataxia type 21  
spinocerebellar ataxia type 23  
spinocerebellar ataxia type 25 
spinocerebellar ataxia type 26  
spinocerebellar ataxia type 27  
spinocerebellar ataxia type 28  
spinocerebellar ataxia type 29  
spinocerebellar ataxia type 30 
spinocerebellar ataxia type 31  
spinocerebellar ataxia type 34  
spinocerebellar ataxia type 35  
spinocerebellar ataxia type 36  
spinocerebellar ataxia type 37  
spinocerebellar ataxia type 38  
spinocerebellar ataxia type 4  
spinocerebellar ataxia type 40  
spinocerebellar ataxia type 5  
spinocerebellar ataxia type 6  
spinocerebellar ataxia type 7  
spinocerebellar ataxia type 8  
Spinocerebellar Ataxia, X-Linked 1  
Spinocerebellar Atrophy with Pupillary Paralysis 

Synonyms
Exact Synonyms: OPCA2 ;   SCA2 ;   olivopontocerebellar atrophy 2 ;   olivopontocerebellar atrophy II ;   olivopontocerebellar atrophy, Holguin type ;   spinocerebellar ataxia 2 ;   spinocerebellar ataxia with slow eye movements ;   spinocerebellar ataxia, Cuban type ;   spinocerebellar atrophy 2 ;   spinocerebellar atrophy II ;   spinocerebellar degeneration with slow eye movements
Primary IDs: OMIM:183090
Alternate IDs: RDO:9003726
Definition Sources: https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-2

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